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1. WO2020109039 - PESTICIDAL COMPOUNDS

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Pesticidal compounds

Description

Invertebrate pests and in particular insects, arachnids and nematodes destroy growing and harvested crops and attack wooden dwelling and commercial structures, thereby causing large economic loss to the food supply and to property. Accordingly, there is an ongoing need for new agents for combating invertebrate pests.

Carbamoylated and thiocarbamoylated oxime derivatives are known for pesticidal use, for example, in patent publications WO 2016/156076, semi-carbazones and thiosemicarbazones derivatives are known for pesticidal use in patent publication WO 2016/1 16445.

Due to the ability of target pests to develop resistance to pesticidally-active agents, there is an ongoing need to identify further compounds, which are suitable for combating invertebrate pests such as insects, arachnids and nematodes. Furthermore, there is a need for new com pounds having a high pesticidal activity and showing a broad activity spectrum against a large number of different invertebrate pests, especially against difficult to control insects, arachnids and nematodes.

It is therefore an object of the present invention to identify and provide compounds, which exhibit a high pesticidal activity and have a broad activity spectrum against invertebrate pests.

It has been found that these objects can be achieved by substituted bicyclic compounds of formula I, as depicted and defined below, including their stereoisomers, their salts, in particu lar their agriculturally or veterinarily acceptable salts, their tautomers and their N-oxides.

In a first aspect, the present invention relates to the compounds of formula I,


(b

wherein

A1 is N or CRA1;

A2 is N or CRA2;

A3 is N or CRA3;

wherein at least one of the A1, A2, A3 is N;

B1 is N or CRB1; preferably B1 is CRB1;

B2 is N or CRB2; preferably B2 is CRB2;

B3 is N or CRB3; preferably B3 is CRB3;

RA1, RA2 , and RA3 independently of each other are selected from H, halogen, N3, OH, CN, NO2, -SCN, -SF5, Ci-C6-alkyl, Ci-C6-alkoxy, C2-C6-alkenyl, tri-Ci-C6-al- kylsilyl, C2-C6-alkynyl, Ci-C6-alkoxy-Ci-C4-alkyl, Ci-C6-alkoxy-Ci-C4-alkoxy, C3- C6-cycloalkyl, C3-C6-cycloalkoxy, C3-C6-cycloalkyl-Ci-C4-alkyl, Ci-C4-alkyl-C3-C6- cycloalkoxy, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with halogen,

C(=0)-0Ra, NRbRc, Ci-C6-alkylene-NRbRc, 0-Ci-C6-alkylene-NRbRc, Ci-C6-al- kylene-CN, NH-Ci-C6-alkylene-NRbRc, C(=0)-NRbRc, C(=0)-Rd, S02NRbRc, or S(=0)mRe, phenyl, phenoxy, phenylcarbonyl, phenylthio, or -CH2-phenyl, wherein the phenyl rings are unsubstituted or substituted with Rf;

RB1, RB2, and RB3, independently of each other are H, halogen, N3, OH, CN, NO2, - SCN, -SF5, Ci-C6-alkyl, Ci-C6-alkoxy, C2-C6-alkenyl, tri-Ci-C6-alkylsilyl, C2-C6-al- kynyl, Ci-C6-alkoxy-Ci-C4-alkyl, Ci-C6-alkoxy-Ci-C4-alkoxy, C3-C6-cycloalkyl, C3- C6-cycloalkoxy, C3-C6-cycloalkyl-Ci-C4-alkyl, Ci-C4-alkyl-C3-C6-cycloalkoxy, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with halogen,

C(=0)-0Ra, NRbRc, Ci-C6-alkylene-NRbRc, 0-Ci-C6-alkylene-NRbRc, Ci-C6-alkylene- CN, NH-Ci-C6-alkylene-NRbRc, C(=0)-NRbRc, C(=0)-Rd, S02NRbRc, or

S(=0)mRe, phenyl, phenoxy, phenylcarbonyl, phenylthio, or -CH2-phenyl, wherein the phenyl rings are unsubstituted or substituted with Rf;

Q is -N=C(X)-, -N(R2)-C(=NR)-, or -N(R2)-C(=S)-, -C(R4R5)-0-, -C(=0)-0-, - S(=0)m-C(R7R8)-, -N(R2)-S(=0)m-, -N(R2)-C(R9R10)-, -C(=0)-C(R19R20)-, -N(R2)- C(=0)-, -C(R13R14)-C(R15R16)-, or -C(R17)=C(R18)-; wherein Ar is bound to either side of Q;

X is identical or different, H, halogen, SR7, OR8, N(R3)2, -CR4=N(OCH3), CN, Ci-C6- alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C3-C6-cycloalkyl, wherein the alkyl, alkenyl, alkynyl and cycloalkyl moieties are unsubstituted or substituted with halogen; phenyl, or -CH2-phenyl, wherein the phenyl rings are unsubstituted or substituted with Rf;

R is identical or different, H, CN, Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C3-C6- cycloalkyl, wherein the alkyl, alkenyl, alkynyl and cycloalkyl moieties are unsubstituted or substituted with halogen,

SR7, OR8, N(R3)2, phenyl, or -CH2-phenyl, wherein the phenyl rings are unsubstituted or substituted with Rf;

R2 is H, Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, Ci-C6-alkoxy-Ci-C4-alkyl, C3-C6- cycloalkyl, C3-C6-cycloalkyl-Ci-C4-alkyl, C3-C6-cycloalkoxy-Ci-C4-alkyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with halogen,

C(0)-0Ra, Ci-C6-alkylen-NRbRc, Ci-C6-alkylen-CN, C(0)-NRbRc, C(0)-Rd, S02NRbRc, S(=0)mRe, phenyl, or -CH2-phenyl, wherein the phenyl rings are unsubstituted or substituted with Rf;

R3 is H, Ci-C6-alkyl, Ci-C6-alkoxy, C2-C6-alkenyl, C2-C6-alkynyl, Ci-C6-alkoxy-Ci-C4- alkyl, C3-C6-cycloalkyl, C3-C6-cycloalkyl-Ci-C4-alkyl, or C3-C6-cycloalkoxy-Ci-C4- alkyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with halogen,

Ci-C6-alkylene-CN, phenyl, or -Chh-phenyl, wherein the phenyl rings are unsubstituted or substituted with Rf;

R4, R5, R7, R8, R9, R10, R13, R14, R15, R16, R17, R18, R19, R20 are, identical or different, H, halogen, Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, Ci-C6-alkoxy-Ci-C4-alkyl, C3-C6-cycloalkyl, C3-C6-cycloalkyl-Ci-C4-alkyl, C3-C6-cycloalkoxy-Ci-C4-alkyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with halogen,

C(=0)-0Ra, Ci-C6-alkylene-NRbRc, Ci-C6-alkylene-CN, C(=0)-NRbRc, C(=0)-Rd, S02NRbRc, S(=0)mRe, phenyl, or -CH2-phenyl, wherein the phenyl rings are unsubstituted or substituted with Rf;

R6 is H, Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, Ci-C6-alkoxy-Ci-C4-alkyl, C3-C6- cycloalkyl, C3-C6-cycloalkyl-Ci-C4-alkyl, C3-C6-cycloalkoxy-Ci-C4-alkyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with halogen,

C(=0)-0Ra, Ci-C6-alkylene-NRbRc, Ci-C6-alkylene-CN, C(=0)-NRbRc, C(=0)-Rd, S02NRbRc, S(=0)mRe, phenyl, -CH2-C(=0)-0Ra, or -CH2-phenyl, wherein the phenyl rings are unsubstituted or substituted with Rf;

Ar is phenyl or 5- or 6-membered hetaryl, which are unsubstituted or substituted with RAr, wherein

RAr is halogen, N3, OH, CN, NO2, -SON, -SF5, Ci-Ce-alkyl, Ci-Ce-alkoxy, C2-C6- alkenyl, tri-Ci-C6-alkylsilyl, C2-C6-alkynyl, Ci-C6-alkoxy-Ci-C4-alkyl, Ci-C6-alkoxy- Ci-C4-alkoxy, C3-C6-cycloalkyl, C3-C6-cycloalkoxy, C3-C6-cycloalkyl-Ci-C4-alkyl, C3-C6-cycloalkoxy-Ci-C4-alkyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with halogen, C(=0)-0Ra, NRbRc, Ci-C6-alkylene-NRbRc, 0-Ci-C6-alkylene-NRbRc, Ci-C6- alkylene-CN, NH-Ci-C6-alkylene-NRbRc, C(=0)-NRbRc, C(=0)-Rd, S02NRbRc, or

S(=0)mRe, phenyl, phenoxy, phenylcarbonyl, phenylthio or -Chh-phenyl, wherein phenyl rings are unsubstituted or substituted with Rf;

R1 is a moiety of formula Y-Z-T-R11 or Y-Z-T-R12; wherein

Y is -CRya=N-, wherein the N is bound to Z;

-NRyc-C(=0)-, wherein C(=0) is bound to Z; or

-NRyc-C(=S)-, wherein C(=S) is bound to Z;

Z is a single bond;

-NRzc-C(=0)-, wherein C(=0) is bound to T;

-NRZC-C(=S)-, wherein C(=S) is bound to T;

-N=C(S-Rza)-, wherein T is bound to the carbon atom;

-0-C(=0)-, wherein T is bound to the carbon atom; or

-NRzc-C(S-Rza)=, wherein T is bound to the carbon atom;

T is O, N or N-RT;

R11 is Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, Ci-C6-alkoxy-Ci-C4-alkyl, C3-C6- cycloalkyl, C3-C6-cycloalkyl-Ci-C4-alkyl, Ci-C4-alkyl-C3-C6-cycloalkoxy, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with halogen,

Ci-C6-alkylene-NRbRc, Ci-C6-alkylene-CN, C(=0)-NRbRc, C(=0)-Rd, aryl, aryl-carbonyl, aryl-Ci-C4-alkyl, aryloxy-Ci-C4-alkyl, heteroaryl, carbonyl- heteroaryl, heteroaryl-Ci-C4-alkyl or heteroaryloxy-Ci-C4-alkyl, wherein the phenyl rings are unsubstituted or substituted with R9 and wherein the heteroaryl is a 5- or 6-membered monocyclic heteroaryl or a 8-, 9- or 10- membered bicyclic heteroaryl;

R12 is a radical of the formula A1;


wherein # indicates the point of attachment to T ;

R121, R122, R123 are, identical or different, H, halogen, Ci-C6-alkyl, C2-C6- alkenyl, C2-C6-alkynyl, Ci-C6-alkoxy-Ci-C4-alkyl, Ci-C6-alkoxy, C2-C6-al- kenyloxy, C2-C6-alkynyloxy, Ci-C6-alkoxy-Ci-C4-alkoxy, C1-C6- alkylcarbonlyoxy, Ci-C6-alkenylcarbonlyoxy, C3-C6- cycloalkylcarbonlyoxy, wherein the alkyl, alkoxy, alkenyl, alkenyloxy, alkynyl, alkynyloxy and cycloalkyl moieties are unsubstituted or substituted with halogen, or NRbRc, or one of R121, R122, R123 may also be oxo ;

R124 is H, Ci-C6-alkyl, Ci-C6-alkoxy-Ci-C4-alkyl, Ci-C6-alkoxy, or C2-C6- alkenyloxy, wherein the alkyl, alkoxy, alkenyl and alkenyloxy moieties are unsubstituted or substituted with halogen;

and where

Rya is H, halogen, Ci-C6-alkyl, Ci-C6-alkoxy, C2-C6-alkenyl, C2-C6-alkynyl, Ci- C6-alkoxy-Ci-C4-alkyl, C3-C6-cycloalkyl, Ci-C4-alkyl-C3-C6-cycloalkyl, C1-C4- alkyl-C3-C6-cycloalkoxy, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with halogen,

C(=0)-0Ra, Ci-C6-alkylene-NRbRc, Ci-C6-alkylene-CN, C(=0)-NRbRc, C(=0)-Rd, S02NRbRc, S(=0)mRe, phenyl, or -CH2-phenyl, wherein the phenyl rings are unsubstituted or substituted with Rf;

Ryc, Rzc are, identical or different, H, Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, Ci-C4-alkyl-Ci-C6-alkoxy, C3-C6-cycloalkyl, Ci-C4-alkyl-C3-C6-cycloalkyl, or Ci-C4-alkyl-C3-C6-cycloalkoxy, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with halogen;

RT is H, Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, Ci-C4-alkyl-Ci-C6-alkoxy, C3- C6-cycloalkyl, C3-C6-cycloalkyl-Ci-C4-alkyl, C3-C6-cycloalkoxy-Ci-C4-alkyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with halogen,

C(=0)-0Ra, Ci-C6-alkylene-NRbRc, Ci-C6-alkylene-CN, C(=0)-NRbRc, C(=0)-Rd, SC>2NRbRc, S(=0)mRe, phenyl, or -CH2-phenyl, wherein the phenyl rings are unsubstituted or substituted with Rf;

Rzc together with RT if present, may form Ci-C6-alkylene or a linear C2-C6- alkenylene group, where in the linear Ci-C6-alkylene and the linear C2-C6- alkenylene a CH2 moiety may be replaced by a carbonyl or a C=N-R' and/or wherein 1 or 2 CH2 moieties may be replaced by O or S and/or wherein the linear Ci-C6-alkylene and the linear C2-C6-alkenylene may be unsubstituted or substituted with Rh;

Rza is H, Ci-C6-alkyl, Ci-C6-alkoxy, C2-C6-alkenyl, tri-Ci-C6-alkylsilyl, C2-C6- alkynyl, Ci-C4-alkyl-Ci-C6-alkoxy, C3-C6-cycloalkyl, Ci-C4-alkyl-C3-C6- cycloalkoxy, Ci-C4-alkyl-C3-C6-cycloalkyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with halogen,

Ci-C6-alkylene-NRbRc, Ci-C6-alkylene-CN, C(=0)-NRbRc, C(=0)-Rd, phenyl,

phenylcarbonyl, or -Chh-phenyl, wherein the phenyl rings are unsubstituted or substituted with Rf;

Rza together with RT if present, may form Ci-C6-alkylene or a linear C2-C6- alkenylene group, where in the linear Ci-C6-alkylene and the linear C2-C6- alkenylene a CH2 moiety may be replaced by a carbonyl or a C=N-R' and/or wherein 1 or 2 CH2 moieties may be replaced by O or S and/or wherein the linear Ci-C6-alkylene and the linear C2-C6-alkenylene may be unsubstituted or substituted with Rh;

Ra, Rb and Rc are, identical or different, H, Ci-C6-alkyl, Ci-C6-alkoxy, C2-C6- alkenyl, C2-C6-alkynyl, Ci-C6-alkoxy-Ci-C4-alkyl, C3-C6-cycloalkyl, C3-C6- cycloalkyl-Ci-C4-alkyl, C3-C6-cycloalkoxy-Ci-C4-alkyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are

unsubstituted or substituted with halogen,

Ci-C6-alkylene-CN, phenyl, or -Chh-phenyl, wherein the phenyl rings are unsubstituted or substituted with Rf;

Rb and Rc together with the nitrogen they are attached may form 5- or 6- membered saturated, partially or fully unsaturated heterocyclic ring;

Rd is H, Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, Ci-C6-alkoxy-Ci-C4-alkyl, C3- C6-cycloalkyl, C3-C6-cycloalkyl-Ci-C4-alkyl, C3-C6-cycloalkoxy-Ci-C4-alkyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with halogen,

phenyl, or -Chh-phenyl, wherein the phenyl rings are unsubstituted or substituted with Rf;

Re is Ci-C6-alkyl, C3-C6-cycloalkyl, C3-C6-cycloalkyl-Ci-C4-alkyl, wherein the alkyl, cycloalkyl moieties are unsubstituted or substituted with halogen, phenyl and -Chh-phenyl, wherein the phenyl rings are unsubstituted or substituted with Rf;

Rf is halogen, N3, OH, CN, NO2, -SCN, -SF5, Ci-C6-alkyl, Ci-C6-alkoxy, C2-C6- alkenyl, tri-Ci-C6-alkylsilyl, C2-C6-alkynyl, Ci-C6-alkoxy-Ci-C4-alkyl, C1-C6- alkoxy-Ci-C4-alkoxy, C3-C6-cycloalkyl, C3-C6-cycloalkoxy, C3-C6-cycloalkyl- Ci-C4-alkyl, C3-C6-cycloalkoxyx-Ci-C4-alkyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with halogen,

C(=0)-0Ra, NRbRc, Ci-C6-alkylene-NRbRc, 0-Ci-C6-alkyiene-NRbRc, Ci-C6-alkylene-CN, NH-Ci-C6-alkylene-NRbRc, C(=0)-NRbRc, C(=0)-Rd, S02NRbRc, or S(=0)mRe;

R9 is halogen, N3, OH, CN, NO2, -SCN, -SF5, Ci-C6-alkyl, Ci-C6-alkoxy, C2-C6- alkenyl, tri-Ci-C6-alkylsilyl, C2-C6-alkynyl, Ci-C6-alkoxy-Ci-C4-alkyl, C1-C6- alkoxy-Ci-C4-alkoxy, C3-C6-cycloalkyl, C3-C6-cycloalkoxy, C3-C6-cycloalkyl- Ci-C4-alkyl, C3-C6-cycloalkoxy-Ci-C4-alkyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with halogen,

C(=0)-ORa, NRbRc, Ci-C6-alkylene-NRbRc, 0-Ci-C6-alkylene-NRbRc, Ci-C6-alkylene-CN, NH-Ci-C6-alkylene-NRbRc, C(=0)-NRbRc, C(=0)-Rd, S02NRbRc, or S(=0)mRe;

Rh is halogen, OH, Ci-C6-alkyl, C3-C6-cycloalkyl, or CN;

m is 0, 1 , or 2;

and the N-oxides, stereoisomers, tautomers and agriculturally or veterinarily acceptable salts thereof.

Moreover, the present invention also relates to processes and intermediates for preparing compounds of formula I and to active compound combinations comprising them. Moreover, the present invention relates to agricultural or veterinary compositions comprising the compounds of formula I, and to the use of the compounds of formula I or compositions comprising them for combating or controlling invertebrate pests and/or for protecting crops, plants, plant propagation material and/or growing plants from attack and/or infestation by invertebrate pests. The present invention also relates to methods of applying the compounds of formula I. Furthermore, the present invention relates to seed comprising compounds of formula I. Wherein the compounds of formula I includes N-oxides, stereoisomers, tautomers and agriculturally or veterinarily acceptable salts thereof.

With due modification of the starting compounds, the compounds of formula I can be prepared by procedures as given in below schemes.

Compounds of the formula S1-2 can be prepared in amide coupling reactions between an amine (ArNHR2) and compounds of the formula S1-1 using a coupling reagent such as HATU as described by, for example, Tobinaga, et al WO 2018/021447 (Scheme 1 ).

Alternatively compounds of the formula S1-1 can be pre-activated as an acid chloride by reaction with, for example, SOCI2, prior to reaction with an amine (ArNHR2) in the presense of a base (e.g. Et3N) to form compounds of the formula S1-2. Compounds of the formula S1-3 can, in turn, be prepared by reaction of compounds of the formula S1-2 with a thionating reagent such at P2S5 as described by, for example, Carroll et al, WO 2008/130953.

Compounds of the formula S1-4 can be synthesized by reaction of compounds of the formula S1-2 with a reducing agent such as BHs SMe2 as described by, for example, Chen et al, WO 2009/135299.

Scheme 1


S1-1 S1-2 S1-3

Compounds of the formula S2-2 can be prepared from compounds of the formula S2-1 by reaction with, for example, hydroxylamine hydrochloride in the presence of a base (e.g. NaOH, pyridine, triethylamine, K2CO3, NaH) as described by, for example, Sanders et al, J. Am. Chem. Soc. 2011 , 133, 949-957 (Scheme 2). Compounds of the formula S2-3 can be prepared from compounds of the formula S2-2 by reaction with a chlorinating reagent (e.g. N-chlorosuccinimide, NaOCI, t-butylhypochlorite) as described by, for example, Sanders et al, J. Am. Chem. Soc. 201 1 , 133, 949-957. Compounds of the formula S2-4 can be prepared from compounds of the formula S2-3 by reaction with an amine nucleophile (ArNHR2) as described by, for example, Altug et al, Tetrahedron Lett. 2009, 50, 7392-7394. Compounds of the formula S2-5 can be prepared from compounds of the formula S2-4 by reaction with an electrophile (e.g. methyl iodide, cyanogen bromide, acetyl chloride etc.) in the presence of a base (e.g. NaOH, pyridine, triethylamine, K2CO3, NaH) as described by, for example, Lui et al, Pest. Manag. Sci. 2009, 65, 229-234.

Scheme 2


S2-4 S2-5

Compounds of the formula S3-2 (R = Me, Et) can be prepared from compounds of the formula S3-1 by reaction with, for example, hydrochloric acid in methanol as described by, for example, Laurent et al, Molecules, 2010, 15, 4283-4293 (Scheme 3). Compounds of the formula S3-3 can be prepared from compounds of the formula S3-2 by reaction with an amine nucleophile (ArNHR2) as described by, for example, Arnold et al, WO 2008/124849. Scheme 3


Compounds of the formula S4-2 can be prepared via compounds of the formula S4-1 by reaction of compounds of the formula S1-2 with a chlorinating agent (e.g. N-chlorosuccinimide, NaOCI, t-butylhypochlorite) followed by a hydrazine [H2NN(R3)2] as described by, for example, Crimmin et al, Dalton Trans., 201 1 , 42, 514-522 (Scheme 4). Compounds of the formula S4-2 can also be prepared from compounds of the formula S1-3 by reaction with, for example, a hydrazine [H2NN(R3)2] as described by, for example, Burlison et al, WO 2009/158026.

Scheme 4

S4-1 S4-2

Compounds of the formula S5-3 can be prepared by reaction of compounds of the formula S5-1 with a reducing agent, for example, LiAIhU. The resultant compounds of the formula S5-2 can then by reacted with aryl alcohol (ArOH) under Mitsonobu conditions to form compounds of the formula S5-3 (Scheme 5). Compounds for the formula S5-5 can be prepared by reaction of compounds of the formula S5-2 with a chlorinating reagent (e.g. SOC , POCI3) as described by, for example, Miyahara et al, WO 2017/209155. The resultant compounds of the formula S5-4 can then be converted into compounds of the formula S5-2 by reaction with an arylthiol (ArSH). Compounds of the formula of the formula S5-6 can, in turn, be prepared by reaction of compounds of the formula S5-5 with an oxidizing agent (e.g. MCPBA). Compounds of the formula S1-4 can also be prepared by reducing compounds of the formula of the formula S5-1 with, e.g. DIBAL. The resultant compounds of the formula S2-1 can then be reacted with an amine (ArNHR2) in a reductive amination with, e.g.

Na(CN)BH3 to form compounds of the formula S1 -4.

Scheme 5

Compounds of the formula S6-4 can be prepared by treating compounds of the formula S6-1 a halogenating agent (e.g. POC , PBr3) (Scheme 6). The resultant compounds of the formula S6-2 can then be reacted with an amine (R2NH2) in an SNAr reaction or palladium-catalyzed amination as described by, for example, Ojida et al, WO 2018/084321 or

Hatakeyama et al, WO 2018/110497, respectively. Alternatively The resultant compounds of the formula S6-2 can be acylated with an aryl acid (or chloride) to form compounds of the formula S6-3.

Scheme 6

Compounds of the formula S7-1 , S7-2, S7-3 and S7-4 are isomers of compounds depicted in Scheme 1 - 4 and, as such, can be synthesized using analogous procedures are those described above (Scheme 7).

Scheme 7


Compounds of the formula S8-1 can be prepared in analogy to compounds of the formula S6-3 (Scheme 8). Compounds of the formula S8-2 can be prepared from compounds of the formula S6-1 by reaction with an alcohol [ArC(R9)(R10)OH] in an SNAr reaction or copper-catalyzed ether formation reaction as described by, for example, Long et al, WO

2018/059534 or Gao et al WO 2016/150193, respectively. Compounds of the formula S8-3 can be prepared from compounds of the formula S6-1 by reaction with a thiol

[ArC(R9)(R10)SH] in an SNAr reaction or palladium-catalyzed thioether formation reaction as described by, for example, Wang et al, WO 2017/198196 or Barrow et al, WO 2016/123577.

Scheme 8


Compounds of the formula S9-3 can be prepared by oxidation of compounds of the formula S9-1 with, e.g. MCPBA as described by, for example, Rinderspacher et al, US 2017/0210759

(Scheme 9). The resultant compounds of the formula S9-2 can be converted into compounds of the formula S9-3 by reaction with an acylating agent (e.g. AC2O) followed by a basic hydrolysis (e.g. with NaOH).

Scheme 9


Compounds of the formula S10-2 can be prepared by condensation of compounds of the formula S10-1 with, e.g. formamide as described by, for example, Ojida et al, WO

2018/084321 (Scheme 10).

Scheme 10

Compounds of the formula S11-2 can be prepared by reaction of compounds of the formula S1 1-1 with hydrazine as described by, for example, Siu et al, WO 2016/164285 (Scheme 1 1 ).


Compounds of the formula S12-2 (R = Me, Et) can be prepared in a palladium-catalyzed carbonylation of compounds of the formula S12-1 using CO (g) and MeOH or EtOH as described by, for example, Evans et al, WO 2017/214269 (Scheme 12). Compounds of the formula S12-4 can, in turn, be prepared from Compounds of the formula S12-2 by, e.g. basic hydrolysis compounds of the formula S12-3 can also be prepared from compounds of the formula S12-2 by reduction with, e.g. DIBAL.

Scheme 12


Compounds of the formula S12-4, S12-3 and S13-1 can be converted in known syntheses into compounds on the formula (I) as described by, for example, Crouse et al, WO

2009/102736, Crouse et al, WO 2010/093764, Crouse et al, US 2012/0202687, Crouse et al, WO 2013/009791 , Baum et al , WO 2013/1 16052, Fischer et al, WO 2013/116053, Crouse et al, WO 2014/01 1429, Jeanguenat et al, WO 2016/1 16445 and Narine et al,

WO 2018/177781 (Scheme 13).

Scheme 13


Individual compounds of formula I can also be prepared by derivatisation of other compounds of formula I or the intermediates thereof.

If the synthesis yields mixtures of isomers, a separation is generally not necessarily required since in some cases the individual isomers can be interconverted during work-up for use or during application (for example under the action of light, acids or bases). Such conversions may also take place after use, for example in the treatment of plants in the treated plant, or in the harmful fungus to be controlled.

A skilled person will readily understand that the preferences for the substituents, also in particular the ones given in the tables below for the respective substituents, given herein in connection with compounds I apply for the intermediates accordingly. Thereby, the substituents in each case have independently of each other or more preferably in

combination the meanings as defined herein.

Unless otherwise indicated, the term“compound(s) according to the invention” or “compound(s) of the invention” or“compound(s) of formula (I)”, refers to the compounds of formula I.

The term“compound(s) according to the invention”, or“compounds of formula I” comprises the compound(s) as defined herein as well as a stereoisomer, salt, tautomer or N-oxide thereof. The term“compound(s) of the present invention” is to be understood as equivalent to the term“compound(s) according to the invention”, therefore also comprising a stereoisomer, salt, tautomer or N-oxide thereof.

The term "composition(s) according to the invention" or "composition(s) of the present invention" encompasses composition(s) comprising at least one compound of formula I according to the invention as defined above. The compositions of the invention are preferably agricultural or veterinary compositions.

Depending on the substitution pattern, the compounds according to the invention may have one or more centers of chirality, in which case they are present as mixtures of enantiomers or diastereomers. The invention provides both the single pure enantiomers or pure diastereomers of the compounds according to the invention, and their mixtures and the use according to the invention of the pure enantiomers or pure diastereomers of the compounds according to the invention or their mixtures. Suitable compounds according to the invention also include all possible geometrical stereoisomers (cis/trans isomers) and mixtures thereof. Cis/trans isomers may be present with respect to an alkene, carbon-nitrogen double-bond or amide group. The term "stereoisomer(s)" encompasses both optical isomers, such as enantiomers or diastereomers, the latter existing due to more than one center of chirality in the molecule, as well as geometrical isomers (cis/trans isomers). The present invention relates to every possible stereoisomer of the compounds of formula I, i.e. to single enantiomers or diastereomers, as well as to mixtures thereof.

The compounds according to the invention may be amorphous or may exist in one or more different crystalline states (polymorphs) which may have different macroscopic properties such as stability or show different biological properties such as activities. The present invention relates to amorphous and crystalline compounds according to the invention, mixtures of different crystalline states of the respective compounds according to the invention, as well as amorphous or crystalline salts thereof.

The term "tautomers" encompasses isomers, which are derived from the compounds of formula I by the shift of an H-atom involving at least one H-atom located at a nitrogen, oxygen or sulphur atom. Examples of tautomeric forms are keto-enol forms, imine-enamine forms, urea-isourea forms, thiourea-isothiourea forms, (thio)amide-(thio)imidate forms etc.

The term "stereoisomers" encompasses both optical isomers, such as enantiomers or diastereomers, the latter existing due to more than one center of chirality in the molecule, as well as geometrical isomers (cis/trans isomers).

Depending on the substitution pattern, the compounds of the formula I may have one or more centers of chirality, in which case they are present as mixtures of enantiomers or diastereomers. One center of chirality is the carbon ring atom of the isothiazoline ring carrying radical R1. The invention provides both the pure enantiomers or diastereomers and their mixtures and the use according to the invention of the pure enantiomers or

diastereomers of the compound I or its mixtures. Suitable compounds of the formula I also include all possible geometrical stereoisomers (cis/trans isomers) and mixtures thereof.

The term N-oxides relates to a form of compounds I in which at least one nitrogen atom is present in oxidized form (as NO). To be more precise, it relates to any compound of the present invention which has at least one tertiary nitrogen atom that is oxidized to an N-oxide moiety. N-oxides of compounds I can in particular be prepared by oxidizing e.g. the ring nitrogen atom of an N-heterocycle, e.g. a pyridine or pyrimidine ring present in Ar or R11, or an imino-nitrogen present in central tricyclic core, with a suitable oxidizing agent, such as peroxo carboxylic acids or other peroxides. The person skilled in the art knows if and in which positions compounds of the present invention may form N-oxides.

Salts of the compounds of the formula I are preferably agriculturally and veterinarily acceptable salts. They can be formed in a customary method, e.g. by reacting the compound with an acid of the anion in question if the compound of formula I has a basic functionality or by reacting an acidic compound of formula I with a suitable base.

Suitable agriculturally or veterinarily acceptable salts are especially the salts of those cations or the acid addition salts of those acids whose cations and anions, which are known and accepted in the art for the formation of salts for agricultural or veterinary use

respectively, and do not have any adverse effect on the action of the compounds according to the present invention. Suitable cations are in particular the ions of the alkali metals, preferably lithium, sodium and potassium, of the alkaline earth metals, preferably calcium, magnesium and barium, and of the transition metals, preferably manganese, copper, zinc and iron, and also ammonium (NH4+) and substituted ammonium in which one to four of the hydrogen atoms are replaced by Ci-C4-alkyl, Ci-C4-hydroxyalkyl, Ci-C4-alkoxy, Ci-C4-alkoxy-Ci-C4-alkyl, hydroxy-Ci-C4-alkoxy-Ci-C4-alkyl, phenyl or -Chh-phenyl. Examples of substituted ammonium ions comprise methylammonium, isopropylammonium,

dimethylammonium, diisopropylammonium, trimethylammonium, tetramethylammonium, tetraethylammonium, tetrabutylammonium, 2-hydroxyethylammonium, 2-(2-hydroxy-ethoxy)ethylammonium, bis(2-hydroxyethyl)ammonium, benzyltrimethylammonium and benzyl-triethylammonium, furthermore phosphonium ions, sulfonium ions, preferably tri(Ci-C4-alkyl)sulfonium, and sulfoxonium ions, preferably tri(Ci-C4-alkyl)sulfoxonium.

Suitable acid addition veterinarily acceptable salts, e.g. formed by compounds of formula I containing a basic nitrogen atom, e.g. an amino group, include salts with inorganic acids, for example hydrochlorides, sulphates, phosphates, and nitrates and salts of organic acids for example acetic acid, maleic acid, dimaleic acid, fumaric acid, difumaric acid, methane sulfenic acid, methane sulfonic acid, and succinic acid.

Anions of useful acid addition salts are primarily chloride, bromide, fluoride, hydrogen sulfate, sulfate, dihydrogen phosphate, hydrogen phosphate, phosphate, nitrate, hydrogen carbonate, carbonate, hexafluorosilicate, hexafluorophosphate, benzoate, and the anions of Ci-C4-alkanoic acids, preferably formate, acetate, propionate and butyrate. They can be formed by reacting a compound of formulae I with an acid of the corresponding anion, preferably of hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid or nitric acid.

The term "invertebrate pest" as used herein encompasses animal populations, such as insects, arachnids and nematodes, which may attack plants, thereby causing substantial damage to the plants attacked, as well as ectoparasites which may infest animals, in particular warm blooded animals such as e.g. mammals or birds, or other higher animals such as reptiles, amphibians or fish, thereby causing substantial damage to the animals infested.

The term "plant propagation material" is to be understood to denote all the generative parts of the plant such as seeds and vegetative plant material such as cuttings and tubers (e. g. potatoes), which can be used for the multiplication of the plant. This includes seeds, roots, fruits, tubers, bulbs, rhizomes, shoots, sprouts and other parts of plants, including seedlings and young plants, which are to be transplanted after germination or after emergence from soil. The plant propagation materials may be treated prophylactically with a plant protection compound either at or before planting or transplanting. Said young plants may also be protected before transplantation by a total or partial treatment by immersion or pouring.

The term "plants" comprises any types of plants including "modified plants" and in particular "cultivated plants".

The term "modified plants" refers to any wild type species or related species or related genera of a cultivated plant.

The term "cultivated plants" is to be understood as including plants which have been modified by breeding, mutagenesis or genetic engineering including but not limiting to agricultural biotech products on the market or in development (cf.

http://www.bio.org/speeches/pubs/er/agri_products.asp). Genetically modified plants are plants, which genetic material has been so modified by the use of recombinant DNA techniques that under natural circumstances cannot readily be obtained by cross breeding, mutations or natural recombination. Typically, one or more genes have been integrated into the genetic material of a genetically modified plant in order to improve certain properties of the plant. Such genetic modifications also include but are not limited to targeted post-translational modification of protein(s), oligo- or polypeptides e. g. by glycosylation or polymer additions such as prenylated, acetylated or farnesylated moieties or PEG moieties.

Plants that have been modified by breeding, mutagenesis or genetic engineering, e. g. have been rendered tolerant to applications of specific classes of herbicides, such as auxin herbicides such as dicamba or 2,4-D; bleacher herbicides such as hydroxylphenylpyruvate dioxygenase (HPPD) inhibitors or phytoene desaturase (PDS) inhibittors; acetolactate synthase (ALS) inhibitors such as sulfonyl ureas or imidazolinones; enolpyruvylshikimate-3-phosphate synthase (EPSPS) inhibitors, such as glyphosate; glutamine synthetase (GS) inhibitors such as glufosinate; protoporphyrinogen-IX oxidase inhibitors; lipid biosynthesis inhibitors such as acetyl CoA carboxylase (ACCase) inhibitors; or oxynil (i. e. bromoxynil or ioxynil) herbicides as a result of conventional methods of breeding or genetic engineering. Furthermore, plants have been made resistant to multiple classes of herbicides through multiple genetic modifications, such as resistance to both glyphosate and glufosinate or to both glyphosate and a herbicide from another class such as ALS inhibitors, HPPD inhibitors, auxin herbicides, or ACCase inhibitors. These herbicide resistance technologies are e. g. described in Pest Managem. Sci. 61 , 2005, 246; 61 , 2005, 258; 61 , 2005, 277; 61 , 2005, 269; 61 , 2005, 286; 64, 2008, 326; 64, 2008, 332; Weed Sci. 57, 2009, 108; Austral. J.

Agricult. Res. 58, 2007, 708; Science 316, 2007, 1 185; and references quoted therein.

Several cultivated plants have been rendered tolerant to herbicides by conventional methods of breeding (mutagenesis), e. g. Clearfield® summer rape (Canola, BASF SE, Germany) being tolerant to imidazolinones, e. g. imazamox, or ExpressSun® sunflowers (DuPont, USA) being tolerant to sulfonyl ureas, e. g. tribenuron. Genetic engineering methods have been used to render cultivated plants such as soybean, cotton, corn, beets and rape, tolerant to herbicides such as glyphosate and glufosinate, some of which are commercially available under the trade names RoundupReady® (glyphosate-tolerant, Monsanto, U.S.A.),

Cultivance® (imidazolinone tolerant, BASF SE, Germany) and LibertyLink® (glufosinate-tolerant, Bayer CropScience, Germany).

Furthermore, plants are also covered that are by the use of recombinant DNA techniques capable to synthesize one or more insecticidal proteins, especially those known from the bacterial genus Bacillus, particularly from Bacillus thuringiensis, such as d-endotoxins, e. g. CrylA(b), CrylA(c), CrylF, CrylF(a2), CryllA(b), CrylllA, Cryl 11 B(b1 ) or Cry9c; vegetative insecticidal proteins (VIP), e. g. VIP1 , VIP2, VIP3 or VIP3A; insecticidal proteins of bacteria colonizing nematodes, e. g. Photorhabdus spp. or Xenorhabdus spp.; toxins produced by animals, such as scorpion toxins, arachnid toxins, wasp toxins, or other insect-specific neurotoxins; toxins produced by fungi, such Streptomycetes toxins, plant lectins, such as pea or barley lectins; agglutinins; proteinase inhibitors, such as trypsin inhibitors, serine protease inhibitors, patatin, cystatin or papain inhibitors; ribosome-inactivating proteins (RIP), such as ricin, maize-RIP, abrin, luffin, saporin or bryodin; steroid metabolism enzymes, such as 3-hydroxysteroid oxidase, ecdysteroid-IDP-glycosyl-transferase, cholesterol oxidases, ecdysone inhibitors or HMG-CoA-reductase; ion channel blockers, such as blockers of sodium or calcium channels; juvenile hormone esterase; diuretic hormone receptors

(helicokinin receptors); stilben synthase, bibenzyl synthase, chitinases or glucanases. In the context of the present invention these insecticidal proteins or toxins are to be understood expressly also as pre-toxins, hybrid proteins, truncated or otherwise modified proteins.

Hybrid proteins are characterized by a new combination of protein domains, (see, e. g.

WO 02/015701 ). Further examples of such toxins or genetically modified plants capable of synthesizing such toxins are disclosed, e. g., in EP-A 374 753, WO 93/007278,

WO 95/34656, EP-A 427 529, EP-A 451 878, WO 03/18810 und WO 03/52073. The methods for producing such genetically modified plants are generally known to the person skilled in the art and are described, e. g. in the publications mentioned above. These insecticidal proteins contained in the genetically modified plants impart to the plants producing these proteins tolerance to harmful pests from all taxonomic groups of athropods, especially to beetles (Coeloptera), two-winged insects (Diptera), and moths (Lepidoptera)

and to nematodes (Nematoda). Genetically modified plants capable to synthesize one or more insecticidal proteins are, e. g., described in the publications mentioned above, and some of which are commercially available such as YieldGard® (corn cultivars producing the CrylAb toxin), YieldGard® Plus (corn cultivars producing CrylAb and Cry3Bb1 toxins), Starlink® (corn cultivars producing the Cry9c toxin), Herculex® RW (corn cultivars producing Cry34Ab1 , Cry35Ab1 and the enzyme Phosphinothricin-N-Acetyltransferase [PAT]);

NuCOTN® 33B (cotton cultivars producing the Cry1 Ac toxin), Bollgard® I (cotton cultivars producing the CrylAc toxin), Bollgard® II (cotton cultivars producing CrylAc and Cry2Ab2 toxins); VIPCOT® (cotton cultivars producing a VIP-toxin); NewLeaf® (potato cultivars producing the Cry3A toxin); Bt-Xtra®, NatureGard®, KnockOut®, BiteGard®, Protecta®, Bt1 1 (e. g. Agrisure® CB) and Bt176 from Syngenta Seeds SAS, France, (corn cultivars producing the CrylAb toxin and PAT enyzme), MIR604 from Syngenta Seeds SAS, France (corn cultivars producing a modified version of the Cry3A toxin, c.f. WO 03/018810), MON 863 from Monsanto Europe S.A., Belgium (corn cultivars producing the Cry3Bb1 toxin), IPC 531 from Monsanto Europe S.A., Belgium (cotton cultivars producing a modified version of the CrylAc toxin) and 1507 from Pioneer Overseas Corporation, Belgium (corn cultivars producing the Cry1 F toxin and PAT enzyme).

Furthermore, plants are also covered that are by the use of recombinant DNA techniques capable to synthesize one or more proteins to increase the resistance or tolerance of those plants to bacterial, viral or fungal pathogens. Examples of such proteins are the so-called “pathogenesis-related proteins” (PR proteins, see, e. g. EP-A 392 225), plant disease resistance genes (e. g. potato cultivars, which express resistance genes acting against Phytophthora infestans derived from the mexican wild potato Solanum bulbocastanum) or T4-lysozym (e. g. potato cultivars capable of synthesizing these proteins with increased resistance against bacteria such as Erwinia amylvora). The methods for producing such genetically modified plants are generally known to the person skilled in the art and are described, e. g. in the publications mentioned above.

Furthermore, plants are also covered that are by the use of recombinant DNA techniques capable to synthesize one or more proteins to increase the productivity (e. g. bio mass production, grain yield, starch content, oil content or protein content), tolerance to drought, salinity or other growth-limiting environmental factors or tolerance to pests and fungal, bacterial or viral pathogens of those plants.

Furthermore, plants are also covered that contain by the use of recombinant DNA techniques a modified amount of substances of content or new substances of content, specifically to improve human or animal nutrition, e. g. oil crops that produce health-promoting long-chain omega-3 fatty acids or unsaturated omega-9 fatty acids (e. g. Nexera® rape, DOW Agro Sciences, Canada).

Furthermore, plants are also covered that contain by the use of recombinant DNA techniques a modified amount of substances of content or new substances of content, specifically to improve raw material production, e. g. potatoes that produce increased amounts of amylopectin (e. g. Amflora® potato, BASF SE, Germany).

The organic moieties mentioned in the above definitions of the variables are - like the term halogen - collective terms for individual listings of the individual members. The prefix Cn-Cm indicates in each case the possible number of carbon atoms in the group.

The term halogen denotes in each case F, Br, Cl or I, in particular F, Cl or Br.

The term "alkyl" as used herein and in the alkyl moieties of alkoxy, alkylthio, and the like refers to saturated straight-chain or branched hydrocarbon radicals having 1 to 2 ("C1-C2-alkyl"), 1 to 3 ("Ci-C3-alkyl"),1 to 4 ("Ci-C4-alkyl") or 1 to 6 ("Ci-C6-alkyl") carbon atoms. Ci-C2-Alkyl is CFh or C2H5. Ci-C3-Alkyl is additionally propyl and isopropyl. Ci-C4-Alkyl is additionally butyl, 1-methylpropyl (sec-butyl), 2-methylpropyl (isobutyl) or 1 , 1 -dimethylethyl (tert-butyl). Ci-C6-Alkyl is additionally also, for example, pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 2,2-dimethylpropyl, 1-ethylpropyl, 1 ,1-dimethylpropyl, 1 ,2-dimethylpropyl, hexyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1 ,1-dimethylbutyl, 1 ,2-dimethylbutyl, 1 ,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl, 2-ethylbutyl, 1 ,1 ,2-trimethylpropyl, 1 ,2,2-trimethylpropyl, 1 -ethyl-1 -methylpropyl, or 1 -ethyl-2-methylpropyl.

The term "haloalkyl" as used herein, which is also expressed as "alkyl which is partially or fully halogenated", refers to straight-chain or branched alkyl groups having 1 to 2 ("C1-C2-haloalkyl"), 1 to 3 ("Ci-C3-haloalkyl"), 1 to 4 ("Ci-C4-haloalkyl") or 1 to 6 ("Ci-C6-haloalkyl") carbon atoms (as mentioned above), where some or all of the hydrogen atoms in these groups are replaced by halogen atoms as mentioned above: in particular Ci-C2-haloalkyl, such as chloromethyl, bromomethyl, dichloromethyl, trichloromethyl, fluoromethyl, difluoromethyl, trifluoromethyl, chlorofluoromethyl, dichlorofluoromethyl, chlorodifluoromethyl,

1-chloroethyl, 1-bromoethyl, 1-fluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl,

2-chloro-2-fluoroethyl, 2-chloro-2,2-difluoroethyl, 2,2-dichloro-2-fluoroethyl, 2,2,2-trichloroethyl or pentafluoroethyl. Ci-C3-haloalkyl is additionally, for example, 1-fluoropropyl, 2-fluoropropyl, 3-fluoropropyl, 1 ,1 -difluoropropyl, 2,2-difluoropropyl, 1 ,2-difluoropropyl, 3,3-difluoropropyl, 3,3,3-trifluoropropyl, heptafluoropropyl, 1 ,1 ,1 -trifluoroprop-2-yl, 3-chloropropyl and the like. Examples for Ci-C4-haloalkyl are, apart those mentioned for Ci-C3-haloalkyl, 4-chlorobutyl and the like.

The term "alkylene" (or alkanediyl) as used herein in each case denotes an alkyl radical as defined above, wherein one hydrogen atom at any position of the carbon backbone is replaced by one further binding site, thus forming a bivalent moiety. Alkylene has preferably 1 to 6 carbon atoms (Ci-C6-alkylene), 2 to 6 carbon atoms (C2-C6-alkylene), in particular 1 to

4 carbon atoms (Ci-C4-alkylene) or 2 to 4 carbon atoms (C2-C4-alkylene). Examples of alkylene are methylene (CH2), 1 , 1 -ethandiyl, 1 ,2-ethandiyl, 1 ,3-propandiyl, 1 ,2-propandiyl,

2.2-propandiyl, 1 ,4-butandiyl, 1 ,2-butandiyl, 1 ,3-butandiyl, 2,3-butandiyl, 2,2-butandiyl, 1 ,5-pentandiyl, 2,2-dimethylpropan-1 ,3-diyl, 1 ,3-dimethyl-1 ,3-propandiyl, 1 ,6-hexandiyl etc.

The term "alkenyl" as used herein refers to monounsaturated straight-chain or branched hydrocarbon radicals having 2 to 3 ("C2-C3-alkenyl"), 2 to 4 ("C2-C4-alkenyl") or 2 to 6 ("C2-C6-alkenyl) carbon atoms and a double bond in any position, for example C2-C3-alkenyl, such as ethenyl, 1-propenyl, 2-propenyl or 1-methylethenyl; C2-C4-alkenyl, such as ethenyl, 1-propenyl, 2-propenyl, 1-methylethenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1 -methyl-1 -propenyl, 2-methyl-1-propenyl, 1-methyl-2-propenyl or 2-methyl-2-propenyl; C2-C6-alkenyl, such as ethenyl, 1-propenyl, 2-propenyl, 1-methylethenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1 -methyl-1 -propenyl, 2-methyl-1 -propenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 1 -methyl-1 -butenyl, 2-methyl-1-butenyl, 3-methyl-1-butenyl,

1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, 1-methyl-3-butenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl, 1 ,1-dimethyl-2-propenyl, 1 ,2-dimethyl-1 -propenyl, 1 ,2-dimethyl- 2-propenyl, 1 -ethyl-1 -propenyl, 1-ethyl-2-propenyl, 1-hexenyl, 2-hexenyl, 3-hexenyl,

4-hexenyl, 5-hexenyl, 1 -methyl-1 -pentenyl, 2-methyl-1-pentenyl, 3-methyl-1-pentenyl, 4-methyl-1-pentenyl, 1-methyl-2-pentenyl, 2-methyl-2-pentenyl, 3-methyl-2-pentenyl, 4-methyl-2-pentenyl, 1-methyl-3-pentenyl, 2-methyl-3-pentenyl, 3-methyl-3-pentenyl, 4-methyl-3-pentenyl, 1-methyl-4-pentenyl, 2-methyl-4-pentenyl, 3-methyl-4-pentenyl, 4-methyl-4-pentenyl, 1 ,1-dimethyl-2-butenyl, 1 ,1-dimethyl-3-butenyl, 1 ,2-dimethyl-1 -butenyl,

1.2-dimethyl-2-butenyl, 1 ,2-dimethyl-3-butenyl, 1 ,3-dimethyl-1 -butenyl, 1 ,3-dimethyl-2-butenyl, 1 ,3-dimethyl-3-butenyl, 2,2-dimethyl-3-butenyl, 2, 3-dimethyl-1 -butenyl, 2,3-dimethyl-2-butenyl, 2,3-dimethyl-3-butenyl, 3, 3-dimethyl-1 -butenyl, 3,3-dimethyl-2-butenyl,

1 -ethyl-1 -butenyl, 1-ethyl-2-butenyl, 1-ethyl-3-butenyl, 2 -ethyl-1 -butenyl, 2-ethyl-2-butenyl, 2-ethyl-3-butenyl, 1 ,1 ,2-trimethyl-2-propenyl, 1 -ethyl-1 -methyl-2-propenyl, 1-ethyl-2-methyl-1-propenyl, 1-ethyl-2-methyl-2-propenyl and the like.

The term "alkynyl" as used herein refers to straight-chain or branched hydrocarbon groups having 2 to 3 ("C2-C3-alkynyl"), 2 to 4 ("C2-C4-alkynyl") or 2 to 6 ("C2-C6-alkynyl") carbon atoms and one or two triple bonds in any position, for example C2-C3-alkynyl, such as ethynyl, 1-propynyl or 2-propynyl; C2-C4-alkynyl, such as ethynyl, 1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl, 3-butynyl, 1-methyl-2-propynyl and the like, C2-C6-alkynyl, such as ethynyl, 1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl, 3-butynyl, 1-methyl-2-propynyl, 1-pentynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl, 1-methyl-2-butynyl, 1-methyl-3-butynyl, 2-methyl-3-butynyl, 3-methyl-1-butynyl, 1 ,1-dimethyl-2-propynyl, 1-ethyl-2-propynyl, 1-hexynyl,

2-hexynyl, 3-hexynyl, 4-hexynyl, 5-hexynyl, 1-methyl-2-pentynyl, 1-methyl-3-pentynyl, 1-methyl-4-pentynyl, 2-methyl-3-pentynyl, 2-methyl-4-pentynyl, 3-methyl-1-pentynyl, 3-methyl-

4-pentynyl, 4-methyl-1-pentynyl, 4-methyl-2-pentynyl, 1 ,1-dimethyl-2-butynyl, 1 , 1 -dimethyl-3-butynyl, 1 ,2-dimethyl-3-butynyl, 2,2-dimethyl-3-butynyl, 3,3-dimethyl-1-butynyl, 1 -ethyl-2-butynyl, 1 -ethyl-3-butynyl, 2-ethyl-3-butynyl, 1 -ethyl-1 -methyl-2-propynyl and the like;

The term "cycloalkyl" as used herein refers to mono- or bi- or polycyclic saturated hydrocarbon radicals having in particular 3 to 6 ("C3-C6-cycloalkyl") or 3 to 5 ("C3-C5-cycloalkyl") or 3 to 4 ("C3-C4-cycloalkyl") carbon atoms. Examples of monocyclic radicals having 3 to 4 carbon atoms comprise cyclopropyl and cyclobutyl. Examples of monocyclic radicals having 3 to 5 carbon atoms comprise cyclopropyl, cyclobutyl and cyclopentyl.

Examples of monocyclic radicals having 3 to 6 carbon atoms comprise cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl. Examples of monocyclic radicals having 3 to 8 carbon atoms comprise cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and cyclooctyl. Examples of bicyclic radicals having 7 or 8 carbon atoms comprise bicyclo[2.2.1]heptyl, bicyclo[3.1.1]heptyl, bicyclo[2.2.2]octyl and bicyclo[3.2.1]octyl. Preferably, the term cycloalkyl denotes a monocyclic saturated hydrocarbon radical.

The term "cycloalkoxy" as used herein refers to a cycloalkyl radical, in particular a monocyclic cycloalkyl radical, as defined above having in particular 3 to 6 ("C3-C6-cycloalkoxy") or 3 to 5 ("Cs-Cs-cycloalkoxy") or 3 to 4 ("C3-C4-cycloalksoxy") carbon atoms, which is bound via an oxygen atom to the remainder of the molecule.

The term "cycloalkyl-Ci-C4-alkyl" refers to a Cs-Cs-cycloalkyl ("C3-C8-cycloalkyl-Ci-C4-alkyl"), preferably a C3-C6-cycloalkyl ("C3-C6-cycloalkyl-Ci-C4-alkyl"), more preferably a C3-C4-cycloalkyl ("C3-C4-cycloalkyl-Ci-C4-alkyl") as defined above (preferably a monocyclic cycloalkyl group) which is bound to the remainder of the molecule via a Ci-C4-alkyl group, as defined above. Examples for C3-C4-cycloalkyl-Ci-C4-alkyl are cyclopropylmethyl,

cyclopropylethyl, cyclopropylpropyl, cyclobutylmethyl, cyclobutylethyl and cyclobutylpropyl, Examples for C3-C6-cycloalkyl-Ci-C4-alkyl, apart those mentioned for C3-C4-cycloalkyl-Ci-C4-alkyl, are cyclopentylmethyl, cyclopentylethyl, cyclopentyl propyl, cyclohexylmethyl, cyclohexylethyl and cyclohexylpropyl.

The term "Ci-C2-alkoxy" is a Ci-C2-alkyl group, as defined above, attached via an oxygen atom. The term "Ci-C3-alkoxy" is a Ci-C3-alkyl group, as defined above, attached via an oxygen atom. The term "Ci-C4-alkoxy" is a Ci-C4-alkyl group, as defined above, attached via an oxygen atom. The term "Ci-C6-alkoxy" is a Ci-C6-alkyl group, as defined above, attached via an oxygen atom. The term "Ci-Cio-alkoxy" is a Ci-Cio-alkyl group, as defined above, attached via an oxygen atom. Ci-C2-Alkoxy is OCH3 or OC2H5. Ci-C3-Alkoxy is additionally, for example, n-propoxy and 1-methylethoxy (isopropoxy). Ci-C4-Alkoxy is additionally, for example, butoxy, 1-methylpropoxy (sec-butoxy), 2-methylpropoxy (isobutoxy) or 1 ,1-dimethylethoxy (tert-butoxy). Ci-C6-Alkoxy is additionally, for example, pentoxy, 1-methylbutoxy, 2-methylbutoxy, 3-methylbutoxy, 1 ,1-dimethylpropoxy, 1 ,2-dimethylpropoxy,

2.2-dimethylpropoxy, 1-ethylpropoxy, hexoxy, 1-methylpentoxy, 2-methylpentoxy,

3-methylpentoxy, 4-methylpentoxy, 1 ,1-dimethylbutoxy, 1 ,2-dimethylbutoxy,

1.3-dimethylbutoxy, 2,2-dimethylbutoxy, 2,3-dimethylbutoxy, 3,3-dimethylbutoxy,

1-ethylbutoxy, 2-ethylbutoxy, 1 ,1 ,2-trimethylpropoxy, 1 ,2,2-trimethylpropoxy, 1 -ethyl-1 -methylpropoxy or 1-ethyl-2-methylpropoxy. C-i-Cs-Alkoxy is additionally, for example, heptyloxy, octyloxy, 2-ethylhexyloxy and positional isomers thereof. C-i-C-io-Alkoxy is additionally, for example, nonyloxy, decyloxy and positional isomers thereof.

The term "Ci-C2-haloalkoxy" is a Ci-C2-haloalkyl group, as defined above, attached via an oxygen atom. The term "Ci-C3-haloalkoxy" is a Ci-C3-haloalkyl group, as defined above, attached via an oxygen atom. The term "Ci-C4-haloalkoxy" is a Ci-C4-haloalkyl group, as defined above, attached via an oxygen atom. The term "Ci-C6-haloalkoxy" is a C1-C6-haloalkyl group, as defined above, attached via an oxygen atom. Ci-C2-Haloalkoxy is, for example, OCH2F, OCHF2, OCF3, OCH2CI, OCHC , OCCI3, chlorofluoromethoxy,

dichlorofluoromethoxy, chlorodifluoromethoxy, 2-fluoroethoxy, 2-chloroethoxy,

2-bromoethoxy, 2-iodoethoxy, 2,2-difluoroethoxy, 2,2,2-trifluoroethoxy, 2-chloro-2-fluoroethoxy, 2-chloro-2,2-difluoroethoxy, 2,2-dichloro-2-fluoroethoxy, 2,2,2-trichloroethoxy or OC2F5. Ci-C3-Haloalkoxy is additionally, for example, 2-fluoropropoxy, 3-fluoropropoxy, 2,2-difluoropropoxy, 2,3-difluoropropoxy, 2-chloropropoxy, 3-chloropropoxy, 2,3-dichloropropoxy,

2-bromopropoxy, 3-bromopropoxy, 3,3,3-trifluoropropoxy, 3,3,3-trichloropropoxy, OCH2-C2F5, OCF2-C2F5, 1-(CH2F)-2-fluoroethoxy, 1-(CH2CI)-2-chloroethoxy or 1-(CH2Br)-2-bromoethoxy. Ci-C4-Haloalkoxy is additionally, for example, 4-fluorobutoxy, 4-chlorobutoxy, 4-bromobutoxy or nonafluorobutoxy. Ci-C6-Haloalkoxy is additionally, for example, 5-fluoropentoxy, 5-chloropentoxy, 5-brompentoxy, 5-iodopentoxy, undecafluoropentoxy, 6-fluorohexoxy, 6-chlorohexoxy, 6-bromohexoxy, 6-iodohexoxy or dodecafluorohexoxy.

The term "Ci-C6-alkoxy-Ci-C4-alkyl" as used herein, refers to a straight-chain or branched alkyl having 1 to 4 carbon atoms, as defined above, where one hydrogen atom is replaced by a Ci-C6-alkoxy group, as defined above. Examples are methoxymethyl, ethoxymethyl, propoxymethyl, isopropoxymethyl, n-butoxymethyl, sec-butoxymethyl, isobutoxymethyl, tert-butoxymethyl, 1-methoxyethyl, 1-ethoxyethyl, 1-propoxyethyl, 1-isopropoxyethyl, 1-n-butoxyethyl, 1-sec-butoxyethyl, 1-isobutoxyethyl, 1-tert-butoxyethyl, 2-methoxyethyl, 2-ethoxyethyl, 2-propoxyethyl, 2-isopropoxyethyl, 2-n-butoxyethyl, 2-sec-butoxyethyl, 2-isobutoxyethyl, 2-tert-butoxyethyl, 1-methoxypropyl, 1-ethoxypropyl, 1-propoxy propyl, 1-isopropoxypropyl, 1-n-butoxypropyl, 1-sec-butoxypropyl, 1-isobutoxypropyl, 1-tert-butoxypropyl, 2-methoxypropyl, 2-ethoxypropyl, 2-propoxypropyl, 2-isopropoxypropyl, 2-n-butoxypropyl, 2-sec-butoxypropyl, 2-isobutoxypropyl, 2-tert-butoxypropyl, 3-methoxypropyl,

3-ethoxypropyl, 3-propoxypropyl, 3-isopropoxypropyl, 3-n-butoxypropyl, 3-sec-butoxypropyl, 3-isobutoxypropyl, 3-tert-butoxypropyl and the like.

The term "alkoxyalkoxy" as used herein refers to an alkoxyalkyl radical, in particular a Ci-C6-alkoxy-Ci-C4-alkyl radical, as defined above, which is bound via an oxygen atom to the remainder of the molecule. Examples thereof are OCH2-OCH3, OCH2-OC2H5, n-propoxymethoxy, OCH2-OCH(CH3)2, n-butoxymethoxy, (l-methylpropoxy)methoxy, (2-methylpropoxy)methoxy, OCH2-OC(CH3)3, 2-(methoxy)ethoxy, 2-(ethoxy)ethoxy, 2-(n-propoxy)ethoxy, 2-(1-methylethoxy)ethoxy, 2-(n-butoxy)ethoxy, 2-(1-methylpropoxy)ethoxy, 2-(2-methylpropoxy)ethoxy, 2-(1 ,1-dimethylethoxy)ethoxy, etc.

The substituent "oxo" replaces a CH2 by a C(=0) group.

The term "aryl" relates to phenyl and bi- or polycyclic carbocycles having at least one fused phenylene ring, which is bound to the remainder of the molecule. Examples of bi- or polycyclic carbocycles having at least one phenylene ring include naphthyl,

tetrahydronaphthyl, indanyl, indenyl, anthracenyl, fluorenyl etc.

The term "aryl-Ci-C4-alkyl" relates to Ci-C4-alkyl, as defined above, wherein one hydrogen atom has been replaced by an aryl radical, in particular a phenyl radical. Particular examples of aryl-Ci-C4-alkyl include -Chh-phenyl, 1-phenethyl, 2-phenetyl, 1-phenylpropyl, 2-phenylpropyl, 3-phenyl-1 -propyl and 2-phenyl-2-propyl.

The term "aryloxy-Ci-C4-alkyl" relates to Ci-C4-alkyl, as defined above, wherein one hydrogen atom has been replaced by an aryloxy radical, in particular a phenoxy radical. Particular examples of aryloxy-Ci-C4-alkyl include phenoxymethyl, 1-phenoxyethyl, 2-phenoxyetyl, 1-phenoxypropyl, 2-phenoxypropyl, 3-phenoxy-1 -propyl and 2-phenoxy-2-propyl.

The term "aryl-Ci-C4-carbonyl" relates to aryl as defined above, , in particular a phenyl radical, which is bound by a carbonyl to the remainder of the molecule. Particular examples of arylcarbonyl include benzoyl, 1-naphthoyl and 2-naphthoyl.

The term“hetaryl” relates to aromatic heterocycles having either 5 or 6 ring atoms (5- or 6-membered hetaryl) and being monocyclic or 8, 9 or 10 ring atoms and bing bicyclic. Hetaryl will generally have at least one ring atom selected from O, S and N, which in case of N may be an imino-nitrogen or an amino-nitrogen, which carries hydrogen or a radical different from hydrogen. Hetaryl may have 1 , 2, 3 or 4 further nitrogen atoms as ring members, which are imino nitrogens. Examples of 5- or 6-membered hetaryl include 2-furyl, 3-furyl, 2-thienyl, 3-thienyl, 1-pyrrolyl, 2-pyrrolyl, 3-pyrrolyl, 1-pyrazolyl, 3-pyrazolyl, 4-pyrazolyl, 5-pyrazolyl, 2-oxazolyl, 4-oxazolyl, 5-oxazolyl, 2-thiazolyl, 4-thiazolyl, 5-thiazolyl, 1-imidazolyl, 2-imidazolyl, 4-imidazolyl, 1 ,3,4-triazol-1-yl, 1 ,3,4-triazol-2-yl, 1 ,3,4-oxadiazolyl-2-yl, 1 ,3,4-thiadiazol-2-yl, 2-pyridinyl, 3-pyridinyl, 4-pyridinyl, 3-pyridazinyl, 4-pyridazinyl, 2-pyrimidinyl, 4-pyrimidinyl, 5-pyrimidinyl, 2-pyrazinyl and 1 ,3,5-triazin-2-yl.. Examples of 8-, 9- or 10-membered hetaryl include, for example, quinolinyl, isoquinolinyl, cinnolinyl, indolyl, indolizynyl, isoindolyl, indazolyl, benzofuryl, benzothienyl, benzo[b]thiazolyl, benzoxazolyl, benzthiazolyl,

benzimidazolyl, imidazo[1 ,2-a]pyridine-2-yl, thieno[3,2-b]pyridine-5-yl, imidazo-[2,1 -b]-thiazol-6-yl and 1 ,2,4-triazolo[1 ,5-a]pyridine-2-yl.

Examples of N-bound 5-, 6-, 7 or 8-membered saturated heterocycles include: pyrrolidin-1 -yl, pyrazolidin-1 -yl, imidazolidin-1 -yl, oxazolidin-3-yl, isoxazolidin-2-yl, thiazolidin-3-yl, isothiazolidin-2-yl, piperidin-1 -yl, piperazin-1 -yl, morpholin-4-yl, thiomorpholin-4-yl, 1 -oxothiomorpholin-4-yl, 1 ,1 -dioxothiomorpholin-4-yl, azepan-1 -yl and the like.

The term "hetaryl-Ci-C4-alkyl" relates to Ci-C4-alkyl, as defined above, wherein one hydrogen atom has been replaced by a hetaryl radical, in particular a pyridyl radical.

Particular examples of hetaryl-Ci-C4-alkyl include 2-pyridylmethyl, 3-pyridylmethyl, 4-pyridylmethyl, 1 -(2-pyridyl)ethyl, 2-(2-pyridyl)ethyl, 1 -(3-pyridyl)ethyl, 2-(3-pyridyl)ethyl, 1 -(4-pyridyl)ethyl, 2-(4-pyridyl)ethyl etc..

The term "hetaryloxy-Ci-C4-alkyl" relates to Ci-C4-alkyl, as defined above, wherein one hydrogen atom has been replaced by an hetaryloxy radical, in particular a pyridyloxy radical. Particular examples of hetaryloxy-Ci-C4-alkyl include 2-pyridyloxymethyl, 3-pyridyloxymethyl, 4-pyridyloxymethyl, 1 -(2-pyridyloxy)ethyl, 2-(2-pyridyloxy)ethyl, 1 -(3-pyridyloxy)ethyl, 2-(3-pyridyloxy)ethyl, 1 -(4-pyridyloxy)ethyl, 2-(4-pyridyloxy)ethyl etc.

The term "hetaryl-Ci-C4-carbonyl" relates to hetaryl as defined above, in particular a C-bound hetaryl radical, e.g. 2-, 3-or 4-pyridyl, 2- or 3-thienyl, 2- or 3-furyl, 1 -, 2- or 3-pyrrolyl,

2- or 4-pyrimidinyl, pyridazinyl, 1 -, 3- or 4-pyrazolyl, 1 -, 2- or 4-imidazolyl radical, which is bound by a carbonyl to the remainder of the molecule.

The term“substituted” if not specified otherwise refers to substituted with 1 , 2 or maximum possible number of substituents. If substituents as defined in compounds of formula I are more than one then they are independently from each other are same or different if not mentioned otherwise.

In one preferred embodiment, A1 is N, A2 is CRA2, A3 is CRA3;

In another preferred embodiment, A1 is CRA1, A2 is N, A3 is CRA3;

In another preferred embodiment, A1 is CRA1, A2 is CRA2, A3 is N;

In another preferred embodiment, A1 is N, A2 is N, A3 is CRA3;

In another preferred embodiment, A1 is N, A2 is CRA2, A3 is N;

In another preferred embodiment, A1 is CRA1, A2 is N, A3 is N;

In one preferred embodiment, B1 is CRB1, B2 is CRB2, B3 is CRB3;

In another preferred embodiment, B1 is N, B2 is CRB2, B3 is CRB3;

In another preferred embodiment, B1 is CRB1, B2 is N, B3 is CRB3;

In another preferred embodiment, B1 is N, B2 is N, B3 is CRB3;

In another preferred embodiment, B1 is N, B2 is N, B3 is N;

In another preferred embodiment, A1 is N, A2 is CRA2, A3 is CRA3, B1 is CRB1, B2 is CRB2, B3 is CRB3;

In another preferred embodiment, A1 is N, A2 is CRA2, A3 is CRA3, B1 is N, B2 is CRB2, B3 is CRB3;

In another preferred embodiment, A1 is N, A2 is CRA2, A3 is CRA3, B1 is CRB1, B2 is N, B3 is CRB3;

In another preferred embodiment, A1 is N, A2 is CRA2, A3 is CRA3, B1 is N, B2 is N, B3 is CRB3;

In another preferred embodiment, A1 is N, A2 is CRA2, A3 is CRA3, B1 is N, B2 is N, B3 is N;

In another preferred embodiment, A1 is CRA1, A2 is N, A3 is CRA3, B1 is CRB1, B2 is CRB2, B3 is CRB3;

In another preferred embodiment, A1 is CRA1, A2 is N, A3 is CRA3, B1 is N, B2 is CRB2, B3 is CRB3;

In another preferred embodiment, A1 is CRA1, A2 is N, A3 is CRA3, B1 is CRB1, B2 is N, B3 is CRB3;

In another preferred embodiment, A1 is CRA1, A2 is N, A3 is CRA3, B1 is N, B2 is N, B3 is CRB3;

In another preferred embodiment, A1 is CRA1, A2 is N, A3 is CRA3, B1 is N, B2 is N, B3 is N;

In another preferred embodiment, A1 is CRA1, A2 is CRA2, A3 is N, B1 is CRB1, B2 is CRB2, B3 is CRB3;

In another preferred embodiment, A1 is CRA1, A2 is CRA2, A3 is N, B1 is N, B2 is CRB2, B3 is CRB3;

In another preferred embodiment, A1 is CRA1, A2 is CRA2, A3 is N, B1 is CRB1, B2 is N, B3 is CRB3;

In another preferred embodiment, A1 is CRA1, A2 is CRA2, A3 is N, B1 is N, B2 is N, B3 is CRB3;

In another preferred embodiment, A1 is CRA1, A2 is CRA2, A3 is N, B1 is N, B2 is N, B3 is N;

In another preferred embodiment, A1 is N, A2 is N, A3 is CRA3, B1 is CRB1, B2 is CRB2, B3 is

CRB3;

In another preferred embodiment, A1 is N, A2 is N, A3 is CRA3, B1 is N, B2 is CRB2, B3 is CRB3;

In another preferred embodiment, A1 is N, A2 is N, A3 is CRA3, B1 is CRB1, B2 is N, B3 is CRB3;

In another preferred embodiment, A1 is N, A2 is N, A3 is CRA3, B1 is N, B2 is N, B3 is CRB3;

In another preferred embodiment, A1 is N, A2 is N, A3 is CRA3, B1 is N, B2 is N, B3 is N;

In another preferred embodiment, A1 is N, A2 is CRA2, A3 is N, B1 is CRB1, B2 is CRB2, B3 is

CRB3;

In another preferred embodiment, A1 is N, A2 is CRA2, A3 is N, B1 is N, B2 is CRB2, B3 is CRB3;

In another preferred embodiment, A1 is N, A2 is CRA2, A3 is N, B1 is CRB1, B2 is N, B3 is CRB3;

In another preferred embodiment, A1 is N, A2 is CRA2, A3 is N, B1 is N, B2 is N, B3 is CRB3;

In another preferred embodiment, A1 is N, A2 is CRA2, A3 is N, B1 is N, B2 is N, B3 is N;

In one preferred embodiment, RA1, RA2, RA3 independently of each other are selected from H, halogen, OH, CN, Ci-C6-alkyl, Ci-C6-alkoxy, tri-Ci-C6-alkylsilyl, Ci-C6-alkoxy-Ci-C4-alkyl, C3-C6-cycloalkyl, wherein the alkyl, alkoxy, cycloalkyl moieties are unsubstituted or substituted with halogen,

C(=0)-ORa, NRbRc, C(=0)-NRbRc, C(=0)-Rd, S02NRbRc, and S(=0)mRe;

In another preferred embodiment, RA1, RA2, RA3 independently of each other are selected from H, halogen, Ci-C6-alkyl, and C3-C6-cycloalkyl, wherein the alkyl or cycloalkyl moieties are unsubstituted or substituted with halogen.

In another preferred embodiment, RA1, RA2, RA3 independently of each other are selected from H, Cl, Br, F, CH3, C2H5, n-C3H7, isopropyl, cyclopropyl, CH2F, CHF2, and CF3.

In another preferred embodiment, RA1, RA2, RA3 are H.

In one preferred embodiment, RB1, RB2, RB3 independently of each other are H, halogen, or Ci-C6-alkyl;

In another preferred embodiment, RB1, RB2, RB3 independently of each other are H, Cl, Br, F, CH3, C2H5, n-C3H7, or isopropyl.

In another preferred embodiment, RB1, RB2, RB3 independently of each other are H, or CH3.

In another preferred embodiment, RB1, RB2, RB3 are H.

In one preferred embodiment, Q is -C(R4R5)-0-, wherein C is bound to Ar.

In another preferred embodiment, Q is -C(R4R5)-0-, wherein O is bound to Ar.

In another preferred embodiment, Q is -C(=0)-0-, wherein C is bound to Ar.

In another preferred embodiment, Q is -C(=0)-0-, wherein O is bound to Ar.

In another preferred embodiment, Q is -S(=0)m-C(R7R8)-, wherein S is bound to Ar.

In another preferred embodiment, Q is -S(=0)m-C(R7R8)- , wherein C is bound to Ar.

In another preferred embodiment, Q is -N(R2)-S(=0)m-, wherein N is bound to Ar.

In another preferred embodiment, Q is -N(R2)-S(=0)m-, wherein S is bound to Ar.

In another preferred embodiment, Q is -N(R2)-C(R9R10)-, wherein N is bound to Ar.

In another preferred embodiment, Q is -N(R2)-C(R9R10)-, wherein C is bound to Ar.

In another preferred embodiment, Q is -C(=0)-C(R19R20)-, wherein C(=0) is bound to Ar.

In another preferred embodiment, Q is -C(=0)-C(R19R20)-, wherein C(R19R20) is bound to Ar.

In another preferred embodiment, Q is -N(R2)-C(=0)-, wherein N is bound to Ar.

In another preferred embodiment, Q is -N(R2)-C(=0)-, wherein C is bound to Ar.

In another preferred embodiment, Q is -N(R2)-C(=S)-, wherein N is bound to Ar.

In another preferred embodiment, Q is -N(R2)-C(=S)-, wherein C is bound to Ar.

In another preferred embodiment, Q is -N=C(X)-, wherein N is bound to Ar.

In another preferred embodiment, Q is -N=C(X)-, wherein C is bound to Ar.

In another preferred embodiment, Q is -N(R2)-C(=NR)-, wherein N is bound to Ar.

In another preferred embodiment, Q is -N(R2)-C(=NR)-, wherein C is bound to Ar.

In another preferred embodiment, Q is -C(R13R14)-C(R15R16)-.

In another preferred embodiment, Q is -C(R17)=C(R18)-.

In another preferred embodiment, Q is -C(R4R5)-0-, -N(R2)-S(=0)m-, -N(R2)-C(R9R10)-, -N(R2)-C(=0)-, -N(R2)-C(=S)-, -N=C(X)-, or -N(R2)-C(=NR)-, wherein Ar is bound to either side of Q;

In another preferred embodiment, Q is -C(R4R5)-0-, -N(R2)-C(R9R10)-, -N(R2)-C(=0)-, -N(R2)-C(=NR)-, wherein Ar is bound to either side of Q;

In another preferred embodiment, Q is -C(R4R5)-0-, -N(R2)-C(R9R10)-, or -N(R2)-C(=0)-, wherein Ar is bound to either side of Q;

In another preferred embodiment, Q is-N(R2)-C(R9R10)-, wherein C is bound to Ar, or -N(R2)-C(=0)-, wherein N is bound to Ar, or-C(R4R5)-0-, wherein C is bound to Ar;

In one preferred embodiment, X is H or N(R3)2;

In another preferred embodiment, X is H;

In another preferred embodiment, X is N(R3)2;

In one preferred embodiment, R3 is Ci-C6-alkyl, Ci-C6-alkoxy, C2-C6-alkenyl, C2-C6-alkynyl, Ci-C6-alkoxy-Ci-C4-alkyl, C3-C6-cycloalkyl, C3-C6-cycloalkyl-Ci-C4-alkyl, or C3-C6-cycloalkoxy-Ci-C4-alkyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with halogen,

Ci-C6-alkylene-CN, phenyl, or -Chh-phenyl, wherein the phenyl rings are unsubstituted or substituted with Rf;

In another preferred embodiment, R3 is H, Ci-C6-alkyl, or Ci-C6-alkoxy-Ci-C4-alkyl;

In another preferred embodiment, R3 is H, or Ci-C6-alkyl;

In another preferred embodiment, R3 is Ci-C6-alkyl;

In another preferred embodiment, R3 is H;

In one preferred embodiment, R is H, CN, Ci-C6-alkyl, Ci-C6-haloalkyl, C2-C6-alkenyl, C2-C6-haloalkenyl, C2-C6-alkynyl, C2-C6-haloalkynyl, C3-C6-cycloalkyl, C3-C6-halocycloalkyl, OR8, or N(R3)2;

In another preferred embodiment, R is H, CN, Ci-C6-alkyl, or OR8;

In another preferred embodiment, R is H, or Ci-C6-alkyl;

In another preferred embodiment, R is H, CH3, C2H5, n-C3H7, or isopropyl;

In one preferred embodiment, R6 is H, Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C1-C6-alkoxy-Ci-C4-alkyl, C3-C6-cycloalkyl, C3-C6-cycloalkyl-Ci-C4-alkyl, C3-C6-cycloalkoxy-Ci-C4- alkyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with halogen,

C(=0)-ORa, Ci-C6-alkylene-NRbRc, Ci-C6-alkylene-CN, C(=0)-NRbRc, C(=0)-Rd, S02NRbRc, S(=0)mRe, phenyl, or -CFh-phenyl, wherein the phenyl rings are unsubstituted or substituted with Rf;

In another preferred embodiment, R6 is H, Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C1-C6-alkoxy-Ci-C4-alkyl, C3-C6-cycloalkyl, C3-C6-cycloalkyl-Ci-C4-alkyl, C3-C6-cycloalkoxy-Ci-C4-alkyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with halogen,

In another preferred embodiment, R6 is C(=0)-ORa, Ci-C6-alkylene-NRbRc, Ci-C6-alkylene-CN, C(=0)-NRbRc, C(=0)-Rd, S02NRbRc, S(=0)mRe, phenyl, or -CH2-phenyl, wherein the phenyl rings are unsubstituted or substituted with Rf;

In another preferred embodiment, R6 is H, Ci-C6-alkyl, Ci-C6-haloalkyl, -CH2-C(=0)-ORa, or -CH2-phenyl;

In another preferred embodiment, R6 is H, Ci-C6-alkyl, Ci-C6-haloalkyl, or -CH2-phenyl;

In another preferred embodiment, R6 is H, Ci-C6-alkyl, Ci-C6-haloalkyl, or -CH2-C(=0)-ORa;

In another preferred embodiment, R6 is H, Ci-C6-alkyl, or Ci-C6-haloalkyl;

In another preferred embodiment, R6 is H;

In another preferred embodiment, R6 is Ci-C6-alkyl;

In another preferred embodiment, R6 is Ci-C6-haloalkyl;

In another preferred embodiment, R6 is H, CH3, C2H5, CH2CF3, or CHF2;

In another preferred embodiment, R6 is H, CH3, C2H5, or CH2CF3;

In one preferred embodiment, R4, R5, R7, R8, R9, R10, R13, R14, R15, R16, R17, R18, R19, R20 are, identical or different, H, halogen, Ci-C6-alkyl, Ci-C6-haloalkylalkyl, C2-C6-alkenyl, C2-C6-alkynyl, Ci-C6-alkoxy-Ci-C4-alkyl, C3-C6-cycloalkyl, C3-C6-halocycloalkyl,C3-C6-cycloalkyl-Ci-C4-alkyl, C3-C6-cycloalkoxy-Ci-C4-alkyl, C(=0)-ORa, C(=0)-NRbRc, C(=0)-Rd, S02NRbRc, S(=0)mRe, phenyl, or -CH2-phenyl, wherein the phenyl rings are unsubstituted or substituted with Rf;

In another preferred embodiment, R4, R5, R7, R8, R9, R10, R13, R14, R15, R16, R17, R18, R19, R20 are, identical or different, H, halogen, Ci-C6-alkyl, Ci-C6-haloalkylalkyl, C3-C6-cycloalkyl, C3-C6-halocycloalkyl, C(=0)-ORa, C(=0)-NRbRc, C(=0)-Rd, phenyl, or -CH2-phenyl, wherein the phenyl rings are unsubstituted or substituted with Rf;

In another preferred embodiment, R4, R5, R7, R8, R9, R10, R13, R14, R15, R16, R17, R18, R19, R20 are, identical or different, H, halogen, Ci-C6-alkyl, or Ci-C6-haloalkylalkyl;

In another preferred embodiment, R4, R5, R7, R8, R9, R10, R13, R14, R15, R16, R17, R18, R19, R20 are, identical or different, H, halogen, or Ci-C6-alkyl;

In another preferred embodiment, R4, R5, R7, R8, R9, R10, R13, R14, R15, R16, R17, R18, R19, R20 are, identical or different, H or Ci-C6-alkyl;

In one preferred embodiment, Ar is phenyl which is unsubstituted or substituted with RAr.

In another preferred embodiment, Ar is 5- or 6-membered hetaryl, which is unsubstituted or substituted with RAr.

In more preferred embodiment, Ar is phenyl, pyrimidinyl, pyridazinyl, or pyridyl, which are unsubstituted or substituted with RAr.

In one preferred embodiment, RAr is halogen, OH, CN, NO2, SCN, Ci-C6-alkyl, C1-C6-haloalkyl, Ci-C6-alkoxy, Ci-C6-haloalkoxy, or S-Re.

In more preferred embodiment, RAr is F, Cl , Br, OH, CN, NO2, SCN, CH3, C2H5, n-C3H7, isopropyl, CH2F, CHF2, CF3, CH2CF3, CF2CHF2, C2F5, CH2CH2CF3, CH2CF2CHF2,

CH2CF2CF3, OCH3, OC2H5, n-propyloxy, isopropyloxy, OCH2F, OCHF2, OCF3, OCH2CF3, OCF2CHF2, OC2F5, OCH2CH2CF3, OCH2CF2CHF2, OCH2CF2CF3, or S-Re, where Re is Cr C6-alkyl, in particular Ci-C3-alkyl such as CH3, C2H5, n-C3H7 or isopropyl, or Ci-C6-haloalkyl, in particular fluorinated Ci-C3-alkyl such as CH2F, CHF2, CF3, CH2CF3, CF2CHF2, C2F5, CH2CH2CF3, CH2CF2CHF2 or CH2CF2CF3.

Perticularly preferred Ar are listed in Table A below.

Table A:

Particularly preferred Ar is selected from Ar-1 to Ar-20;

also particularly preferred Ar is selected from Ar-1 to Ar-13;

also particularly preferred Ar is selected from Ar-1 to Ar-13 and Ar-17 to Ar-18;

also particularly preferred Ar is selected from Ar-1 , Ar-2, Ar-3, Ar-4, Ar-10, Ar-17, and Ar-18. also particularly preferred Ar is Ar-2;

also particularly preferred Ar is selected from Ar-17 and Ar-18;

also particularly preferred Ar is Ar-17;

also particularly preferred Ar is Ar-18;

In one preferred embodiment, R1 is Y-Z-T-R11.

In another preferred embodiment, R1 is Y-Z-T-R12.

In one preferred embodiment, Y is -CRya=N-, wherein the N is bound to Z.

In another preferred embodiment, Y is -NRyc-C(=S)-, wherein C(=S) is bound to Z.

In another preferred embodiment, Y is -NRyc-C(=0)-, wherein C(=0) is bound to Z.

In one preferred embodiment, Z is a single bond;

-NRzc-C(=0)-, wherein C(=0) is bound to T;

-NRZC-C(=S)-, wherein C(=S) is bound to T;

-N=C(S-Rza)-, wherein T is bound to the carbon atom; or

-NRzc-C(S-Rza)=, wherein T is bound to the carbon atom;

In another preferred embodiment, Z is -NRZC-C(=S)-, wherein C(=S) is bound to T.

In another preferred embodiment, Z is -NRzc-C(=0)-, wherein C(=0) is bound to T.

In another preferred embodiment, Z is-N=C(S-Rza)-, wherein T is bound to the carbon atom.

In another preferred embodiment, Z is-NRzc-C(S-Rza)=, wherein T is bound to the carbon atom.

In another preferred embodiment, Z is -0-C(=0)-, wherein T is bound to the carbon atom;

In another preferred embodiment, Z is a single bond.

In one preferred embodiment, T is O.

In another preferred embodiment, T is N-RT.

In another preferred embodiment, T is N.

In one preferred embodiment, Rya is H, halogen, Ci-C6-alkyl, Ci-C6-alkoxy, which are unsubstituted or substituted with halogen,

phenyl, or -CFh-phenyl, wherein the phenyl rings are unsubstituted or substituted with Rf.

In more preferred embodiment, Rya is H, halogen, Ci-C6-alkyl, Ci-C6-alkoxy, which are unsubstituted or substituted with halogen,

, or phenyl which is unsubstituted or substituted with Rf.

In most preferred embodiment, Rya is H, F, Cl , Br, CH3, C2H5, n-C3H7, isopropyl, CH2F, CHF2, CFS, CH2CF3, CF2CHF2, C2F5, CH2CH2CF3, CH2CF2CHF2, CH2CF2CF3, OCH3, OC2H5, n-propyloxy, isopropyloxy, OCH2F, OCHF2, OCF3, OCH2CF3, OCF2CHF2, OC2F5,

OCH2CH2CF3, OCH2CF2CHF2, OCH2CF2CF3, or phenyl which is unsubstituted or substituted with Rf.

In further most preferred embodiment, Rya is H or CH3;

In one embodiment, Ryc, Rzc independently are H, Ci-C6-alkyl, C3-C6-cycloalkyl, which are unsubstituted or substiuted with halogen,

phenyl, or -CFh-phenyl, wherein the rings are unsubstituted or substituted with Rf.

In more preferred embodiment, Rycand Rzc are H, Ci-C6-alkyl, Ci-C6-haloalkyl, or phenyl which is unsubstituted or substituted with Rf.

In most preferred embodiment, Rycand Rzcare H, CH3, C2H5, n-C3H7, isopropyl, CH2F,

CHF2, CFS, CH2CF3, CF2CHF2, C2F5, CH2CH2CF3, CH2CF2CHF2, CH2CF2CF3, or phenyl which is unsubstituted or substituted with Rf.

In further most preferred embodiment, Rycand Rzcare H or CH3;

In one preferred embodiment, RT is H, Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, Ci-C4-alkyl-Ci-C6-alkoxy, which are unsubstituted or substituted with halogen,

C(=0)-NRbRc, C(=0)-Rd, S02NRbRc, S(=0)mRe, phenyl, or -CH2-phenyl, wherein the phenyl rings are unsubstituted or substituted with Rf.

In more preferred embodiment, RT is H, Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C1-C4-alkyl-Ci-C6-alkoxy, which are unsubstituted or substituted with halogen.

In most preferred embodiment, RT is H or Ci-C6-alkyl.

In another preferred embodiment, Rzc together with RT if present, forms Ci-C6-alkylene or a linear C2-C6-alkenylene group, where in the linear Ci-C6-alkylene and the linear C2-C6-alkenylene a CH2 moiety may be replaced by a carbonyl or a C=N-R' and/or wherein 1 or 2 CH2 moieties may be replaced by O or S and/or wherein the linear Ci-C6-alkylene and the linear C2-C6-alkenylene may be unsubstituted or substituted with Rh.

In more preferred embodiment, Rzc together with RT if present, forms Ci-C6-alkylene or a linear C2-C6-alkenylene group, where in the linear Ci-C6-alkylene and the linear C2-C6-alkenylene a CH2 moiety is replaced by a carbonyl group.

In another more preferred embodiment, Rzc together with RT if present, forms C1-C6-alkylene or a linear C2-C6-alkenylene group, where in the linear Ci-C6-alkylene and the linear C2-C6-alkenylene a CH2 moiety is replaced by a C=N-R' and wherein 1 or 2 CH2 moieties may be replaced by O or S and/or wherein the linear Ci-C6-alkylene and the linear C2-C6-alkenylene may be unsubstituted or substituted with Rh.

In another more preferred embodiment, Rzc together with RT if present, forms C1-C6-alkylene or a linear C2-C6-alkenylene group, where in the linear Ci-C6-alkylene and the linear C2-C6-alkenylene 1 or 2 CH2 moieties are replaced by O or S and/or wherein the linear C1-C6-alkylene and the linear C2-C6-alkenylene may be unsubstituted or substituted with Rh.

In one preferred embodiment, Rza is H, Ci-C6-alkyl, Ci-C6-haloalkyl, Ci-C6-alkylene-NRbRc, C1-C6- C(=0)-Rd, phenyl, phenylcarbonyl, or -CH2-phenyl, wherein the phenyl rings are unsubstituted or substituted with Rf;

In more preferred embodiment, Rza is H, Ci-C6-alkyl, or Ci-C6-haloalkyl;

In most preferred embodiment, Rza is H, Ci-C6-alkyl.

In another preferred embodiment, Rza together with RT if present, forms Ci-C6-alkylene or a linear C2-C6-alkenylene group, where in the linear Ci-C6-alkylene and the linear C2-C6-alkenylene a CH2 moiety may be replaced by a carbonyl or a C=N-R' and/or wherein 1 or 2 CH2 moieties may be replaced by O or S and/or wherein the linear Ci-C6-alkylene and the linear C2-C6-alkenylene may be unsubstituted or substituted with Rh;

In more preferred embodiment, Rza together with RT if present, forms Ci-C6-alkylene or a linear C2-C6-alkenylene group, where in the linear Ci-C6-alkylene and the linear C2-C6-alkenylene a CH2 moiety is replaced by a carbonyl group.

In another more preferred embodiment, Rza together with RT if present, forms C1-C6-alkylene or a linear C2-C6-alkenylene group, where in the linear Ci-C6-alkylene and the linear C2-C6-alkenylene a CH2 moiety is replaced by a C=N-R' and wherein 1 or 2 CH2 moieties

may be replaced by O or S and/or wherein the linear Ci-C6-alkylene and the linear C2-C6-alkenylene may be unsubstituted or substituted with Rh.

In another more preferred embodiment, Rza together with RT if present, forms C1-C6-alkylene or a linear C2-C6-alkenylene group, where in the linear Ci-C6-alkylene and the linear C2-C6-alkenylene 1 or 2 CH2 moieties are replaced by O or S and/or wherein the linear C1-C6-alkylene and the linear C2-C6-alkenylene may be unsubstituted or substituted with Rh.

In a preferred embodiment, Ra, Rb and Rc are H, Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, which are unsubstituted or substituted with halogen,

Ci-C6-alkylene-CN, phenyl, or -Chh-phenyl, wherein the phenyl rings are unsubstituted or substituted with Rf;

In more preferred embodiment, Ra, Rb and Rc are H, Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, which are unsubstituted or substituted with halogen,

phenyl, or -Chh-phenyl, wherein the phenyl rings are unsubstituted or substituted with Rf.

In a preferred embodiment, Rd is H, Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, which are unsubstituted or substituted with halogen,

phenyl, or -Chh-phenyl, wherein the phenyl rings are unsubstituted or substituted with Rf.

In more preferred embodiment, Rd is H, Ci-C6-alkyl, Ci-C6-haloalkyl, or phenyl which is unsubstituted or substituted with Rf.

In one preferred embodiment, Re is Ci-C6-alkyl, Ci-C6-haloalkyl, C3-C6-cycloalkyl, C3-C6-halocycloalkyl, phenyl, or -Chh-phenyl, wherein the phenyl rings are unsubstituted or substituted with Rf.

In more preferred embodiment, Re is H, Ci-C6-alkyl, Ci-C6-haloalkyl, or phenyl unsubstituted or substituted with Rf.

In one preferred embodiment, Rf is halogen, N3, OH, CN, NO2, -SCN, -SF5, Ci-C6-alkyl, Ci-C6-alkoxy, C2-C6-alkenyl, C2-C6-alkynyl, C3-C6-cycloalkyl, C3-C6-cycloalkoxy, which are unsubstituted or substituted with halogen,

C(=0)-ORa, NRbRc, Ci-C6-alkylene-NRbRc, Ci-C6-alkylene-CN, C(=0)-NRbRc, C(=0)-Rd, S02NRbRc, or S(=0)mRe.

In more preferred embodiment, Rf is halogen, N3, OH, CN, Ci-C6-alkyl, Ci-C6-alkoxy, C2-C6-alkenyl, C2-C6-alkynyl, C3-C6-cycloalkyl, C3-C6-cycloalkoxy, which are unsubstituted or substituted with halogen,

C(=0)-ORa, NRbRc, Ci-C6-alkylene-NRbRc, Ci-C6-alkylene-CN, C(=0)-NRbRc, C(=0)-Rd, S02NRbRc, or S(=0)mRe.

In a preferred embodiment, R9 is halogen, N3, OH, CN, NO2, -SCN, -SF5, Ci-C6-alkyl, C1-C6-alkoxy, C2-C6-alkenyl, C2-C6-alkynyl, C3-C6-cycloalkyl, C3-C6-cycloalkoxy, which are unsubstituted or substituted with halogen,

C(=0)-0Ra, NRbRc, Ci-C6-alkylene-NRbRc, NH-Ci-C6-alkylene-NRbRc, C(=0)-NRbRc, C(=0)-Rd, S02NRbRc, or S(=0)mRe.

In more preferred embodiment, R9 is halogen, N3, OH, CN, NO2, Ci-C6-alkyl, Ci-C6-alkoxy, C2-C6-alkenyl, C3-C6-cycloalkyl, C3-C6-cycloalkoxy, which are unsubstituted or substituted with halogen,

C(=0)-0Ra, NRbRc, Ci-C6-alkylene-NRbRc, C(=0)-NRbRc, C(=0)-Rd, S02NRbRc, or S(=0)mRe. In one embodiment, m is 0.

In another embodiment, m is 1.

In another embodiment, m is 2.

In another embodiment, m is 0 or 1.

In another embodiment, m is 1 or 2.

In more preferred embodiment, R1 are formulas Y-1 to Y-9 wherein V denotes attachment to the 10 membered hetaryl, D is R11 or R12 and wherein RT, R11, R12, Rya, Ryc, Rza and Rzc are as defined in compounds of formula I.


In more preferred embodiment, R1 are formulas Y-1 to Y-8 wherein ^ denotes attachment to the 10 membered hetaryl, D is R11 or R12 and wherein RT, R11, R12, Rya, Ryc, Rza and Rzc are as defined in compounds of formula I.

Y

In another more preferred embodiment, R1 are formulas YZT-1 to YZT-9, wherein ' de notes attachment to the 10 membered hetaryl and R11, R12, RT, Rya, Rza and Rzc are as de fined in compounds of formula I.

In another more preferred embodiment, R1 are formulas YZT-1 to YZT-8, wherein ^ de notes attachment to the 10 membered hetaryl and R11, R12, RT, Rya, Rza and Rzc are as de fined in compounds of formula I.

In another more preferred embodiment, R1 are formulas YZT-1 , YZT-5, YZT-6, or YZT-8,

wherein V denotes attachment to the 10 membered hetaryl and R11, R12, RT, Rya, Rza and Rzc are as defined in compounds of formula I.

In most preferred embodiment, R1 are formulas Y-1 A to Y-9A, wherein Y denotes attach-ment to the 10 membered hetaryl, D is R11 or R12.

In most preferred embodiment, R1 are formulas Y-1 A to Y-8B, wherein
denotes attach-ment to the 10 membered hetaryl, D is R11 or R12.

In most preferred embodiment, R1 are formulas Y-1A, Y-5A, Y-6A, or Y-8A,, wherein
denotes attachment to the 10 membered hetaryl, D is R11 or R12.

In one preferred embodiment, R11 is Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, Ci-C6-alkoxy-Ci-C4-alkyl, C3-C6-cycloalkyl, C3-C6-cycloalkyl-Ci-C4-alkyl, Ci-C4-alkyl-C3-C6-cycloalkoxy, which are unsubstituted or substituted with halogen,

aryl, arylcarbonyl, aryl-Ci-C4-alkyl, aryloxy-Ci-C4-alkyl, hetaryl, carbonylhetaryl, Ci-C4-alkyl-hetaryl and Ci-C4-alkyl-hetaryloxy, wherein the aryl or hetaryl rings are unsubstituted or substituted with R9 and wherein the hetaryl is a 5- or 6-membered monocyclic hetaryl or a 8-, 9- or 10-membered bicyclic hetaryl.

In more preferred embodiment, R11 is Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C3-C6-cycloalkyl, which are unsubstituted or substituted with halogen,

aryl, arylcarbonyl, aryl-Ci-C4-alkyl, aryloxy-Ci-C4-alkyl, hetaryl, carbonylhetaryl, Ci-C4-alkyl-hetaryl and Ci-C4-alkyl-hetaryloxy, where the rings are unsubstituted or substituted with R9 and wherein the hetaryl is a 5- or 6-membered monocyclic hetaryl or a 8-, 9- or 10-membered bicyclic hetaryl.

In most preferred embodiment, R11 is aryl, aryl-Ci-C4-alkyl, hetaryl, or hetaryl-Ci-C4-alkyl, wherein the rings are unsubstituted or substituted with R9 and where hetaryl in hetaryl or hetaryl-Ci-C4-alkyl, is preferably a 5- or 6-membered monocyclic hetaryl such as pyridyl, pyrimidinyl, pyridazinyl, pyrrolyl, pyrazolyl, imidazolyl, oxazolyl, thiazolyl, isoxazolyl or isothiazolyl which is unsubstituted or substituted with R9.

Examples of particularly preferred radicals R11 are the radicals R11-1 to R11-29 summarized in Table A-1 below.

Table A-1 .




In another preferred embodiment, R11 is R11-1 or R11-29;

In another preferred embodiment, R11 is R11-1 ;

In one embodiment, R12 is a radical of the formula (A1),


wherein # indicates the point of attachment to T and wherein R121, R122, R123and R124 are as defined above and wherein R121, R122, R123and R124 independently of each other and especially in combination preferably have the following meanings:

R121 is Ci-C4-alkoxy, in particular OCH3, OC2H5;

R122 is Ci-C4-alkoxy, such as OCH3, OC2H5, n-propoxyx or isopropoxy, or C3-C4- alkenyloxy, such as allyloxy, with R122 in particular being OCH3, OC2H5, or n- propoxy;

R123 is OH, Ci-C4-alkoxy, such as OCH3, OC2H5,, or C3-C4-alkenyloxy, such as

allyloxy, with R123 in particular being OCH3, OC2H5;

R124 is Ci-C4-alkyl, such as CH3 or C2H5, or Ci-C4-alkoxy-Ci-C4-alkyl, such as

methoxymethyl, ethoxymethyl, 2-methoxyethyl or 2-ethoxyethyl, with R124 in particular being methyl;.

In more preferred embodiment, R12 is in particular a radical of the formula (A11), e.g. (A11-a) or (A11-b)


wherein # indicates the point of attachment to T and wherein R121, R122, R123and R124 are as defined above and wherein R121, R122, R123and R124 independently of each other and especially in combination preferably have the following meanings:

R121 is Ci-C4-alkoxy, in particular OCH3 or OC2H5;

R122 is Ci-C4-alkoxy, such as OCH3, OC2H5, n-propoxyx or isopropoxy, or C3-C4- alkenyloxy, such as allyloxy, with R122 in particular being OCH3, OC2H5 or n- propoxy;

R123 is OH, Ci-C4-alkoxy, such as OCH3 or OC2H5, or C3-C4-alkenyloxy, such as

allyloxy, with R123 in particular being OCH3 or OC2H5;

R124 is Ci-C4-alkyl, such as CH3 or C2H5, or Ci-C4-alkoxy-Ci-C4-alkyl, such as

methoxymethyl, ethoxymethyl, 2-methoxyethyl or 2-ethoxyethyl, with R124 in particular being methyl.

Particular examples of radicals R12 are the following radicals A11-1 , A11-1 a, A11-1 b, A11-2, A11-2a, A11-2b, A11-3, A11-3a and A11-3b:

In another preferred embodiment compounds of formula I, R12 is A11, preferably A11-1 ;

In another preferred embodiment compounds of formula I are selected from compounds of formula I.A to I.F;


wherein, Ar is phenyl or 5- or 6-membered hetaryl ring which is substituted with RAr;

RAr is halogen, OH, CN, NO2, SCN, Ci-C6-alkyl, Ci-C6-alkoxy, or S-Re, wherein the alkyl and alkoxy are unsubstituted or substituted with halogen;

B1 is CRB1;

B2 is CRB2;

B3 is CRB3;

RB1, RB2, and RB3 independently of each other are H, halogen, or Ci-C6-alkyl;

Q is -C(R4R5)-0-, -N(R2)-S(=0)m-, -N(R2)-C(R9R10)-, -N(R2)-C(=0)-, -N(R2)-C(=S)-, -N=C(X)-, -N(R2)-C(=NR)-; wherein Ar is bound to either side of Q;

X is N(R3)2;

and R1 is Y-Z-T-R11 or Y-Z-T-R12, as defined in formula I.

also In a more preferred embodiment compounds of formula I are compounds of formula I.A or I.F, wherein Ar is phenyl or 5- or 6-membered hetaryl ring which is substituted with RAr;

RAr is halogen, OH, CN, NO2, SCN, Ci-C6-alkyl, Ci-C6-alkoxy, or S-Re, wherein the alkyl and alkoxy are unsubstituted or substituted with halogen;

B1 is CRB1;

B2 is CRB2;

B3 is CRB3;

RB1, RB2, and RB3 independently of each other are H, halogen, or Ci-C6-alkyl;

Ar is Ar1, Ar2, Ar3, Ar4, Ar10, Ar17, or Ar18;

Q is -C(R4R5)-0-, -N(R2)-C(R9R10)-, or -N(R2)-C(=0)-; wherein Ar is bound to either side of Q;

R1 are formulas YZT-1 , YZT-5, YZT-6, or YZT-8;

In another preferred embodiment of compounds of formula I, wherein

A1 is N or CRA1;

A2 is N or CRA2;

A3 is N or CRA3;

wherein at least one of the A1, A2, A3 is N;

B1 is CRB1, B2 is CRB2, B3 is CRB3;

RB1, RB2, RB3 independently of each other are H, halogen, or Ci-C6-alkyl;

Q is -C(R4R5)-0-, -N(R2)-C(R9R10)-, or -N(R2)-C(=0)-; wherein Ar is bound to either side of Q;

Ar is Ar1, Ar2, Ar3, Ar4, Ar10, Ar17, or Ar18;

R1 are formulas Y-1A, Y-5A, Y-6A, or Y-8A, wherein D is R11 or R12;

R11 is selected from R11-1 to R11-29

R12 is A11 ; preferably A11-1 ;

In another preferred embodiment of compounds of formula I, wherein

A1 is N, A2 is CRA2, and A3 is N; or A1 is CRA1, A2 is N, and A3 is N; or A1 is CRA1, A2 is CRA2, and A3 is N;

B1 is CRB1, B2 is CRB2, B3 is CRB3;

RB1, RB2, R 63 are H;

Ar is Ar2;

Q is -N(R2)-C(R9R10)-, wherein C is bound to Ar; or

Q is -N(R2)-C(=0)-, wherein N is bound to Ar; or

Q is -C(R4R5)-0-, wherein C is bound to Ar;

R1 are formulas Y-1A, Y-5A, Y-6A, or Y-8A, wherein D is R11 or R12;

R11 is R11-1 or R11-29;

R12 is A11-1 ;

more preferred compounds of formula I are selected from compounds of formula 1.1 A to I.6C as shown below, wherein R1 is selected from Y-1 A, Y-1 B, Y-2A, Y-2B, Y-3A, Y-3B, Y-3C, Y-3D, Y-4A, Y-4B, Y-4C, Y-4D, Y-5A, Y-5B, Y-6A, Y-6B, Y-7A, Y-7B, Y-8A, and Y-8B; wherein D is R11 or R12, and other variables are as defined herein.

Also more preferred compound of formula I are formulae 1.1 to 1.6, wherein

B1 is CRB1, B2 is CRB2, B3 is CRB3,

RB1, RB2, and RB3 independently of each other are H, halogen, Ci-C6-alkyl;

Q is -C(R4R5)-0-, -N(R2)-C(R9R10)-, -N(R2)-C(=0)-, -N(R2)-C(=NR)-; wherein Ar is bound to either side of Q;

m is 0, 1 , or 2;

R is H, CN, or Ci-C6-alkyl;

R2 is H or Ci-C6-alkyl;

R4, R5, R9, R10, are identical or different H or Ci-C6-alkyl;

R6 is H, Ci-C6-alkyl, Ci-C6-haloalkyl, or -Chh-phenyl;

Ar is Ar1, Ar2, Ar3, Ar4, Ar10, Ar17, or Ar18;

R1 is Y-1 A, Y-3C, Y-5A, Y-6A, Y-7A, Y-8A, or Y-9A;

D is R11 or R12;

R11 is R11-1 or R11-10;

R12 is A11-1 b or A11-3b;

In another preferred embodiment, the compound of formula I are selected from compounds of formula 1.1 to 1.48, wherein the variables are as defined in the compound of formula I;

wo 2020/109039 45

In another preferred embodiment, the compound of formula I are selected from compounds of formula 1.1 to 1.48, wherein

Ar is Ar1 , Ar2, Ar3, Ar4, Ar10, Ar17, or Ar18;

B1 is CH;

B2 is CH;

B3 is CH;

R1 is Y-1 A, Y-1 B, Y-2A, Y-2B, Y-3A, Y-3B, Y-3C, Y-3D, Y-4A, Y-4B, Y-4C, Y-4D, Y-5A, Y-5B, Y-6A, Y-6B, Y-7A, Y-7B, Y-8A, or Y-8B; wherein D is R11 or R12;

R11 is R11-1 , R11-2, R11-3, R11-4, R11-5, R11-6, R11-7, R11-8, R11-9, R11-10, R11-1 1 , R11-12, R11-13, R11-14, R11-15, R11-16, R11-17, R11-18, R11-19, R11-20, R11-21 , R11-22, R11-23, R11-24, R11-25, R11-26, R11-27, R11-28, or R11-29;

R12 is (A11-1 ), (A11-2), or (A11-3).

R4 and R5 independently are H or CH3,

R9 and R10 independently are H or CH3,

R2 is H, CHs, or c-CsHs

R is NH, NCHs, or NCN;

Particular compounds of formula I are the compounds of the formulae 1.1 to 1.24 that are compiled in the following tables 1 to 2160, wherein the term Formula denotes compounds of formula, and wherein combination of variables B1 , B2, B3, Ar, and D for each compound of tables 1 to 2160 corresponds to each line of Table B. Each of the groups mentioned for a substituent in the tables is furthermore per se, independently of the combination in which it is mentioned, a particularly preferred aspect of the substituent in question.

Table 1 . Formula 1.1 wherein R1 is Y-1 A, R4 is H and R5 is H.

Table 2. Formula 1.1 wherein R1 is Y-1 B, R4 is H and R5 is H.

Table 3. Formula 1.1 wherein R1 is Y-2A, R4 is H and R5 is H.

Table 4. Formula 1.1 wherein R1 is Y-2B, R4 is H and R5 is H.

Table 5. Formula 1.1 wherein R1 is Y-3A, R4 is H and R5 is H.

Table 6. Formula 1.1 wherein R1 is Y-3B, R4 is H and R5 is H.

Table 7. Formula 1.1 wherein R1 is Y-3C, R4 is H and R5 is H.

Table 8. Formula 1.1 wherein R1 is Y-3D, R4 is H and R5 is H.

Table 9. Formula 1.1 wherein R1 is Y-4A, R4 is H and R5 is H.

Table 10. Formula 1.1 wherein R1 is Y-4B, R4 is H and R5 is H. Table 1 1 . Formula 1.1 wherein R1 is Y-4C, R4 is H and R5 is H. Table 12. Formula 1.1 wherein R1 is Y-4D, R4 is H and R5 is H. Table 13. Formula 1.1 wherein R1 is Y-5A, R4 is H and R5 is H. Table 14. Formula 1.1 wherein R1 is Y-5B, R4 is H and R5 is H. Table 15. Formula 1.1 wherein R1 is Y-6A, R4 is H and R5 is H. Table 16. Formula 1.1 wherein R1 is Y-6B, R4 is H and R5 is H. Table 17. Formula 1.1 wherein R1 is Y-7A, R4 is H and R5 is H. Table 18. Formula 1.1 wherein R1 is Y-7B, R4 is H and R5 is H. Table 19. Formula 1.1 wherein R1 is Y-8A, R4 is H and R5 is H. Table 20. Formula 1.1 wherein R1 is Y-8B, R4 is H and R5 is H. Table 21 . Formula 1.1 wherein R1 is Y-1A, R4 is CHs and R5 is H. Table 22. Formula 1.1 wherein R1 is Y-1 B, R4 is CH3 and R5 is H. Table 23. Formula 1.1 wherein R1 is Y-2A, R4 is CH3 and R5 is H. Table 24. Formula 1.1 wherein R1 is Y-2B, R4 is CH3 and R5 is H. Table 25. Formula 1.1 wherein R1 is Y-3A, R4 is CH3 and R5 is H. Table 26. Formula 1.1 wherein R1 is Y-3B, R4 is CH3 and R5 is H. Table 27. Formula 1.1 wherein R1 is Y-3C, R4 is CH3 and R5 is H. Table 28. Formula 1.1 wherein R1 is Y-3D, R4 is CH3 and R5 is H. Table 29. Formula 1.1 wherein R1 is Y-4A, R4 is CH3 and R5 is H. Table 30. Formula 1.1 wherein R1 is Y-4B, R4 is CH3 and R5 is H. Table 31 . Formula 1.1 wherein R1 is Y-4C, R4 is CH3 and R5 is H. Table 32. Formula 1.1 wherein R1 is Y-4D, R4 is CH3 and R5 is H. Table 33. Formula 1.1 wherein R1 is Y-5A, R4 is CH3 and R5 is H. Table 34. Formula 1.1 wherein R1 is Y-5B, R4 is CH3 and R5 is H. Table 35. Formula 1.1 wherein R1 is Y-6A, R4 is CH3 and R5 is H. Table 36. Formula 1.1 wherein R1 is Y-6B, R4 is CH3 and R5 is H. Table 37. Formula 1.1 wherein R1 is Y-7A, R4 is CH3 and R5 is H. Table 38. Formula 1.1 wherein R1 is Y-7B, R4 is CH3 and R5 is H. Table 39. Formula 1.1 wherein R1 is Y-8A, R4 is CH3 and R5 is H. Table 40. Formula 1.1 wherein R1 is Y-8B, R4 is CH3 and R5 is H. Table 41 . Formula 1.1 wherein R1 is Y-1 A, R4 is CH3 and R5 is CH3. Table 42. Formula 1.1 wherein R1 is Y-1 B, R4 is CH3 and R5 is CH3. Table 43. Formula 1.1 wherein R1 is Y-2A, R4 is CH3 and R5 is CH3.

Table 44. Formula 1.1 wherein R1 is Y-2B, R4 is CH3 and R5 is CH3. Table 45. Formula 1.1 wherein R1 is Y-3A, R4 is CH3 and R5 is CH3. Table 46. Formula 1.1 wherein R1 is Y-3B, R4 is CH3 and R5 is CH3. Table 47. Formula 1.1 wherein R1 is Y-3C, R4 is CH3 and R5 is CH3. Table 48. Formula 1.1 wherein R1 is Y-3D, R4 is CH3 and R5 is CH3. Table 49. Formula 1.1 wherein R1 is Y-4A, R4 is CH3 and R5 is CH3. Table 50. Formula 1.1 wherein R1 is Y-4B, R4 is CH3 and R5 is CH3. Table 51 . Formula 1.1 wherein R1 is Y-4C, R4 is CH3 and R5 is CH3. Table 52. Formula 1.1 wherein R1 is Y-4D, R4 is CH3 and R5 is CH3. Table 53. Formula 1.1 wherein R1 is Y-5A, R4 is CH3 and R5 is CH3. Table 54. Formula 1.1 wherein R1 is Y-5B, R4 is CH3 and R5 is CH3. Table 55. Formula 1.1 wherein R1 is Y-6A, R4 is CH3 and R5 is CH3. Table 56. Formula 1.1 wherein R1 is Y-6B, R4 is CH3 and R5 is CH3. Table 57. Formula 1.1 wherein R1 is Y-7A, R4 is CH3 and R5 is CH3. Table 58. Formula 1.1 wherein R1 is Y-7B, R4 is CH3 and R5 is CH3. Table 59. Formula 1.1 wherein R1 is Y-8A, R4 is CH3 and R5 is CH3. Table 60. Formula 1.1 wherein R1 is Y-8B, R4 is CH3 and R5 is CH3. Table 61 . Formula I.2 wherein R1 is Y-1A, R4 is H and R5 is H. Table 62. Formula 1.2 wherein R1 is Y-1 B, R4 is H and R5 is H. Table 63. Formula I.2 wherein R1 is Y-2A, R4 is H and R5 is H. Table 64. Formula I.2 wherein R1 is Y-2B, R4 is H and R5 is H. Table 65. Formula I.2 wherein R1 is Y-3A, R4 is H and R5 is H. Table 66. Formula I.2 wherein R1 is Y-3B, R4 is H and R5 is H. Table 67. Formula I.2 wherein R1 is Y-3C, R4 is H and R5 is H. Table 68. Formula I.2 wherein R1 is Y-3D, R4 is H and R5 is H. Table 69. Formula I.2 wherein R1 is Y-4A, R4 is H and R5 is H. Table 70. Formula I.2 wherein R1 is Y-4B, R4 is H and R5 is H. Table 71 . Formula I.2 wherein R1 is Y-4C, R4 is H and R5 is H. Table 72. Formula I.2 wherein R1 is Y-4D, R4 is H and R5 is H. Table 73. Formula I.2 wherein R1 is Y-5A, R4 is H and R5 is H. Table 74. Formula I.2 wherein R1 is Y-5B, R4 is H and R5 is H. Table 75. Formula I.2 wherein R1 is Y-6A, R4 is H and R5 is H. Table 76. Formula I.2 wherein R1 is Y-6B, R4 is H and R5 is H. Table 77. Formula I.2 wherein R1 is Y-7A, R4 is H and R5 is H. Table 78. Formula I.2 wherein R1 is Y-7B, R4 is H and R5 is H. Table 79. Formula I.2 wherein R1 is Y-8A, R4 is H and R5 is H.

Table 80. Formula 1.2 wherein R1 is Y-8B, R4 is H and R5 is H.

Table 81 . Formula 1.2 wherein R1 is Y-1 A, R4 is CH3 and R5 is H.

Table 82. Formula 1.2 wherein R1 is Y-1 B, R4 is CH3 and R5 is H.

Table 83. Formula 1.2 wherein R1 is Y-2A, R4 is CH3 and R5 is H.

Table 84. Formula 1.2 wherein R1 is Y-2B, R4 is CH3 and R5 is H.

Table 85. Formula 1.2 wherein R1 is Y-3A, R4 is CH3 and R5 is H.

Table 86. Formula 1.2 wherein R1 is Y-3B, R4 is CH3 and R5 is H.

Table 87. Formula 1.2 wherein R1 is Y-3C, R4 is CH3 and R5 is H.

Table 88. Formula 1.2 wherein R1 is Y-3D, R4 is CH3 and R5 is H.

Table 89. Formula 1.2 wherein R1 is Y-4A, R4 is CH3 and R5 is H.

Table 90. Formula 1.2 wherein R1 is Y-4B, R4 is CH3 and R5 is H.

Table 91 . Formula 1.2 wherein R1 is Y-4C, R4 is CH3 and R5 is H.

Table 92. Formula 1.2 wherein R1 is Y-4D, R4 is CH3 and R5 is H.

Table 93. Formula 1.2 wherein R1 is Y-5A, R4 is CH3 and R5 is H.

Table 94. Formula 1.2 wherein R1 is Y-5B, R4 is CH3 and R5 is H.

Table 95. Formula 1.2 wherein R1 is Y-6A, R4 is CH3 and R5 is H.

Table 96. Formula 1.2 wherein R1 is Y-6B, R4 is CH3 and R5 is H.

Table 97. Formula 1.2 wherein R1 is Y-7A, R4 is CH3 and R5 is H.

Table 98. Formula 1.2 wherein R1 is Y-7B, R4 is CH3 and R5 is H.

Table 99. Formula 1.2 wherein R1 is Y-8A, R4 is CH3 and R5 is H.

Table 100. Formula 1.2 wherein R1 is Y-8B, R4 is CH3 and R5 is H.

Table 101 . Formula 1.2 wherein R1 is Y-1 A, R4 is CH3 and R5 is CH3.

Table 102. Formula 1.2 wherein R1 is Y-1 B, R4 is CH3 and R5 is CH3.

Table 103. Formula 1.2 wherein R1 is Y-2A, R4 is CH3 and R5 is CH3.

Table 104. Formula 1.2 wherein R1 is Y-2B, R4 is CH3 and R5 is CH3.

Table 105. Formula 1.2 wherein R1 is Y-3A, R4 is CH3 and R5 is CH3.

Table 106. Formula 1.2 wherein R1 is Y-3B, R4 is CH3 and R5 is CH3.

Table 107. Formula 1.2 wherein R1 is Y-3C, R4 is CH3 and R5 is CH3.

Table 108. Formula 1.2 wherein R1 is Y-3D, R4 is CH3 and R5 is CH3.

Table 109. Formula 1.2 wherein R1 is Y-4A, R4 is CH3 and R5 is CH3.

Table 1 10. Formula 1.2 wherein R1 is Y-4B, R4 is CH3 and R5 is CH3.

Table 1 1 1 . Formula 1.2 wherein R1 is Y-4C, R4 is CH3 and R5 is CH3.

Table 1 12. Formula 1.2 wherein R1 is Y-4D, R4 is CH3 and R5 is CH3.

Table 1 13. Formula 1.2 wherein R1 is Y-5A, R4 is CH3 and R5 is CH3.

Table 1 14. Formula 1.2 wherein R1 is Y-5B, R4 is CH3 and R5 is CH3.

Table 1 15. Formula 1.2 wherein R1 is Y-6A, R4 is CH3 and R5 is CH3.

Table 1 16. Formula 1.2 wherein R 1 is Y-6B, R4 is CH3 and R5 is CH3. Table 1 17. Formula 1.2 wherein R 1 is Y-7A, R4 is CH3 and R5 is CH3. Table 1 18. Formula 1.2 wherein R 1 is Y-7B, R4 is CH3 and R5 is CH3. Table 1 19. Formula 1.2 wherein R 1 is Y-8A, R4 is CH3 and R5 is CH3. Table 120. Formula 1.2 wherein R 1 is Y-8B, R4 is CH3 and R5 is CH3. Table 121 . Formula 1.5 wherein R 1 is Y-1A, R4 is H and R5 is H. Table 122. Formula 1.5 wherein R 1 is Y-1 B, R4 is H and R5 is H. Table 123. Formula 1.5 wherein R 1 is Y-2A, R4 is H and R5 is H. Table 124. Formula 1.5 wherein R 1 is Y-2B, R4 is H and R5 is H. Table 125. Formula 1.5 wherein R 1 is Y-3A, R4 is H and R5 is H. Table 126. Formula 1.5 wherein R 1 is Y-3B, R4 is H and R5 is H. Table 127. Formula 1.5 wherein R 1 is Y-3C, R4 is H and R5 is H. Table 128. Formula 1.5 wherein R 1 is Y-3D, R4 is H and R5 is H. Table 129. Formula 1.5 wherein R 1 is Y-4A, R4 is H and R5 is H. Table 130. Formula 1.5 wherein R 1 is Y-4B, R4 is H and R5 is H. Table 131 . Formula 1.5 wherein R 1 is Y-4C, R4 is H and R5 is H. Table 132. Formula 1.5 wherein R 1 is Y-4D, R4 is H and R5 is H. Table 133. Formula 1.5 wherein R 1 is Y-5A, R4 is H and R5 is H. Table 134. Formula 1.5 wherein R 1 is Y-5B, R4 is H and R5 is H. Table 135. Formula 1.5 wherein R 1 is Y-6A, R4 is H and R5 is H. Table 136. Formula 1.5 wherein R 1 is Y-6B, R4 is H and R5 is H. Table 137. Formula 1.5 wherein R 1 is Y-7A, R4 is H and R5 is H. Table 138. Formula 1.5 wherein R 1 is Y-7B, R4 is H and R5 is H. Table 139. Formula 1.5 wherein R 1 is Y-8A, R4 is H and R5 is H. Table 140. Formula 1.5 wherein R 1 is Y-8B, R4 is H and R5 is H. Table 141 . Formula 1.5 wherein R 1 is Y-1A, R4 is CH3 and R5 is H. Table 142. Formula 1.5 wherein R 1 is Y-1 B, R4 is CH3 and R5 is H. Table 143. Formula 1.5 wherein R 1 is Y-2A, R4 is CH3 and R5 is H. Table 144. Formula 1.5 wherein R 1 is Y-2B, R4 is CH3 and R5 is H. Table 145. Formula 1.5 wherein R 1 is Y-3A, R4 is CH3 and R5 is H. Table 146. Formula 1.5 wherein R 1 is Y-3B, R4 is CH3 and R5 is H. Table 147. Formula 1.5 wherein R 1 is Y-3C, R4 is CH3 and R5 is H. Table 148. Formula 1.5 wherein R 1 is Y-3D, R4 is CH3 and R5 is H. Table 149. Formula 1.5 wherein R 1 is Y-4A, R4 is CH3 and R5 is H. Table 150. Formula 1.5 wherein R 1 is Y-4B, R4 is CH3 and R5 is H. Table 151 . Formula 1.5 wherein R 1 is Y-4C, R4 is CH3 and R5 is H.

Table 152. Formula 1.5 wherein R1 is Y-4D, R4 is CH3 and R5 is H. Table 153. Formula 1.5 wherein R1 is Y-5A, R4 is CH3 and R5 is H. Table 154. Formula 1.5 wherein R1 is Y-5B, R4 is CH3 and R5 is H. Table 155. Formula 1.5 wherein R1 is Y-6A, R4 is CH3 and R5 is H. Table 156. Formula 1.5 wherein R1 is Y-6B, R4 is CH3 and R5 is H. Table 157. Formula 1.5 wherein R1 is Y-7A, R4 is CH3 and R5 is H. Table 158. Formula 1.5 wherein R1 is Y-7B, R4 is CH3 and R5 is H. Table 159. Formula 1.5 wherein R1 is Y-8A, R4 is CH3 and R5 is H. Table 160. Formula 1.5 wherein R1 is Y-8B, R4 is CH3 and R5 is H. Table 161 . Formula 1.5 wherein R1 is Y-1 A, R4 is CH3 and R5 is CH3. Table 162. Formula 1.5 wherein R1 is Y-1 B, R4 is CH3 and R5 is CH3. Table 163. Formula 1.5 wherein R1 is Y-2A, R4 is CH3 and R5 is CH3. Table 164. Formula 1.5 wherein R1 is Y-2B, R4 is CH3 and R5 is CH3. Table 165. Formula 1.5 wherein R1 is Y-3A, R4 is CH3 and R5 is CH3. Table 166. Formula 1.5 wherein R1 is Y-3B, R4 is CH3 and R5 is CH3. Table 167. Formula 1.5 wherein R1 is Y-3C, R4 is CH3 and R5 is CH3. Table 168. Formula 1.5 wherein R1 is Y-3D, R4 is CH3 and R5 is CH3. Table 169. Formula 1.5 wherein R1 is Y-4A, R4 is CH3 and R5 is CH3. Table 170. Formula 1.5 wherein R1 is Y-4B, R4 is CH3 and R5 is CH3. Table 171 . Formula 1.5 wherein R1 is Y-4C, R4 is CH3 and R5 is CH3. Table 172. Formula 1.5 wherein R1 is Y-4D, R4 is CH3 and R5 is CH3. Table 173. Formula 1.5 wherein R1 is Y-5A, R4 is CH3 and R5 is CH3. Table 174. Formula 1.5 wherein R1 is Y-5B, R4 is CH3 and R5 is CH3. Table 175. Formula 1.5 wherein R1 is Y-6A, R4 is CH3 and R5 is CH3. Table 176. Formula 1.5 wherein R1 is Y-6B, R4 is CH3 and R5 is CH3. Table 177. Formula 1.5 wherein R1 is Y-7A, R4 is CH3 and R5 is CH3. Table 178. Formula 1.5 wherein R1 is Y-7B, R4 is CH3 and R5 is CH3. Table 179. Formula 1.5 wherein R1 is Y-8A, R4 is CH3 and R5 is CH3. Table 180. Formula 1.5 wherein R1 is Y-8B, R4 is CH3 and R5 is CH3. Table 181 . Formula 1.6 wherein R1 is Y-1 A, R4 is H and R5 is H. Table 182. Formula 1.6 wherein R1 is Y-1 B, R4 is H and R5 is H. Table 183. Formula 1.6 wherein R1 is Y-2A, R4 is H and R5 is H. Table 184. Formula 1.6 wherein R1 is Y-2B, R4 is H and R5 is H. Table 185. Formula 1.6 wherein R1 is Y-3A, R4 is H and R5 is H. Table 186. Formula 1.6 wherein R1 is Y-3B, R4 is H and R5 is H. Table 187. Formula 1.6 wherein R1 is Y-3C, R4 is H and R5 is H.

Table 188. Formula 1.6 wherein R 1 is Y-3D, R4 is H and R5 is H. Table 189. Formula 1.6 wherein R 1 is Y-4A, R4 is H and R5 is H. Table 190. Formula 1.6 wherein R 1 is Y-4B, R4 is H and R5 is H. Table 191 . Formula 1.6 wherein R 1 is Y-4C, R4 is H and R5 is H. Table 192. Formula 1.6 wherein R 1 is Y-4D, R4 is H and R5 is H. Table 193. Formula 1.6 wherein R 1 is Y-5A, R4 is H and R5 is H. Table 194. Formula 1.6 wherein R 1 is Y-5B, R4 is H and R5 is H. Table 195. Formula 1.6 wherein R 1 is Y-6A, R4 is H and R5 is H. Table 196. Formula 1.6 wherein R 1 is Y-6B, R4 is H and R5 is H. Table 197. Formula 1.6 wherein R 1 is Y-7A, R4 is H and R5 is H. Table 198. Formula 1.6 wherein R 1 is Y-7B, R4 is H and R5 is H. Table 199. Formula 1.6 wherein R 1 is Y-8A, R4 is H and R5 is H. Table 200. Formula 1.6 wherein R 1 is Y-8B, R4 is H and R5 is H. Table 201 . Formula 1.6 wherein R 1 is Y-1A, R4 is CHs and R5 is H. Table 202. Formula 1.6 wherein R 1 is Y-1 B, R4 is CH3 and R5 is H. Table 203. Formula 1.6 wherein R 1 is Y-2A, R4 is CH3 and R5 is H. Table 204. Formula 1.6 wherein R 1 is Y-2B, R4 is CH3 and R5 is H. Table 205. Formula 1.6 wherein R 1 is Y-3A, R4 is CH3 and R5 is H. Table 206. Formula 1.6 wherein R 1 is Y-3B, R4 is CH3 and R5 is H. Table 207. Formula 1.6 wherein R 1 is Y-3C, R4 is CH3 and R5 is H. Table 208. Formula 1.6 wherein R 1 is Y-3D, R4 is CH3 and R5 is H. Table 209. Formula 1.6 wherein R 1 is Y-4A, R4 is CH3 and R5 is H. Table 210. Formula 1.6 wherein R 1 is Y-4B, R4 is CH3 and R5 is H. Table 21 1 . Formula 1.6 wherein R 1 is Y-4C, R4 is CH3 and R5 is H. Table 212. Formula 1.6 wherein R 1 is Y-4D, R4 is CH3 and R5 is H. Table 213. Formula 1.6 wherein R 1 is Y-5A, R4 is CH3 and R5 is H. Table 214. Formula 1.6 wherein R 1 is Y-5B, R4 is CH3 and R5 is H. Table 215. Formula 1.6 wherein R 1 is Y-6A, R4 is CH3 and R5 is H. Table 216. Formula 1.6 wherein R 1 is Y-6B, R4 is CH3 and R5 is H. Table 217. Formula 1.6 wherein R 1 is Y-7A, R4 is CH3 and R5 is H. Table 218. Formula 1.6 wherein R 1 is Y-7B, R4 is CH3 and R5 is H. Table 219. Formula 1.6 wherein R 1 is Y-8A, R4 is CH3 and R5 is H. Table 220. Formula 1.6 wherein R 1 is Y-8B, R4 is CH3 and R5 is H. Table 221 . Formula 1.6 wherein R 1 is Y-1 A, R4 is CH3 and R5 is CH3. Table 222. Formula 1.6 wherein R 1 is Y-1 B, R4 is CH3 and R5 is CH3. Table 223. Formula 1.6 wherein R 1 is Y-2A, R4 is CH3 and R5 is CH3.

Table 224. Formula 1.6 wherein R1 is Y-2B, R4 is CH3 and R5 is CH3. Table 225. Formula 1.6 wherein R1 is Y-3A, R4 is CH3 and R5 is CH3. Table 226. Formula 1.6 wherein R1 is Y-3B, R4 is CH3 and R5 is CH3. Table 227. Formula 1.6 wherein R1 is Y-3C, R4 is CH3 and R5 is CH3. Table 228. Formula 1.6 wherein R1 is Y-3D, R4 is CH3 and R5 is CH3. Table 229. Formula 1.6 wherein R1 is Y-4A, R4 is CH3 and R5 is CH3. Table 230. Formula 1.6 wherein R1 is Y-4B, R4 is CH3 and R5 is CH3. Table 231 . Formula 1.6 wherein R1 is Y-4C, R4 is CH3 and R5 is CH3. Table 232. Formula 1.6 wherein R1 is Y-4D, R4 is CH3 and R5 is CH3. Table 233. Formula 1.6 wherein R1 is Y-5A, R4 is CH3 and R5 is CH3. Table 234. Formula 1.6 wherein R1 is Y-5B, R4 is CH3 and R5 is CH3. Table 235. Formula 1.6 wherein R1 is Y-6A, R4 is CH3 and R5 is CH3. Table 236. Formula 1.6 wherein R1 is Y-6B, R4 is CH3 and R5 is CH3. Table 237. Formula 1.6 wherein R1 is Y-7A, R4 is CH3 and R5 is CH3. Table 238. Formula 1.6 wherein R1 is Y-7B, R4 is CH3 and R5 is CH3. Table 239. Formula 1.6 wherein R1 is Y-8A, R4 is CH3 and R5 is CH3. Table 240. Formula 1.6 wherein R1 is Y-8B, R4 is CH3 and R5 is CH3. Table 241 . Formula 1.7 wherein R1 is Y-1A, R4 is H and R5 is H. Table 242. Formula 1.7 wherein R1 is Y-1 B, R4 is H and R5 is H. Table 243. Formula 1.7 wherein R1 is Y-2A, R4 is H and R5 is H. Table 244. Formula 1.7 wherein R1 is Y-2B, R4 is H and R5 is H. Table 245. Formula 1.7 wherein R1 is Y-3A, R4 is H and R5 is H. Table 246. Formula 1.7 wherein R1 is Y-3B, R4 is H and R5 is H. Table 247. Formula 1.7 wherein R1 is Y-3C, R4 is H and R5 is H. Table 248. Formula 1.7 wherein R1 is Y-3D, R4 is H and R5 is H. Table 249. Formula 1.7 wherein R1 is Y-4A, R4 is H and R5 is H. Table 250. Formula 1.7 wherein R1 is Y-4B, R4 is H and R5 is H. Table 251 . Formula 1.7 wherein R1 is Y-4C, R4 is H and R5 is H. Table 252. Formula 1.7 wherein R1 is Y-4D, R4 is H and R5 is H. Table 253. Formula 1.7 wherein R1 is Y-5A, R4 is H and R5 is H. Table 254. Formula 1.7 wherein R1 is Y-5B, R4 is H and R5 is H. Table 255. Formula 1.7 wherein R1 is Y-6A, R4 is H and R5 is H. Table 256. Formula 1.7 wherein R1 is Y-6B, R4 is H and R5 is H. Table 257. Formula 1.7 wherein R1 is Y-7A, R4 is H and R5 is H. Table 258. Formula 1.7 wherein R1 is Y-7B, R4 is H and R5 is H. Table 259. Formula 1.7 wherein R1 is Y-8A, R4 is H and R5 is H.

Table 260. Formula 1.7 wherein R1 is Y-8B, R4 is H and R5 is H. Table 261 . Formula 1.7 wherein R1 is Y-1A, R4 is CHs and R5 is H. Table 262. Formula 1.7 wherein R1 is Y-1 B, R4 is CH3 and R5 is H. Table 263. Formula 1.7 wherein R1 is Y-2A, R4 is CH3 and R5 is H. Table 264. Formula 1.7 wherein R1 is Y-2B, R4 is CH3 and R5 is H. Table 265. Formula 1.7 wherein R1 is Y-3A, R4 is CH3 and R5 is H. Table 266. Formula 1.7 wherein R1 is Y-3B, R4 is CH3 and R5 is H. Table 267. Formula 1.7 wherein R1 is Y-3C, R4 is CH3 and R5 is H. Table 268. Formula 1.7 wherein R1 is Y-3D, R4 is CH3 and R5 is H. Table 269. Formula 1.7 wherein R1 is Y-4A, R4 is CH3 and R5 is H. Table 270. Formula 1.7 wherein R1 is Y-4B, R4 is CH3 and R5 is H. Table 271 . Formula 1.7 wherein R1 is Y-4C, R4 is CH3 and R5 is H. Table 272. Formula 1.7 wherein R1 is Y-4D, R4 is CH3 and R5 is H. Table 273. Formula 1.7 wherein R1 is Y-5A, R4 is CH3 and R5 is H. Table 274. Formula 1.7 wherein R1 is Y-5B, R4 is CH3 and R5 is H. Table 275. Formula 1.7 wherein R1 is Y-6A, R4 is CH3 and R5 is H. Table 276. Formula 1.7 wherein R1 is Y-6B, R4 is CH3 and R5 is H. Table 277. Formula 1.7 wherein R1 is Y-7A, R4 is CH3 and R5 is H. Table 278. Formula 1.7 wherein R1 is Y-7B, R4 is CH3 and R5 is H. Table 279. Formula 1.7 wherein R1 is Y-8A, R4 is CH3 and R5 is H. Table 280. Formula 1.7 wherein R1 is Y-8B, R4 is CH3 and R5 is H. Table 281 . Formula 1.7 wherein R1 is Y-1 A, R4 is CH3 and R5 is CH3. Table 282. Formula 1.7 wherein R1 is Y-1 B, R4 is CH3 and R5 is CH3. Table 283. Formula 1.7 wherein R1 is Y-2A, R4 is CH3 and R5 is CH3. Table 284. Formula 1.7 wherein R1 is Y-2B, R4 is CH3 and R5 is CH3. Table 285. Formula 1.7 wherein R1 is Y-3A, R4 is CH3 and R5 is CH3. Table 286. Formula 1.7 wherein R1 is Y-3B, R4 is CH3 and R5 is CH3. Table 287. Formula 1.7 wherein R1 is Y-3C, R4 is CH3 and R5 is CH3. Table 288. Formula 1.7 wherein R1 is Y-3D, R4 is CH3 and R5 is CH3. Table 289. Formula 1.7 wherein R1 is Y-4A, R4 is CH3 and R5 is CH3. Table 290. Formula 1.7 wherein R1 is Y-4B, R4 is CH3 and R5 is CH3. Table 291 . Formula 1.7 wherein R1 is Y-4C, R4 is CH3 and R5 is CH3. Table 292. Formula 1.7 wherein R1 is Y-4D, R4 is CH3 and R5 is CH3. Table 293. Formula 1.7 wherein R1 is Y-5A, R4 is CH3 and R5 is CH3. Table 294. Formula 1.7 wherein R1 is Y-5B, R4 is CH3 and R5 is CH3. Table 295. Formula 1.7 wherein R1 is Y-6A, R4 is CH3 and R5 is CH3.

Table 296. Formula 1.7 wherein R 1 is Y-6B, R4 is CH3 and R5 is CH3. Table 297. Formula 1.7 wherein R 1 is Y-7A, R4 is CH3 and R5 is CH3. Table 298. Formula 1.7 wherein R 1 is Y-7B, R4 is CH3 and R5 is CH3. Table 299. Formula 1.7 wherein R 1 is Y-8A, R4 is CH3 and R5 is CH3. Table 300. Formula 1.7 wherein R 1 is Y-8B, R4 is CH3 and R5 is CH3. Table 301 . Formula 1.8 wherein R 1 is Y-1A, R4 is H and R5 is H. Table 302. Formula 1.8 wherein R 1 is Y-1 B, R4 is H and R5 is H. Table 303. Formula 1.8 wherein R 1 is Y-2A, R4 is H and R5 is H. Table 304. Formula 1.8 wherein R 1 is Y-2B, R4 is H and R5 is H. Table 305. Formula 1.8 wherein R 1 is Y-3A, R4 is H and R5 is H. Table 306. Formula 1.8 wherein R 1 is Y-3B, R4 is H and R5 is H. Table 307. Formula 1.8 wherein R 1 is Y-3C, R4 is H and R5 is H. Table 308. Formula 1.8 wherein R 1 is Y-3D, R4 is H and R5 is H. Table 309. Formula 1.8 wherein R 1 is Y-4A, R4 is H and R5 is H. Table 310. Formula 1.8 wherein R 1 is Y-4B, R4 is H and R5 is H. Table 31 1 . Formula 1.8 wherein R 1 is Y-4C, R4 is H and R5 is H. Table 312. Formula 1.8 wherein R 1 is Y-4D, R4 is H and R5 is H. Table 313. Formula 1.8 wherein R 1 is Y-5A, R4 is H and R5 is H. Table 314. Formula 1.8 wherein R 1 is Y-5B, R4 is H and R5 is H. Table 315. Formula 1.8 wherein R 1 is Y-6A, R4 is H and R5 is H. Table 316. Formula 1.8 wherein R 1 is Y-6B, R4 is H and R5 is H. Table 317. Formula 1.8 wherein R 1 is Y-7A, R4 is H and R5 is H. Table 318. Formula 1.8 wherein R 1 is Y-7B, R4 is H and R5 is H. Table 319. Formula 1.8 wherein R 1 is Y-8A, R4 is H and R5 is H. Table 320. Formula 1.8 wherein R 1 is Y-8B, R4 is H and R5 is H. Table 321 . Formula 1.8 wherein R 1 is Y-1A, R4 is CH3 and R5 is H. Table 322. Formula 1.8 wherein R 1 is Y-1 B, R4 is CH3 and R5 is H. Table 323. Formula 1.8 wherein R 1 is Y-2A, R4 is CH3 and R5 is H. Table 324. Formula 1.8 wherein R 1 is Y-2B, R4 is CH3 and R5 is H. Table 325. Formula 1.8 wherein R 1 is Y-3A, R4 is CH3 and R5 is H. Table 326. Formula 1.8 wherein R 1 is Y-3B, R4 is CH3 and R5 is H. Table 327. Formula 1.8 wherein R 1 is Y-3C, R4 is CH3 and R5 is H. Table 328. Formula 1.8 wherein R 1 is Y-3D, R4 is CH3 and R5 is H. Table 329. Formula 1.8 wherein R 1 is Y-4A, R4 is CH3 and R5 is H. Table 330. Formula 1.8 wherein R 1 is Y-4B, R4 is CH3 and R5 is H. Table 331 . Formula 1.8 wherein R 1 is Y-4C, R4 is CH3 and R5 is H.

Table 332. Formula 1.8 wherein R1 is Y-4D, R4 is CH3 and R5 is H.

Table 333. Formula I.8 wherein R1 is Y-5A, R4 is CH3 and R5 is H.

Table 334. Formula I.8 wherein R1 is Y-5B, R4 is CH3 and R5 is H.

Table 335. Formula I.8 wherein R1 is Y-6A, R4 is CH3 and R5 is H.

Table 336. Formula I.8 wherein R1 is Y-6B, R4 is CH3 and R5 is H.

Table 337. Formula I.8 wherein R1 is Y-7A, R4 is CH3 and R5 is H.

Table 338. Formula I.8 wherein R1 is Y-7B, R4 is CH3 and R5 is H.

Table 339. Formula I.8 wherein R1 is Y-8A, R4 is CH3 and R5 is H.

Table 340. Formula I.8 wherein R1 is Y-8B, R4 is CH3 and R5 is H.

Table 341 . Formula I.8 wherein R1 is Y-1A, R4 is CH3 and R5 is CH3.

Table 342. Formula I.8 wherein R1 is Y-1 B, R4 is CH3 and R5 is CH3.

Table 343. Formula 1.8 wherein R1 is Y-2A, R4 is CH3 and R5 is CH3.

Table 344. Formula I.8 wherein R1 is Y-2B, R4 is CH3 and R5 is CH3.

Table 345. Formula 1.8 wherein R1 is Y-3A, R4 is CH3 and R5 is CH3.

Table 346. Formula I.8 wherein R1 is Y-3B, R4 is CH3 and R5 is CH3.

Table 347. Formula I.8 wherein R1 is Y-3C, R4 is CH3 and R5 is CH3.

Table 348. Formula I.8 wherein R1 is Y-3D, R4 is CH3 and R5 is CH3.

Table 349. Formula 1.8 wherein R1 is Y-4A, R4 is CH3 and R5 is CH3.

Table 350. Formula I.8 wherein R1 is Y-4B, R4 is CH3 and R5 is CH3.

Table 351 . Formula 1.8 wherein R1 is Y-4C, R4 is CH3 and R5 is CH3.

Table 352. Formula 1.8 wherein R1 is Y-4D, R4 is CH3 and R5 is CH3.

Table 353. Formula 1.8 wherein R1 is Y-5A, R4 is CH3 and R5 is CH3.

Table 354. Formula I.8 wherein R1 is Y-5B, R4 is CH3 and R5 is CH3.

Table 355. Formula 1.8 wherein R1 is Y-6A, R4 is CH3 and R5 is CH3.

Table 356. Formula I.8 wherein R1 is Y-6B, R4 is CH3 and R5 is CH3.

Table 357. Formula 1.8 wherein R1 is Y-7A, R4 is CH3 and R5 is CH3.

Table 358. Formula I.8 wherein R1 is Y-7B, R4 is CH3 and R5 is CH3.

Table 359. Formula 1.8 wherein R1 is Y-8A, R4 is CH3 and R5 is CH3.

Table 360. Formula I.8 wherein R1 is Y-8B, R4 is CH3 and R5 is CH3.

Table 361 . Formula 1.13 wherein R1 is Y-1 A, R2 is H, R9 is H and R10 is H.

Table 362. Formula 1.13 wherein R1 is Y-1 A, R2 is H, R9 is CH3 and, R10 is H.

Table 363. Formula 1.13 wherein R1 is Y-1 A, R2 is H, R9 is CH3 and R10 is CH3.

Table 364. Formula 1.13 wherein R1 is Y-1 B, R2 is H, R9 is H and R10 is H.

Table 365. Formula 1.13 wherein R1 is Y-1 B, R2 is H, R9 is CH3 and R10 is H.

Table 366. Formula 1.13 wherein R1 is Y-1 B, R2 is H, R9 is CH3 and R10 is CH3.

Table 367. Formula 1.13 wherein R1 is Y-2A, R2 is H, R9 is H and R10 is H.

Table 368. Formula 1.13 wherein R1 is Y-2A, R2 is H, R9 is CH3 and R10 is H.

Table 369. Formula 1.13 wherein R1 is Y-2A, R2 is H, R9 is CH3 and R10 is CH3.

Table 370. Formula 1.13 wherein R1 is Y-2B, R2 is H, R9 is H and R10 is H. Table 371 . Formula 1.13 wherein R1 is Y-2B, R2 is H, R9 is CH3 and R10 is H.

Table 372. Formula 1.13 wherein R1 is Y-2B, R2 is H, R9 is CH3 and R10 is CH3.

Table 373. Formula 1.13 wherein R1 is Y-3A, R2 is H, R9 is H and R10 is H. Table 374. Formula 1.13 wherein R1 is Y-3A, R2 is H, R9 is CH3 and R10 is H.

Table 375. Formula 1.13 wherein R1 is Y-3A, R2 is H, R9 is CH3 and R10 is CH3.

Table 376. Formula 1.13 wherein R1 is Y-3B, R2 is H, R9 is H and R10 is H. Table 377. Formula 1.13 wherein R1 is Y-3B, R2 is H, R9 is CH3 and R10 is H.

Table 378. Formula 1.13 wherein R1 is Y-3B, R2 is H, R9 is CH3 and R10 is CH3.

Table 379. Formula 1.13 wherein R1 is Y-3C, R2 is H, R9 is H and R10 is H. Table 380. Formula 1.13 wherein R1 is Y-3C, R2 is H, R9 is CH3 and R10 is H.

Table 381 . Formula 1.13 wherein R1 is Y-3C, R2 is H, R9 is CH3 and R10 is CH3.

Table 382. Formula 1.13 wherein R1 is Y-3D, R2 is H, R9 is H and R10 is H. Table 383. Formula 1.13 wherein R1 is Y-3D, R2 is H, R9 is CH3 and R10 is H.

Table 384. Formula 1.13 wherein R1 is Y-3D, R2 is H, R9 is CH3 and R10 is CH3.

Table 385. Formula 1.13 wherein R1 is Y-4A, R2 is H, R9 is H and R10 is H. Table 386. Formula 1.13 wherein R1 is Y-4A, R2 is H, R9 is CH3 and R10 is H.

Table 387. Formula 1.13 wherein R1 is Y-4A, R2 is H, R9 is CH3 and R10 is CH3.

Table 388. Formula 1.13 wherein R1 is Y-4B, R2 is H, R9 is H and R10 is H. Table 389. Formula 1.13 wherein R1 is Y-4B, R2 is H, R9 is CH3 and R10 is H.

Table 390. Formula 1.13 wherein R1 is Y-4B, R2 is H, R9 is CH3 and R10 is CH3.

Table 391 . Formula 1.13 wherein R1 is Y-4C, R2 is H, R9 is H and R10 is H. Table 392. Formula 1.13 wherein R1 is Y-4C, R2 is H, R9 is CH3 and R10 is H.

Table 393. Formula 1.13 wherein R1 is Y-4C, R2 is H, R9 is CH3 and R10 is CH3.

Table 394. Formula 1.13 wherein R1 is Y-4D, R2 is H, R9 is H and R10 is H. Table 395. Formula 1.13 wherein R1 is Y-4D, R2 is H, R9 is CH3 and R10 is H.

Table 396. Formula 1.13 wherein R1 is Y-4D, R2 is H, R9 is CH3 and R10 is CH3.

Table 397. Formula 1.13 wherein R1 is Y-5A, R2 is H, R9 is H and R10 is H. Table 398. Formula 1.13 wherein R1 is Y-5A, R2 is H, R9 is CH3 and R10 is H.

Table 399. Formula 1.13 wherein R1 is Y-5A, R2 is H, R9 is CH3 and R10 is CH3.

Table 400. Formula 1.13 wherein R1 is Y-5B, R2 is H, R9 is H and R10 is H. Table 401 . Formula 1.13 wherein R1 is Y-5B, R2 is H, R9 is CH3 and R10 is H.

Table 402. Formula 1.13 wherein R1 is Y-5B, R2 is H, R9 is CH3 and R10 is CH3.

Table 403. Formula 1.13 wherein R1 is Y-6A, R2 is H, R9 is H and R10 is H.

Table 404. Formula 1.13 wherein R1 is Y-6A, R2 is H, R9 is CH3 and R10 is H.

Table 405. Formula 1.13 wherein R1 is Y-6A, R2 is H, R9 is CH3 and R10 is CH3.

Table 406. Formula 1.13 wherein R1 is Y-6B, R2 is H, R9 is H and R10 is H.

Table 407. Formula 1.13 wherein R1 is Y-6B, R2 is H, R9 is CH3 and R10 is H.

Table 408. Formula 1.13 wherein R1 is Y-6B, R2 is H, R9 is CH3 and R10 is CH3.

Table 409. Formula 1.13 wherein R1 is Y-7A, R2 is H, R9 is H and R10 is H.

Table 410. Formula 1.13 wherein R1 is Y-7A, R2 is H, R9 is CH3 and R10 is H.

Table 41 1 . Formula 1.13 wherein R1 is Y-7A, R2 is H, R9 is CH3 and R10 is CH3.

Table 412. Formula 1.13 wherein R1 is Y-7B, R2 is H, R9 is H and R10 is H.

Table 413. Formula 1.13 wherein R1 is Y-7B, R2 is H, R9 is CH3 and R10 is H.

Table 414. Formula 1.13 wherein R1 is Y-7B, R2 is H, R9 is CH3 and R10 is CH3.

Table 415. Formula 1.13 wherein R1 is Y-8A, R2 is H, R9 is H and R10 is H.

Table 416. Formula 1.13 wherein R1 is Y-8A, R2 is H, R9 is CH3 and R10 is H.

Table 417. Formula 1.13 wherein R1 is Y-8A, R2 is H, R9 is CH3 and R10 is CH3.

Table 418. Formula 1.13 wherein R1 is Y-8B, R2 is H, R9 is H and R10 is H.

Table 419. Formula 1.13 wherein R1 is Y-8B, R2 is H, R9 is CH3 and R10 is H.

Table 420. Formula 1.13 wherein R1 is Y-8B, R2 is H, R9 is CH3 and R10 is CH3.

Table 421 . Formula 1.13 wherein R1 is Y-1A, R2 is CH3, R9 is H and R10 is H. Table 422. Formula 1.13 wherein R1 is Y-1A, R2 is CH3, R9 is CH3 and R10 is H.

Table 423. Formula 1.13 wherein R1 is Y-1A, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 424. Formula 1.13 wherein R1 is Y-1 B, R2 is CH3, R9 is H and R10 is H. Table 425. Formula 1.13 wherein R1 is Y-1 B, R2 is CH3, R9 is CH3 and R10 is H.

Table 426. Formula 1.13 wherein R1 is Y-1 B, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 427. Formula 1.13 wherein R1 is Y-2A, R2 is CH3, R9 is H and R10 is H. Table 428. Formula 1.13 wherein R1 is Y-2A, R2 is CH3, R9 is CH3 and R10 is H.

Table 429. Formula 1.13 wherein R1 is Y-2A, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 430. Formula 1.13 wherein R1 is Y-2B, R2 is CH3, R9 is H and R10 is H. Table 431 . Formula 1.13 wherein R1 is Y-2B, R2 is CH3, R9 is CH3 and R10 is H.

Table 432. Formula 1.13 wherein R1 is Y-2B, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 433. Formula 1.13 wherein R1 is Y-3A, R2 is CH3, R9 is H and R10 is H. Table 434. Formula 1.13 wherein R1 is Y-3A, R2 is CH3, R9 is CH3 and R10 is H.

Table 435. Formula 1.13 wherein R1 is Y-3A, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 436. Formula 1.13 wherein R1 is Y-3B, R2 is CH3, R9 is H and R10 is H. Table 437. Formula 1.13 wherein R1 is Y-3B, R2 is CH3, R9 is CH3 and R10 is H.

Table 438. Formula 1.13 wherein R1 is Y-3B, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 439. Formula 1.13 wherein R1 is Y-3C, R2 is CH3, R9 is H and R10 is H.

Table 440. Formula 1.13 wherein R1 is Y-3C, R2 is CH3, R9 is CH3 and R10 is H.

Table 441 . Formula 1.13 wherein R1 is Y-3C, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 442. Formula 1.13 wherein R1 is Y-3D, R2 is CH3, R9 is H and R10 is H. Table 443. Formula 1.13 wherein R1 is Y-3D, R2 is CH3, R9 is CH3 and R10 is H.

Table 444. Formula 1.13 wherein R1 is Y-3D, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 445. Formula 1.13 wherein R1 is Y-4A, R2 is CH3, R9 is H and R10 is H. Table 446. Formula 1.13 wherein R1 is Y-4A, R2 is CH3, R9 is CH3 and R10 is H.

Table 447. Formula 1.13 wherein R1 is Y-4A, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 448. Formula 1.13 wherein R1 is Y-4B, R2 is CH3, R9 is H and R10 is H. Table 449. Formula 1.13 wherein R1 is Y-4B, R2 is CH3, R9 is CH3 and R10 is H.

Table 450. Formula 1.13 wherein R1 is Y-4B, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 451 . Formula 1.13 wherein R1 is Y-4C, R2 is CH3, R9 is H and R10 is H. Table 452. Formula 1.13 wherein R1 is Y-4C, R2 is CH3, R9 is CH3 and R10 is H.

Table 453. Formula 1.13 wherein R1 is Y-4C, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 454. Formula 1.13 wherein R1 is Y-4D, R2 is CH3, R9 is H and R10 is H. Table 455. Formula 1.13 wherein R1 is Y-4D, R2 is CH3, R9 is CH3 and R10 is H.

Table 456. Formula 1.13 wherein R1 is Y-4D, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 457. Formula 1.13 wherein R1 is Y-5A, R2 is CH3, R9 is H and R10 is H. Table 458. Formula 1.13 wherein R1 is Y-5A, R2 is CH3, R9 is CH3 and R10 is H.

Table 459. Formula 1.13 wherein R1 is Y-5A, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 460. Formula 1.13 wherein R1 is Y-5B, R2 is CH3, R9 is H and R10 is H. Table 461 . Formula 1.13 wherein R1 is Y-5B, R2 is CH3, R9 is CH3 and R10 is H.

Table 462. Formula 1.13 wherein R1 is Y-5B, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 463. Formula 1.13 wherein R1 is Y-6A, R2 is CH3, R9 is H and R10 is H. Table 464. Formula 1.13 wherein R1 is Y-6A, R2 is CH3, R9 is CH3 and R10 is H.

Table 465. Formula 1.13 wherein R1 is Y-6A, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 466. Formula 1.13 wherein R1 is Y-6B, R2 is CH3, R9 is H and R10 is H. Table 467. Formula 1.13 wherein R1 is Y-6B, R2 is CH3, R9 is CH3 and R10 is H.

Table 468. Formula 1.13 wherein R1 is Y-6B, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 469. Formula 1.13 wherein R1 is Y-7A, R2 is CH3, R9 is H and R10 is H. Table 470. Formula 1.13 wherein R1 is Y-7A, R2 is CH3, R9 is CH3 and R10 is H.

Table 471 . Formula 1.13 wherein R1 is Y-7A, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 472. Formula 1.13 wherein R1 is Y-7B, R2 is CH3, R9 is H and R10 is H. Table 473. Formula 1.13 wherein R1 is Y-7B, R2 is CH3, R9 is CH3 and R10 is H.

Table 474. Formula 1.13 wherein R1 is Y-7B, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 475. Formula 1.13 wherein R1 is Y-8A, R2 is CH3, R9 is H and R10 is H.

Table 476. Formula 1.13 wherein R1 is Y-8A, R2 is CH3, R9 is CH3 and R10 is H.

Table 477. Formula 1.13 wherein R1 is Y-8A, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 478. Formula 1.13 wherein R1 is Y-8B, R2 is CH3, R9 is H and R10 is H.

Table 479. Formula 1.13 wherein R1 is Y-8B, R2 is CH3, R9 is CH3 and R10 is H.

Table 480. Formula 1.13 wherein R1 is Y-8B, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 481 . Formula 1.13 wherein R1 is Y-1A, R2 is C2H5, R9 is H and R10 is H. Table 482. Formula 1.13 wherein R1 is Y-1A, R2 is C2H5, R9 is CH3 and R10 is H.

Table 483. Formula 1.13 wherein R1 is Y-1A, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 484. Formula 1.13 wherein R1 is Y-1 B, R2 is C2H5, R9 is H and R10 is H. Table 485. Formula 1.13 wherein R1 is Y-1 B, R2 is C2H5, R9 is CH3 and R10 is H.

Table 486. Formula 1.13 wherein R1 is Y-1 B, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 487. Formula 1.13 wherein R1 is Y-2A, R2 is C2H5, R9 is H and R10 is H. Table 488. Formula 1.13 wherein R1 is Y-2A, R2 is C2H5, R9 is CH3 and R10 is H.

Table 489. Formula 1.13 wherein R1 is Y-2A, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 490. Formula 1.13 wherein R1 is Y-2B, R2 is C2H5, R9 is H and R10 is H. Table 491 . Formula 1.13 wherein R1 is Y-2B, R2 is C2H5, R9 is CH3 and R10 is H.

Table 492. Formula 1.13 wherein R1 is Y-2B, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 493. Formula 1.13 wherein R1 is Y-3A, R2 is C2H5, R9 is H and R10 is H. Table 494. Formula 1.13 wherein R1 is Y-3A, R2 is C2H5, R9 is CH3 and R10 is H.

Table 495. Formula 1.13 wherein R1 is Y-3A, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 496. Formula 1.13 wherein R1 is Y-3B, R2 is C2H5, R9 is H and R10 is H. Table 497. Formula 1.13 wherein R1 is Y-3B, R2 is C2H5, R9 is CH3 and R10 is H.

Table 498. Formula 1.13 wherein R1 is Y-3B, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 499. Formula 1.13 wherein R1 is Y-3C, R2 is C2H5, R9 is H and R10 is H. Table 500. Formula 1.13 wherein R1 is Y-3C, R2 is C2H5, R9 is CH3 and R10 is H.

Table 501 . Formula 1.13 wherein R1 is Y-3C, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 502. Formula 1.13 wherein R1 is Y-3D, R2 is C2H5, R9 is H and R10 is H. Table 503. Formula 1.13 wherein R1 is Y-3D, R2 is C2H5, R9 is CH3 and R10 is H.

Table 504. Formula 1.13 wherein R1 is Y-3D, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 505. Formula 1.13 wherein R1 is Y-4A, R2 is C2H5, R9 is H and R10 is H. Table 506. Formula 1.13 wherein R1 is Y-4A, R2 is C2H5, R9 is CH3 and R10 is H.

Table 507. Formula 1.13 wherein R1 is Y-4A, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 508. Formula 1.13 wherein R1 is Y-4B, R2 is C2H5, R9 is H and R10 is H. Table 509. Formula 1.13 wherein R1 is Y-4B, R2 is C2H5, R9 is CH3 and R10 is H.

Table 510. Formula 1.13 wherein R1 is Y-4B, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 51 1 . Formula 1.13 wherein R1 is Y-4C, R2 is C2H5, R9 is H and R10 is H.

Table 512. Formula 1.13 wherein R1 is Y-4C, R2 is C2H5, R9 is CHs and R10 is H. Table 513. Formula 1.13 wherein R1 is Y-4C, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 514. Formula 1.13 wherein R1 is Y-4D, R2 is C2H5, R9 is H and R10 is H.

Table 515. Formula 1.13 wherein R1 is Y-4D, R2 is C2H5, R9 is CH3 and R10 is H. Table 516. Formula 1.13 wherein R1 is Y-4D, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 517. Formula 1.13 wherein R1 is Y-5A, R2 is C2H5, R9 is H and R10 is H.

Table 518. Formula 1.13 wherein R1 is Y-5A, R2 is C2H5, R9 is CH3 and R10 is H. Table 519. Formula 1.13 wherein R1 is Y-5A, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 520. Formula 1.13 wherein R1 is Y-5B, R2 is C2H5, R9 is H and R10 is H.

Table 521 . Formula 1.13 wherein R1 is Y-5B, R2 is C2H5, R9 is CH3 and R10 is H. Table 522. Formula 1.13 wherein R1 is Y-5B, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 523. Formula 1.13 wherein R1 is Y-6A, R2 is C2H5, R9 is H and R10 is H.

Table 524. Formula 1.13 wherein R1 is Y-6A, R2 is C2H5, R9 is CH3 and R10 is H. Table 525. Formula 1.13 wherein R1 is Y-6A, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 526. Formula 1.13 wherein R1 is Y-6B, R2 is C2H5, R9 is H and R10 is H.

Table 527. Formula 1.13 wherein R1 is Y-6B, R2 is C2H5, R9 is CH3 and R10 is H. Table 528. Formula 1.13 wherein R1 is Y-6B, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 529. Formula 1.13 wherein R1 is Y-7A, R2 is C2H5, R9 is H and R10 is H.

Table 530. Formula 1.13 wherein R1 is Y-7A, R2 is C2H5, R9 is CH3 and R10 is H. Table 531 . Formula 1.13 wherein R1 is Y-7A, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 532. Formula 1.13 wherein R1 is Y-7B, R2 is C2H5, R9 is H and R10 is H.

Table 533. Formula 1.13 wherein R1 is Y-7B, R2 is C2H5, R9 is CH3 and R10 is H. Table 534. Formula 1.13 wherein R1 is Y-7B, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 535. Formula 1.13 wherein R1 is Y-8A, R2 is C2H5, R9 is H and R10 is H.

Table 536. Formula 1.13 wherein R1 is Y-8A, R2 is C2H5, R9 is CH3 and R10 is H. Table 537. Formula 1.13 wherein R1 is Y-8A, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 538. Formula 1.13 wherein R1 is Y-8B, R2 is C2H5, R9 is H and R10 is H.

Table 539. Formula 1.13 wherein R1 is Y-8B, R2 is C2H5, R9 is CH3 and R10 is H. Table 540. Formula 1.13 wherein R1 is Y-8B, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 541 . Formula 1.13 wherein R1 is Y-1A, R2 is C-C3H5, R9 is H and R10 is H. Table 542. Formula 1.13 wherein R1 is Y-1A, R2 is C-C3H5, R9 is CH3 and R10 is H. Table 543. Formula 1.13 wherein R1 is Y-1A, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 544. Formula 1.13 wherein R1 is Y-1 B, R2 is C-C3H5, R9 is H and R10 is H. Table 545. Formula 1.13 wherein R1 is Y-1 B, R2 is C-C3H5, R9 is CH3, R10 is H.

Table 546. Formula 1.13 wherein R1 is Y-1 B, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 547. Formula 1.13 wherein R1 is Y-2A, R2 is C-C3H5, R9 is H and R10 is H.

Table 548. Formula 1.13 wherein R1 is Y-2A, R2 is C-C3H5, R9 is CHs and R10 is H. Table 549. Formula 1.13 wherein R1 is Y-2A, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 550. Formula 1.13 wherein R1 is Y-2B, R2 is C-C3H5, R9 is H and R10 is H. Table 551 . Formula 1.13 wherein R1 is Y-2B, R2 is C-C3H5, R9 is CHs and R10 is H. Table 552. Formula 1.13 wherein R1 is Y-2B, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 553. Formula 1.13 wherein R1 is Y-3A, R2 is C-C3H5, R9 is H and R10 is H. Table 554. Formula 1.13 wherein R1 is Y-3A, R2 is C-C3H5, R9 is CHs and R10 is H. Table 555. Formula 1.13 wherein R1 is Y-3A, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 556. Formula 1.13 wherein R1 is Y-3B, R2 is C-C3H5, R9 is H and R10 is H. Table 557. Formula 1.13 wherein R1 is Y-3B, R2 is C-C3H5, R9 is CHs and R10 is H. Table 558. Formula 1.13 wherein R1 is Y-3B, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 559. Formula 1.13 wherein R1 is Y-3C, R2 is C-C3H5, R9 is H and R10 is H. Table 560. Formula 1.13 wherein R1 is Y-3C, R2 is C-C3H5, R9 is CHs and R10 is H. Table 561 . Formula 1.13 wherein R1 is Y-3C, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 562. Formula 1.13 wherein R1 is Y-3D, R2 is C-C3H5, R9 is H and R10 is H. Table 563. Formula 1.13 wherein R1 is Y-3D, R2 is C-C3H5, R9 is CHs and R10 is H. Table 564. Formula 1.13 wherein R1 is Y-3D, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 565. Formula 1.13 wherein R1 is Y-4A, R2 is C-C3H5, R9 is H and R10 is H. Table 566. Formula 1.13 wherein R1 is Y-4A, R2 is C-C3H5, R9 is CHs and R10 is H. Table 567. Formula 1.13 wherein R1 is Y-4A, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 568. Formula 1.13 wherein R1 is Y-4B, R2 is C-C3H5, R9 is H and R10 is H. Table 569. Formula 1.13 wherein R1 is Y-4B, R2 is C-C3H5, R9 is CHs and R10 is H. Table 570. Formula 1.13 wherein R1 is Y-4B, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 571 . Formula 1.13 wherein R1 is Y-4C, R2 is C-C3H5, R9 is H and R10 is H. Table 572. Formula 1.13 wherein R1 is Y-4C, R2 is C-C3H5, R9 is CHs and R10 is H. Table 573. Formula 1.13 wherein R1 is Y-4C, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 574. Formula 1.13 wherein R1 is Y-4D, R2 is C-C3H5, R9 is H and R10 is H. Table 575. Formula 1.13 wherein R1 is Y-4D, R2 is C-C3H5, R9 is CHs and R10 is H. Table 576. Formula 1.13 wherein R1 is Y-4D, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 577. Formula 1.13 wherein R1 is Y-5A, R2 is C-C3H5, R9 is H and R10 is H. Table 578. Formula 1.13 wherein R1 is Y-5A, R2 is C-C3H5, R9 is CHs and R10 is H. Table 579. Formula 1.13 wherein R1 is Y-5A, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 580. Formula 1.13 wherein R1 is Y-5B, R2 is C-C3H5, R9 is H and R10 is H. Table 581 . Formula 1.13 wherein R1 is Y-5B, R2 is C-C3H5, R9 is CHs and R10 is H. Table 582. Formula 1.13 wherein R1 is Y-5B, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 583. Formula 1.13 wherein R1 is Y-6A, R2 is C-C3H5, R9 is H and R10 is H.

Table 584. Formula 1.13 wherein R1 is Y-6A, R2 is C-C3H5, R9 is CHs and R10 is H. Table 585. Formula 1.13 wherein R1 is Y-6A, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 586. Formula 1.13 wherein R1 is Y-6B, R2 is C-C3H5, R9 is H and R10 is H. Table 587. Formula 1.13 wherein R1 is Y-6B, R2 is C-C3H5, R9 is CHs and R10 is H. Table 588. Formula 1.13 wherein R1 is Y-6B, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 589. Formula 1.13 wherein R1 is Y-7A, R2 is C-C3H5, R9 is H and R10 is H. Table 590. Formula 1.13 wherein R1 is Y-7A, R2 is C-C3H5, R9 is CHs and R10 is H. Table 591 . Formula 1.13 wherein R1 is Y-7A, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 592. Formula 1.13 wherein R1 is Y-7B, R2 is C-C3H5, R9 is H and R10 is H. Table 593. Formula 1.13 wherein R1 is Y-7B, R2 is C-C3H5, R9 is CHs and R10 is H. Table 594. Formula 1.13 wherein R1 is Y-7B, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 595. Formula 1.13 wherein R1 is Y-8A, R2 is C-C3H5, R9 is H and R10 is H. Table 596. Formula 1.13 wherein R1 is Y-8A, R2 is C-C3H5, R9 is CHs and R10 is H. Table 597. Formula 1.13 wherein R1 is Y-8A, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 598. Formula 1.13 wherein R1 is Y-8B, R2 is C-C3H5, R9 is H and R10 is H. Table 599. Formula 1.13 wherein R1 is Y-8B, R2 is C-C3H5, R9 is CHs and R10 is H. Table 600. Formula 1.13 wherein R1 is Y-8B, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 601 . Formula 1.14 wherein R1 is Y-1A, R2 is H, R9 is H and R10 is H.

Table 602. Formula 1.14 wherein R1 is Y-1A, R2 is H, R9 is CHs and, R10 is H.

Table 603. Formula 1.14 wherein R1 is Y-1A, R2 is H, R9 is CHs and R10 is CH3. Table 604. Formula 1.14 wherein R1 is Y-1 B, R2 is H, R9 is H and R10 is H.

Table 605. Formula 1.14 wherein R1 is Y-1 B, R2 is H, R9 is CHs and R10 is H.

Table 606. Formula 1.14 wherein R1 is Y-1 B, R2 is H, R9 is CHs and R10 is CH3. Table 607. Formula 1.14 wherein R1 is Y-2A, R2 is H, R9 is H and R10 is H.

Table 608. Formula 1.14 wherein R1 is Y-2A, R2 is H, R9 is CHs and R10 is H.

Table 609. Formula 1.14 wherein R1 is Y-2A, R2 is H, R9 is CHs and R10 is CH3. Table 610. Formula 1.14 wherein R1 is Y-2B, R2 is H, R9 is H and R10 is H.

Table 61 1 . Formula 1.14 wherein R1 is Y-2B, R2 is H, R9 is CHs and R10 is H.

Table 612. Formula 1.14 wherein R1 is Y-2B, R2 is H, R9 is CHs and R10 is CH3. Table 613. Formula 1.14 wherein R1 is Y-3A, R2 is H, R9 is H and R10 is H.

Table 614. Formula 1.14 wherein R1 is Y-3A, R2 is H, R9 is CHs and R10 is H.

Table 615. Formula 1.14 wherein R1 is Y-3A, R2 is H, R9 is CHs and R10 is CH3. Table 616. Formula 1.14 wherein R1 is Y-3B, R2 is H, R9 is H and R10 is H.

Table 617. Formula 1.14 wherein R1 is Y-3B, R2 is H, R9 is CHs and R10 is H.

Table 618. Formula 1.14 wherein R1 is Y-3B, R2 is H, R9 is CHs and R10 is CH3. Table 619. Formula 1.14 wherein R1 is Y-3C, R2 is H, R9 is H and R10 is H.

Table 620. Formula 1.14 wherein R1 is Y-3C, R2 is H, R9 is CH3 and R10 is H.

Table 621 . Formula 1.14 wherein R1 is Y-3C, R2 is H, R9 is CH3 and R10 is CH3.

Table 622. Formula 1.14 wherein R1 is Y-3D, R2 is H, R9 is H and R10 is H. Table 623. Formula 1.14 wherein R1 is Y-3D, R2 is H, R9 is CH3 and R10 is H.

Table 624. Formula 1.14 wherein R1 is Y-3D, R2 is H, R9 is CH3 and R10 is CH3.

Table 625. Formula 1.14 wherein R1 is Y-4A, R2 is H, R9 is H and R10 is H. Table 626. Formula 1.14 wherein R1 is Y-4A, R2 is H, R9 is CH3 and R10 is H.

Table 627. Formula 1.14 wherein R1 is Y-4A, R2 is H, R9 is CH3 and R10 is CH3.

Table 628. Formula 1.14 wherein R1 is Y-4B, R2 is H, R9 is H and R10 is H. Table 629. Formula 1.14 wherein R1 is Y-4B, R2 is H, R9 is CH3 and R10 is H.

Table 630. Formula 1.14 wherein R1 is Y-4B, R2 is H, R9 is CH3 and R10 is CH3.

Table 631 . Formula 1.14 wherein R1 is Y-4C, R2 is H, R9 is H and R10 is H. Table 632. Formula 1.14 wherein R1 is Y-4C, R2 is H, R9 is CH3 and R10 is H.

Table 633. Formula 1.14 wherein R1 is Y-4C, R2 is H, R9 is CH3 and R10 is CH3.

Table 634. Formula 1.14 wherein R1 is Y-4D, R2 is H, R9 is H and R10 is H. Table 635. Formula 1.14 wherein R1 is Y-4D, R2 is H, R9 is CH3 and R10 is H.

Table 636. Formula 1.14 wherein R1 is Y-4D, R2 is H, R9 is CH3 and R10 is CH3.

Table 637. Formula 1.14 wherein R1 is Y-5A, R2 is H, R9 is H and R10 is H. Table 638. Formula 1.14 wherein R1 is Y-5A, R2 is H, R9 is CH3 and R10 is H.

Table 639. Formula 1.14 wherein R1 is Y-5A, R2 is H, R9 is CH3 and R10 is CH3.

Table 640. Formula 1.14 wherein R1 is Y-5B, R2 is H, R9 is H and R10 is H. Table 641 . Formula 1.14 wherein R1 is Y-5B, R2 is H, R9 is CH3 and R10 is H.

Table 642. Formula 1.14 wherein R1 is Y-5B, R2 is H, R9 is CH3 and R10 is CH3.

Table 643. Formula 1.14 wherein R1 is Y-6A, R2 is H, R9 is H and R10 is H. Table 644. Formula 1.14 wherein R1 is Y-6A, R2 is H, R9 is CH3 and R10 is H.

Table 645. Formula 1.14 wherein R1 is Y-6A, R2 is H, R9 is CH3 and R10 is CH3.

Table 646. Formula 1.14 wherein R1 is Y-6B, R2 is H, R9 is H and R10 is H. Table 647. Formula 1.14 wherein R1 is Y-6B, R2 is H, R9 is CH3 and R10 is H.

Table 648. Formula 1.14 wherein R1 is Y-6B, R2 is H, R9 is CH3 and R10 is CH3.

Table 649. Formula 1.14 wherein R1 is Y-7A, R2 is H, R9 is H and R10 is H. Table 650. Formula 1.14 wherein R1 is Y-7A, R2 is H, R9 is CH3 and R10 is H.

Table 651 . Formula 1.14 wherein R1 is Y-7A, R2 is H, R9 is CH3 and R10 is CH3.

Table 652. Formula 1.14 wherein R1 is Y-7B, R2 is H, R9 is H and R10 is H. Table 653. Formula 1.14 wherein R1 is Y-7B, R2 is H, R9 is CH3 and R10 is H.

Table 654. Formula 1.14 wherein R1 is Y-7B, R2 is H, R9 is CH3 and R10 is CH3.

Table 655. Formula 1.14 wherein R1 is Y-8A, R2 is H, R9 is H and R10 is H.

Table 656. Formula 1.14 wherein R1 is Y-8A, R2 is H, R9 is CH3 and R10 is H.

Table 657. Formula 1.14 wherein R1 is Y-8A, R2 is H, R9 is CH3 and R10 is CH3.

Table 658. Formula 1.14 wherein R1 is Y-8B, R2 is H, R9 is H and R10 is H.

Table 659. Formula 1.14 wherein R1 is Y-8B, R2 is H, R9 is CH3 and R10 is H.

Table 660. Formula 1.14 wherein R1 is Y-8B, R2 is H, R9 is CH3 and R10 is CH3.

Table 661 . Formula 1.14 wherein R1 is Y-1A, R2 is CH3, R9 is H and R10 is H. Table 662. Formula 1.14 wherein R1 is Y-1A, R2 is CH3, R9 is CH3 and R10 is H. Table 663. Formula 1.14 wherein R1 is Y-1A, R2 is CH3, R9 is CH3 and R10 is CH3. Table 664. Formula 1.14 wherein R1 is Y-1 B, R2 is CH3, R9 is H and R10 is H. Table 665. Formula 1.14 wherein R1 is Y-1 B, R2 is CH3, R9 is CH3 and R10 is H. Table 666. Formula 1.14 wherein R1 is Y-1 B, R2 is CH3, R9 is CH3 and R10 is CH3. Table 667. Formula 1.14 wherein R1 is Y-2A, R2 is CH3, R9 is H and R10 is H. Table 668. Formula 1.14 wherein R1 is Y-2A, R2 is CH3, R9 is CH3 and R10 is H. Table 669. Formula 1.14 wherein R1 is Y-2A, R2 is CH3, R9 is CH3 and R10 is CH3. Table 670. Formula 1.14 wherein R1 is Y-2B, R2 is CH3, R9 is H and R10 is H. Table 671 . Formula 1.14 wherein R1 is Y-2B, R2 is CH3, R9 is CH3 and R10 is H. Table 672. Formula 1.14 wherein R1 is Y-2B, R2 is CH3, R9 is CH3 and R10 is CH3. Table 673. Formula 1.14 wherein R1 is Y-3A, R2 is CH3, R9 is H and R10 is H. Table 674. Formula 1.14 wherein R1 is Y-3A, R2 is CH3, R9 is CH3 and R10 is H. Table 675. Formula 1.14 wherein R1 is Y-3A, R2 is CH3, R9 is CH3 and R10 is CH3. Table 676. Formula 1.14 wherein R1 is Y-3B, R2 is CH3, R9 is H and R10 is H. Table 677. Formula 1.14 wherein R1 is Y-3B, R2 is CH3, R9 is CH3 and R10 is H. Table 678. Formula 1.14 wherein R1 is Y-3B, R2 is CH3, R9 is CH3 and R10 is CH3. Table 679. Formula 1.14 wherein R1 is Y-3C, R2 is CH3, R9 is H and R10 is H. Table 680. Formula 1.14 wherein R1 is Y-3C, R2 is CH3, R9 is CH3 and R10 is H. Table 681 . Formula 1.14 wherein R1 is Y-3C, R2 is CH3, R9 is CH3 and R10 is CH3. Table 682. Formula 1.14 wherein R1 is Y-3D, R2 is CH3, R9 is H and R10 is H. Table 683. Formula 1.14 wherein R1 is Y-3D, R2 is CH3, R9 is CH3 and R10 is H. Table 684. Formula 1.14 wherein R1 is Y-3D, R2 is CH3, R9 is CH3 and R10 is CH3. Table 685. Formula 1.14 wherein R1 is Y-4A, R2 is CH3, R9 is H and R10 is H. Table 686. Formula 1.14 wherein R1 is Y-4A, R2 is CH3, R9 is CH3 and R10 is H. Table 687. Formula 1.14 wherein R1 is Y-4A, R2 is CH3, R9 is CH3 and R10 is CH3. Table 688. Formula 1.14 wherein R1 is Y-4B, R2 is CH3, R9 is H and R10 is H. Table 689. Formula 1.14 wherein R1 is Y-4B, R2 is CH3, R9 is CH3 and R10 is H. Table 690. Formula 1.14 wherein R1 is Y-4B, R2 is CH3, R9 is CH3 and R10 is CH3. Table 691 . Formula 1.14 wherein R1 is Y-4C, R2 is CH3, R9 is H and R10 is H.

Table 692. Formula 1.14 wherein R1 is Y-4C, R2 is CH3, R9 is CH3 and R10 is H.

Table 693. Formula 1.14 wherein R1 is Y-4C, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 694. Formula 1.14 wherein R1 is Y-4D, R2 is CH3, R9 is H and R10 is H. Table 695. Formula 1.14 wherein R1 is Y-4D, R2 is CH3, R9 is CH3 and R10 is H.

Table 696. Formula 1.14 wherein R1 is Y-4D, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 697. Formula 1.14 wherein R1 is Y-5A, R2 is CH3, R9 is H and R10 is H.

Table 698. Formula 1.14 wherein R1 is Y-5A, R2 is CH3, R9 is CH3 and R10 is H.

Table 699. Formula 1.14 wherein R1 is Y-5A, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 700. Formula 1.14 wherein R1 is Y-5B, R2 is CH3, R9 is H and R10 is H.

Table 701 . Formula 1.14 wherein R1 is Y-5B, R2 is CH3, R9 is CH3 and R10 is H.

Table 702. Formula 1.14 wherein R1 is Y-5B, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 703. Formula 1.14 wherein R1 is Y-6A, R2 is CH3, R9 is H and R10 is H.

Table 704. Formula 1.14 wherein R1 is Y-6A, R2 is CH3, R9 is CH3 and R10 is H.

Table 705. Formula 1.14 wherein R1 is Y-6A, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 706. Formula 1.14 wherein R1 is Y-6B, R2 is CH3, R9 is H and R10 is H.

Table 707. Formula 1.14 wherein R1 is Y-6B, R2 is CH3, R9 is CH3 and R10 is H.

Table 708. Formula 1.14 wherein R1 is Y-6B, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 709. Formula 1.14 wherein R1 is Y-7A, R2 is CH3, R9 is H and R10 is H.

Table 710. Formula 1.14 wherein R1 is Y-7A, R2 is CH3, R9 is CH3 and R10 is H.

Table 71 1 . Formula 1.14 wherein R1 is Y-7A, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 712. Formula 1.14 wherein R1 is Y-7B, R2 is CH3, R9 is H and R10 is H.

Table 713. Formula 1.14 wherein R1 is Y-7B, R2 is CH3, R9 is CH3 and R10 is H.

Table 714. Formula 1.14 wherein R1 is Y-7B, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 715. Formula 1.14 wherein R1 is Y-8A, R2 is CH3, R9 is H and R10 is H.

Table 716. Formula 1.14 wherein R1 is Y-8A, R2 is CH3, R9 is CH3 and R10 is H.

Table 717. Formula 1.14 wherein R1 is Y-8A, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 718. Formula 1.14 wherein R1 is Y-8B, R2 is CH3, R9 is H and R10 is H.

Table 719. Formula 1.14 wherein R1 is Y-8B, R2 is CH3, R9 is CH3 and R10 is H.

Table 720. Formula 1.14 wherein R1 is Y-8B, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 721 . Formula 1.14 wherein R1 is Y-1A, R2 is C2H5, R9 is H and R10 is H. Table 722. Formula 1.14 wherein R1 is Y-1A, R2 is C2H5, R9 is CH3 and R10 is H.

Table 723. Formula 1.14 wherein R1 is Y-1A, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 724. Formula 1.14 wherein R1 is Y-1 B, R2 is C2H5, R9 is H and R10 is H. Table 725. Formula 1.14 wherein R1 is Y-1 B, R2 is C2H5, R9 is CH3 and R10 is H.

Table 726. Formula 1.14 wherein R1 is Y-1 B, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 727. Formula 1.14 wherein R1 is Y-2A, R2 is C2H5, R9 is H and R10 is H.

Table 728. Formula 1.14 wherein R1 is Y-2A, R2 is C2H5, R9 is CH3 and R10 is H.

Table 729. Formula 1.14 wherein R1 is Y-2A, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 730. Formula 1.14 wherein R1 is Y-2B, R2 is C2H5, R9 is H and R10 is H. Table 731 . Formula 1.14 wherein R1 is Y-2B, R2 is C2H5, R9 is CH3 and R10 is H.

Table 732. Formula 1.14 wherein R1 is Y-2B, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 733. Formula 1.14 wherein R1 is Y-3A, R2 is C2H5, R9 is H and R10 is H. Table 734. Formula 1.14 wherein R1 is Y-3A, R2 is C2H5, R9 is CH3 and R10 is H.

Table 735. Formula 1.14 wherein R1 is Y-3A, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 736. Formula 1.14 wherein R1 is Y-3B, R2 is C2H5, R9 is H and R10 is H. Table 737. Formula 1.14 wherein R1 is Y-3B, R2 is C2H5, R9 is CH3 and R10 is H.

Table 738. Formula 1.14 wherein R1 is Y-3B, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 739. Formula 1.14 wherein R1 is Y-3C, R2 is C2H5, R9 is H and R10 is H. Table 740. Formula 1.14 wherein R1 is Y-3C, R2 is C2H5, R9 is CH3 and R10 is H.

Table 741 . Formula 1.14 wherein R1 is Y-3C, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 742. Formula 1.14 wherein R1 is Y-3D, R2 is C2H5, R9 is H and R10 is H. Table 743. Formula 1.14 wherein R1 is Y-3D, R2 is C2H5, R9 is CH3 and R10 is H.

Table 744. Formula 1.14 wherein R1 is Y-3D, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 745. Formula 1.14 wherein R1 is Y-4A, R2 is C2H5, R9 is H and R10 is H. Table 746. Formula 1.14 wherein R1 is Y-4A, R2 is C2H5, R9 is CH3 and R10 is H.

Table 747. Formula 1.14 wherein R1 is Y-4A, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 748. Formula 1.14 wherein R1 is Y-4B, R2 is C2H5, R9 is H and R10 is H. Table 749. Formula 1.14 wherein R1 is Y-4B, R2 is C2H5, R9 is CH3 and R10 is H.

Table 750. Formula 1.14 wherein R1 is Y-4B, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 751 . Formula 1.14 wherein R1 is Y-4C, R2 is C2H5, R9 is H and R10 is H. Table 752. Formula 1.14 wherein R1 is Y-4C, R2 is C2H5, R9 is CH3 and R10 is H.

Table 753. Formula 1.14 wherein R1 is Y-4C, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 754. Formula 1.14 wherein R1 is Y-4D, R2 is C2H5, R9 is H and R10 is H. Table 755. Formula 1.14 wherein R1 is Y-4D, R2 is C2H5, R9 is CH3 and R10 is H.

Table 756. Formula 1.14 wherein R1 is Y-4D, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 757. Formula 1.14 wherein R1 is Y-5A, R2 is C2H5, R9 is H and R10 is H. Table 758. Formula 1.14 wherein R1 is Y-5A, R2 is C2H5, R9 is CH3 and R10 is H.

Table 759. Formula 1.14 wherein R1 is Y-5A, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 760. Formula 1.14 wherein R1 is Y-5B, R2 is C2H5, R9 is H and R10 is H. Table 761 . Formula 1.14 wherein R1 is Y-5B, R2 is C2H5, R9 is CH3 and R10 is H.

Table 762. Formula 1.14 wherein R1 is Y-5B, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 763. Formula 1.14 wherein R1 is Y-6A, R2 is C2H5, R9 is H and R10 is H.

Table 764. Formula 1.14 wherein R1 is Y-6A, R2 is C2H5, R9 is CHs and R10 is H. Table 765. Formula 1.14 wherein R1 is Y-6A, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 766. Formula 1.14 wherein R1 is Y-6B, R2 is C2H5, R9 is H and R10 is H.

Table 767. Formula 1.14 wherein R1 is Y-6B, R2 is C2H5, R9 is CH3 and R10 is H. Table 768. Formula 1.14 wherein R1 is Y-6B, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 769. Formula 1.14 wherein R1 is Y-7A, R2 is C2H5, R9 is H and R10 is H.

Table 770. Formula 1.14 wherein R1 is Y-7A, R2 is C2H5, R9 is CH3 and R10 is H. Table 771 . Formula 1.14 wherein R1 is Y-7A, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 772. Formula 1.14 wherein R1 is Y-7B, R2 is C2H5, R9 is H and R10 is H.

Table 773. Formula 1.14 wherein R1 is Y-7B, R2 is C2H5, R9 is CH3 and R10 is H. Table 774. Formula 1.14 wherein R1 is Y-7B, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 775. Formula 1.14 wherein R1 is Y-8A, R2 is C2H5, R9 is H and R10 is H.

Table 776. Formula 1.14 wherein R1 is Y-8A, R2 is C2H5, R9 is CH3 and R10 is H. Table 777. Formula 1.14 wherein R1 is Y-8A, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 778. Formula 1.14 wherein R1 is Y-8B, R2 is C2H5, R9 is H and R10 is H.

Table 779. Formula 1.14 wherein R1 is Y-8B, R2 is C2H5, R9 is CH3 and R10 is H. Table 780. Formula 1.14 wherein R1 is Y-8B, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 781 . Formula 1.14 wherein R1 is Y-1A, R2 is C-C3H5, R9 is H and R10 is H. Table 782. Formula 1.14 wherein R1 is Y-1A, R2 is C-C3H5, R9 is CH3 and R10 is H. Table 783. Formula 1.14 wherein R1 is Y-1A, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 784. Formula 1.14 wherein R1 is Y-1 B, R2 is C-C3H5, R9 is H and R10 is H. Table 785. Formula 1.14 wherein R1 is Y-1 B, R2 is C-C3H5, R9 is CH3, R10 is H.

Table 786. Formula 1.14 wherein R1 is Y-1 B, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 787. Formula 1.14 wherein R1 is Y-2A, R2 is C-C3H5, R9 is H and R10 is H. Table 788. Formula 1.14 wherein R1 is Y-2A, R2 is C-C3H5, R9 is CH3 and R10 is H. Table 789. Formula 1.14 wherein R1 is Y-2A, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 790. Formula 1.14 wherein R1 is Y-2B, R2 is C-C3H5, R9 is H and R10 is H. Table 791 . Formula 1.14 wherein R1 is Y-2B, R2 is C-C3H5, R9 is CH3 and R10 is H. Table 792. Formula 1.14 wherein R1 is Y-2B, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 793. Formula 1.14 wherein R1 is Y-3A, R2 is C-C3H5, R9 is H and R10 is H. Table 794. Formula 1.14 wherein R1 is Y-3A, R2 is C-C3H5, R9 is CH3 and R10 is H. Table 795. Formula 1.14 wherein R1 is Y-3A, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 796. Formula 1.14 wherein R1 is Y-3B, R2 is C-C3H5, R9 is H and R10 is H. Table 797. Formula 1.14 wherein R1 is Y-3B, R2 is C-C3H5, R9 is CH3 and R10 is H. Table 798. Formula 1.14 wherein R1 is Y-3B, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 799. Formula 1.14 wherein R1 is Y-3C, R2 is C-C3H5, R9 is H and R10 is H.

Table 800. Formula 1.14 wherein R1 is Y-3C, R2 is C-C3H5, R9 is CHs and R10 is H. Table 801 . Formula 1.14 wherein R1 is Y-3C, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 802. Formula 1.14 wherein R1 is Y-3D, R2 is C-C3H5, R9 is H and R10 is H. Table 803. Formula 1.14 wherein R1 is Y-3D, R2 is C-C3H5, R9 is CHs and R10 is H. Table 804. Formula 1.14 wherein R1 is Y-3D, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 805. Formula 1.14 wherein R1 is Y-4A, R2 is C-C3H5, R9 is H and R10 is H. Table 806. Formula 1.14 wherein R1 is Y-4A, R2 is C-C3H5, R9 is CHs and R10 is H. Table 807. Formula 1.14 wherein R1 is Y-4A, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 808. Formula 1.14 wherein R1 is Y-4B, R2 is C-C3H5, R9 is H and R10 is H. Table 809. Formula 1.14 wherein R1 is Y-4B, R2 is C-C3H5, R9 is CHs and R10 is H. Table 810. Formula 1.14 wherein R1 is Y-4B, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 81 1 . Formula 1.14 wherein R1 is Y-4C, R2 is C-C3H5, R9 is H and R10 is H. Table 812. Formula 1.14 wherein R1 is Y-4C, R2 is C-C3H5, R9 is CHs and R10 is H. Table 813. Formula 1.14 wherein R1 is Y-4C, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 814. Formula 1.14 wherein R1 is Y-4D, R2 is C-C3H5, R9 is H and R10 is H. Table 815. Formula 1.14 wherein R1 is Y-4D, R2 is C-C3H5, R9 is CHs and R10 is H. Table 816. Formula 1.14 wherein R1 is Y-4D, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 817. Formula 1.14 wherein R1 is Y-5A, R2 is C-C3H5, R9 is H and R10 is H. Table 818. Formula 1.14 wherein R1 is Y-5A, R2 is C-C3H5, R9 is CHs and R10 is H. Table 819. Formula 1.14 wherein R1 is Y-5A, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 820. Formula 1.14 wherein R1 is Y-5B, R2 is C-C3H5, R9 is H and R10 is H. Table 821 . Formula 1.14 wherein R1 is Y-5B, R2 is C-C3H5, R9 is CHs and R10 is H. Table 822. Formula 1.14 wherein R1 is Y-5B, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 823. Formula 1.14 wherein R1 is Y-6A, R2 is C-C3H5, R9 is H and R10 is H. Table 824. Formula 1.14 wherein R1 is Y-6A, R2 is C-C3H5, R9 is CHs and R10 is H. Table 825. Formula 1.14 wherein R1 is Y-6A, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 826. Formula 1.14 wherein R1 is Y-6B, R2 is C-C3H5, R9 is H and R10 is H. Table 827. Formula 1.14 wherein R1 is Y-6B, R2 is C-C3H5, R9 is CHs and R10 is H. Table 828. Formula 1.14 wherein R1 is Y-6B, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 829. Formula 1.14 wherein R1 is Y-7A, R2 is C-C3H5, R9 is H and R10 is H. Table 830. Formula 1.14 wherein R1 is Y-7A, R2 is C-C3H5, R9 is CHs and R10 is H. Table 831 . Formula 1.14 wherein R1 is Y-7A, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 832. Formula 1.14 wherein R1 is Y-7B, R2 is C-C3H5, R9 is H and R10 is H. Table 833. Formula 1.14 wherein R1 is Y-7B, R2 is C-C3H5, R9 is CHs and R10 is H. Table 834. Formula 1.14 wherein R1 is Y-7B, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 835. Formula 1.14 wherein R1 is Y-8A, R2 is C-C3H5, R9 is H and R10 is H.

Table 836. Formula 1.14 wherein R1 is Y-8A, R2 is C-C3H5, R9 is CHs and R10 is H. Table 837. Formula 1.14 wherein R1 is Y-8A, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 838. Formula 1.14 wherein R1 is Y-8B, R2 is C-C3H5, R9 is H and R10 is H. Table 839. Formula 1.14 wherein R1 is Y-8B, R2 is C-C3H5, R9 is CHs and R10 is H. Table 840. Formula 1.14 wherein R1 is Y-8B, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 841 . Formula 1.17 wherein R1 is Y-1A, R2 is H, R9 is H and R10 is H.

Table 842. Formula 1.17 wherein R1 is Y-1A, R2 is H, R9 is CHs and, R10 is H.

Table 843. Formula 1.17 wherein R1 is Y-1A, R2 is H, R9 is CHs and R10 is CH3. Table 844. Formula 1.17 wherein R1 is Y-1 B, R2 is H, R9 is H and R10 is H.

Table 845. Formula 1.17 wherein R1 is Y-1 B, R2 is H, R9 is CHs and R10 is H.

Table 846. Formula 1.17 wherein R1 is Y-1 B, R2 is H, R9 is CHs and R10 is CH3. Table 847. Formula 1.17 wherein R1 is Y-2A, R2 is H, R9 is H and R10 is H.

Table 848. Formula 1.17 wherein R1 is Y-2A, R2 is H, R9 is CHs and R10 is H.

Table 849. Formula 1.17 wherein R1 is Y-2A, R2 is H, R9 is CHs and R10 is CH3. Table 850. Formula 1.17 wherein R1 is Y-2B, R2 is H, R9 is H and R10 is H.

Table 851 . Formula 1.17 wherein R1 is Y-2B, R2 is H, R9 is CHs and R10 is H.

Table 852. Formula 1.17 wherein R1 is Y-2B, R2 is H, R9 is CHs and R10 is CH3. Table 853. Formula 1.17 wherein R1 is Y-3A, R2 is H, R9 is H and R10 is H.

Table 854. Formula 1.17 wherein R1 is Y-3A, R2 is H, R9 is CHs and R10 is H.

Table 855. Formula 1.17 wherein R1 is Y-3A, R2 is H, R9 is CHs and R10 is CH3. Table 856. Formula 1.17 wherein R1 is Y-3B, R2 is H, R9 is H and R10 is H.

Table 857. Formula 1.17 wherein R1 is Y-3B, R2 is H, R9 is CHs and R10 is H.

Table 858. Formula 1.17 wherein R1 is Y-3B, R2 is H, R9 is CHs and R10 is CH3. Table 859. Formula 1.17 wherein R1 is Y-3C, R2 is H, R9 is H and R10 is H.

Table 860. Formula 1.17 wherein R1 is Y-3C, R2 is H, R9 is CHs and R10 is H.

Table 861 . Formula 1.17 wherein R1 is Y-3C, R2 is H, R9 is CHs and R10 is CH3. Table 862. Formula 1.17 wherein R1 is Y-3D, R2 is H, R9 is H and R10 is H.

Table 863. Formula 1.17 wherein R1 is Y-3D, R2 is H, R9 is CHs and R10 is H.

Table 864. Formula 1.17 wherein R1 is Y-3D, R2 is H, R9 is CHs and R10 is CH3. Table 865. Formula 1.17 wherein R1 is Y-4A, R2 is H, R9 is H and R10 is H.

Table 866. Formula 1.17 wherein R1 is Y-4A, R2 is H, R9 is CHs and R10 is H.

Table 867. Formula 1.17 wherein R1 is Y-4A, R2 is H, R9 is CHs and R10 is CH3. Table 868. Formula 1.17 wherein R1 is Y-4B, R2 is H, R9 is H and R10 is H.

Table 869. Formula 1.17 wherein R1 is Y-4B, R2 is H, R9 is CHs and R10 is H.

Table 870. Formula 1.17 wherein R1 is Y-4B, R2 is H, R9 is CHs and R10 is CH3. Table 871 . Formula 1.17 wherein R1 is Y-4C, R2 is H, R9 is H and R10 is H.

Table 872. Formula 1.17 wherein R1 is Y-4C, R2 is H, R9 is CH3 and R10 is H.

Table 873. Formula 1.17 wherein R1 is Y-4C, R2 is H, R9 is CH3 and R10 is CH3.

Table 874. Formula 1.17 wherein R1 is Y-4D, R2 is H, R9 is H and R10 is H.

Table 875. Formula 1.17 wherein R1 is Y-4D, R2 is H, R9 is CH3 and R10 is H.

Table 876. Formula 1.17 wherein R1 is Y-4D, R2 is H, R9 is CH3 and R10 is CH3.

Table 877. Formula 1.17 wherein R1 is Y-5A, R2 is H, R9 is H and R10 is H.

Table 878. Formula 1.17 wherein R1 is Y-5A, R2 is H, R9 is CH3 and R10 is H.

Table 879. Formula 1.17 wherein R1 is Y-5A, R2 is H, R9 is CH3 and R10 is CH3.

Table 880. Formula 1.17 wherein R1 is Y-5B, R2 is H, R9 is H and R10 is H.

Table 881 . Formula 1.17 wherein R1 is Y-5B, R2 is H, R9 is CH3 and R10 is H.

Table 882. Formula 1.17 wherein R1 is Y-5B, R2 is H, R9 is CH3 and R10 is CH3.

Table 883. Formula 1.17 wherein R1 is Y-6A, R2 is H, R9 is H and R10 is H.

Table 884. Formula 1.17 wherein R1 is Y-6A, R2 is H, R9 is CH3 and R10 is H.

Table 885. Formula 1.17 wherein R1 is Y-6A, R2 is H, R9 is CH3 and R10 is CH3.

Table 886. Formula 1.17 wherein R1 is Y-6B, R2 is H, R9 is H and R10 is H.

Table 887. Formula 1.17 wherein R1 is Y-6B, R2 is H, R9 is CH3 and R10 is H.

Table 888. Formula 1.17 wherein R1 is Y-6B, R2 is H, R9 is CH3 and R10 is CH3.

Table 889. Formula 1.17 wherein R1 is Y-7A, R2 is H, R9 is H and R10 is H.

Table 890. Formula 1.17 wherein R1 is Y-7A, R2 is H, R9 is CH3 and R10 is H.

Table 891 . Formula 1.17 wherein R1 is Y-7A, R2 is H, R9 is CH3 and R10 is CH3.

Table 892. Formula 1.17 wherein R1 is Y-7B, R2 is H, R9 is H and R10 is H.

Table 893. Formula 1.17 wherein R1 is Y-7B, R2 is H, R9 is CH3 and R10 is H.

Table 894. Formula 1.17 wherein R1 is Y-7B, R2 is H, R9 is CH3 and R10 is CH3.

Table 895. Formula 1.17 wherein R1 is Y-8A, R2 is H, R9 is H and R10 is H.

Table 896. Formula 1.17 wherein R1 is Y-8A, R2 is H, R9 is CH3 and R10 is H.

Table 897. Formula 1.17 wherein R1 is Y-8A, R2 is H, R9 is CH3 and R10 is CH3.

Table 898. Formula 1.17 wherein R1 is Y-8B, R2 is H, R9 is H and R10 is H.

Table 899. Formula 1.17 wherein R1 is Y-8B, R2 is H, R9 is CH3 and R10 is H.

Table 900. Formula 1.17 wherein R1 is Y-8B, R2 is H, R9 is CH3 and R10 is CH3.

Table 901 . Formula 1.17 wherein R1 is Y-1A, R2 is CH3, R9 is H and R10 is H. Table 902. Formula 1.17 wherein R1 is Y-1A, R2 is CH3, R9 is CH3 and R10 is H.

Table 903. Formula 1.17 wherein R1 is Y-1A, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 904. Formula 1.17 wherein R1 is Y-1 B, R2 is CH3, R9 is H and R10 is H. Table 905. Formula 1.17 wherein R1 is Y-1 B, R2 is CH3, R9 is CH3 and R10 is H.

Table 906. Formula 1.17 wherein R1 is Y-1 B, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 907. Formula 1.17 wherein R1 is Y-2A, R2 is CH3, R9 is H and R10 is H.

Table 908. Formula 1.17 wherein R1 is Y-2A, R2 is CH3, R9 is CH3 and R10 is H.

Table 909. Formula 1.17 wherein R1 is Y-2A, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 910. Formula 1.17 wherein R1 is Y-2B, R2 is CH3, R9 is H and R10 is H. Table 91 1 . Formula 1.17 wherein R1 is Y-2B, R2 is CH3, R9 is CH3 and R10 is H.

Table 912. Formula 1.17 wherein R1 is Y-2B, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 913. Formula 1.17 wherein R1 is Y-3A, R2 is CH3, R9 is H and R10 is H. Table 914. Formula 1.17 wherein R1 is Y-3A, R2 is CH3, R9 is CH3 and R10 is H.

Table 915. Formula 1.17 wherein R1 is Y-3A, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 916. Formula 1.17 wherein R1 is Y-3B, R2 is CH3, R9 is H and R10 is H. Table 917. Formula 1.17 wherein R1 is Y-3B, R2 is CH3, R9 is CH3 and R10 is H.

Table 918. Formula 1.17 wherein R1 is Y-3B, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 919. Formula 1.17 wherein R1 is Y-3C, R2 is CH3, R9 is H and R10 is H. Table 920. Formula 1.17 wherein R1 is Y-3C, R2 is CH3, R9 is CH3 and R10 is H.

Table 921 . Formula 1.17 wherein R1 is Y-3C, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 922. Formula 1.17 wherein R1 is Y-3D, R2 is CH3, R9 is H and R10 is H. Table 923. Formula 1.17 wherein R1 is Y-3D, R2 is CH3, R9 is CH3 and R10 is H.

Table 924. Formula 1.17 wherein R1 is Y-3D, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 925. Formula 1.17 wherein R1 is Y-4A, R2 is CH3, R9 is H and R10 is H. Table 926. Formula 1.17 wherein R1 is Y-4A, R2 is CH3, R9 is CH3 and R10 is H.

Table 927. Formula 1.17 wherein R1 is Y-4A, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 928. Formula 1.17 wherein R1 is Y-4B, R2 is CH3, R9 is H and R10 is H. Table 929. Formula 1.17 wherein R1 is Y-4B, R2 is CH3, R9 is CH3 and R10 is H.

Table 930. Formula 1.17 wherein R1 is Y-4B, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 931 . Formula 1.17 wherein R1 is Y-4C, R2 is CH3, R9 is H and R10 is H. Table 932. Formula 1.17 wherein R1 is Y-4C, R2 is CH3, R9 is CH3 and R10 is H.

Table 933. Formula 1.17 wherein R1 is Y-4C, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 934. Formula 1.17 wherein R1 is Y-4D, R2 is CH3, R9 is H and R10 is H. Table 935. Formula 1.17 wherein R1 is Y-4D, R2 is CH3, R9 is CH3 and R10 is H.

Table 936. Formula 1.17 wherein R1 is Y-4D, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 937. Formula 1.17 wherein R1 is Y-5A, R2 is CH3, R9 is H and R10 is H. Table 938. Formula 1.17 wherein R1 is Y-5A, R2 is CH3, R9 is CH3 and R10 is H.

Table 939. Formula 1.17 wherein R1 is Y-5A, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 940. Formula 1.17 wherein R1 is Y-5B, R2 is CH3, R9 is H and R10 is H. Table 941 . Formula 1.17 wherein R1 is Y-5B, R2 is CH3, R9 is CH3 and R10 is H.

Table 942. Formula 1.17 wherein R1 is Y-5B, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 943. Formula 1.17 wherein R1 is Y-6A, R2 is CH3, R9 is H and R10 is H.

Table 944. Formula 1.17 wherein R1 is Y-6A, R2 is CH3, R9 is CH3 and R10 is H.

Table 945. Formula 1.17 wherein R1 is Y-6A, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 946. Formula 1.17 wherein R1 is Y-6B, R2 is CH3, R9 is H and R10 is H.

Table 947. Formula 1.17 wherein R1 is Y-6B, R2 is CH3, R9 is CH3 and R10 is H.

Table 948. Formula 1.17 wherein R1 is Y-6B, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 949. Formula 1.17 wherein R1 is Y-7A, R2 is CH3, R9 is H and R10 is H.

Table 950. Formula 1.17 wherein R1 is Y-7A, R2 is CH3, R9 is CH3 and R10 is H.

Table 951 . Formula 1.17 wherein R1 is Y-7A, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 952. Formula 1.17 wherein R1 is Y-7B, R2 is CH3, R9 is H and R10 is H.

Table 953. Formula 1.17 wherein R1 is Y-7B, R2 is CH3, R9 is CH3 and R10 is H.

Table 954. Formula 1.17 wherein R1 is Y-7B, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 955. Formula 1.17 wherein R1 is Y-8A, R2 is CH3, R9 is H and R10 is H.

Table 956. Formula 1.17 wherein R1 is Y-8A, R2 is CH3, R9 is CH3 and R10 is H.

Table 957. Formula 1.17 wherein R1 is Y-8A, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 958. Formula 1.17 wherein R1 is Y-8B, R2 is CH3, R9 is H and R10 is H.

Table 959. Formula 1.17 wherein R1 is Y-8B, R2 is CH3, R9 is CH3 and R10 is H.

Table 960. Formula 1.17 wherein R1 is Y-8B, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 961 . Formula 1.17 wherein R1 is Y-1A, R2 is C2H5, R9 is H and R10 is H. Table 962. Formula 1.17 wherein R1 is Y-1A, R2 is C2H5, R9 is CH3 and R10 is H.

Table 963. Formula 1.17 wherein R1 is Y-1A, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 964. Formula 1.17 wherein R1 is Y-1 B, R2 is C2H5, R9 is H and R10 is H. Table 965. Formula 1.17 wherein R1 is Y-1 B, R2 is C2H5, R9 is CH3 and R10 is H.

Table 966. Formula 1.17 wherein R1 is Y-1 B, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 967. Formula 1.17 wherein R1 is Y-2A, R2 is C2H5, R9 is H and R10 is H. Table 968. Formula 1.17 wherein R1 is Y-2A, R2 is C2H5, R9 is CH3 and R10 is H.

Table 969. Formula 1.17 wherein R1 is Y-2A, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 970. Formula 1.17 wherein R1 is Y-2B, R2 is C2H5, R9 is H and R10 is H. Table 971 . Formula 1.17 wherein R1 is Y-2B, R2 is C2H5, R9 is CH3 and R10 is H.

Table 972. Formula 1.17 wherein R1 is Y-2B, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 973. Formula 1.17 wherein R1 is Y-3A, R2 is C2H5, R9 is H and R10 is H. Table 974. Formula 1.17 wherein R1 is Y-3A, R2 is C2H5, R9 is CH3 and R10 is H.

Table 975. Formula 1.17 wherein R1 is Y-3A, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 976. Formula 1.17 wherein R1 is Y-3B, R2 is C2H5, R9 is H and R10 is H. Table 977. Formula 1.17 wherein R1 is Y-3B, R2 is C2H5, R9 is CH3 and R10 is H.

Table 978. Formula 1.17 wherein R1 is Y-3B, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 979. Formula 1.17 wherein R1 is Y-3C, R2 is C2H5, R9 is H and R10 is H.

Table 980. Formula 1.17 wherein R1 is Y-3C, R2 is C2H5, R9 is CH3 and R10 is H.

Table 981 . Formula 1.17 wherein R1 is Y-3C, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 982. Formula 1.17 wherein R1 is Y-3D, R2 is C2H5, R9 is H and R10 is H.

Table 983. Formula 1.17 wherein R1 is Y-3D, R2 is C2H5, R9 is CH3 and R10 is H.

Table 984. Formula 1.17 wherein R1 is Y-3D, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 985. Formula 1.17 wherein R1 is Y-4A, R2 is C2H5, R9 is H and R10 is H.

Table 986. Formula 1.17 wherein R1 is Y-4A, R2 is C2H5, R9 is CH3 and R10 is H.

Table 987. Formula 1.17 wherein R1 is Y-4A, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 988. Formula 1.17 wherein R1 is Y-4B, R2 is C2H5, R9 is H and R10 is H.

Table 989. Formula 1.17 wherein R1 is Y-4B, R2 is C2H5, R9 is CH3 and R10 is H.

Table 990. Formula 1.17 wherein R1 is Y-4B, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 991 . Formula 1.17 wherein R1 is Y-4C, R2 is C2H5, R9 is H and R10 is H.

Table 992. Formula 1.17 wherein R1 is Y-4C, R2 is C2H5, R9 is CH3 and R10 is H.

Table 993. Formula 1.17 wherein R1 is Y-4C, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 994. Formula 1.17 wherein R1 is Y-4D, R2 is C2H5, R9 is H and R10 is H.

Table 995. Formula 1.17 wherein R1 is Y-4D, R2 is C2H5, R9 is CH3 and R10 is H.

Table 996. Formula 1.17 wherein R1 is Y-4D, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 997. Formula 1.17 wherein R1 is Y-5A, R2 is C2H5, R9 is H and R10 is H.

Table 998. Formula 1.17 wherein R1 is Y-5A, R2 is C2H5, R9 is CH3 and R10 is H.

Table 999. Formula 1.17 wherein R1 is Y-5A, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 1000. Formula 1.17 wherein R1 is Y-5B, R2 is C2H5, R9 is H and R10 is H.

Table 1001 . Formula 1.17 wherein R1 is Y-5B, R2 is C2H5, R9 is CH3 and R10 is H.

Table 1002. Formula 1.17 wherein R1 is Y-5B, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 1003. Formula 1.17 wherein R1 is Y-6A, R2 is C2H5, R9 is H and R10 is H.

Table 1004. Formula 1.17 wherein R1 is Y-6A, R2 is C2H5, R9 is CH3 and R10 is H.

Table 1005. Formula 1.17 wherein R1 is Y-6A, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 1006. Formula 1.17 wherein R1 is Y-6B, R2 is C2H5, R9 is H and R10 is H.

Table 1007. Formula 1.17 wherein R1 is Y-6B, R2 is C2H5, R9 is CH3 and R10 is H.

Table 1008. Formula 1.17 wherein R1 is Y-6B, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 1009. Formula 1.17 wherein R1 is Y-7A, R2 is C2H5, R9 is H and R10 is H.

Table 1010. Formula 1.17 wherein R1 is Y-7A, R2 is C2H5, R9 is CH3 and R10 is H.

Table 101 1 . Formula 1.17 wherein R1 is Y-7A, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 1012. Formula 1.17 wherein R1 is Y-7B, R2 is C2H5, R9 is H and R10 is H.

Table 1013. Formula 1.17 wherein R1 is Y-7B, R2 is C2H5, R9 is CH3 and R10 is H.

Table 1014. Formula 1.17 wherein R1 is Y-7B, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 1015. Formula 1.17 wherein R1 is Y-8A, R2 is C2H5, R9 is H and R10 is H.

Table 1016. Formula 1.17 wherein R1 is Y-8A, R2 is C2H5, R9 is CHs and R10 is H. Table 1017. Formula 1.17 wherein R1 is Y-8A, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1018. Formula 1.17 wherein R1 is Y-8B, R2 is C2H5, R9 is H and R10 is H.

Table 1019. Formula 1.17 wherein R1 is Y-8B, R2 is C2H5, R9 is CH3 and R10 is H. Table 1020. Formula 1.17 wherein R1 is Y-8B, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1021 . Formula 1.17 wherein R1 is Y-1A, R2 is C-C3H5, R9 is H and R10 is H. Table 1022. Formula 1.17 wherein R1 is Y-1A, R2 is C-C3H5, R9 is CH3 and R10 is H. Table 1023. Formula 1.17 wherein R1 is Y-1A, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 1024. Formula 1.17 wherein R1 is Y-1 B, R2 is C-C3H5, R9 is H and R10 is H. Table 1025. Formula 1.17 wherein R1 is Y-1 B, R2 is C-C3H5, R9 is CH3, R10 is H.

Table 1026. Formula 1.17 wherein R1 is Y-1 B, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 1027. Formula 1.17 wherein R1 is Y-2A, R2 is C-C3H5, R9 is H and R10 is H. Table 1028. Formula 1.17 wherein R1 is Y-2A, R2 is C-C3H5, R9 is CH3 and R10 is H. Table 1029. Formula 1.17 wherein R1 is Y-2A, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 1030. Formula 1.17 wherein R1 is Y-2B, R2 is C-C3H5, R9 is H and R10 is H. Table 1031 . Formula 1.17 wherein R1 is Y-2B, R2 is C-C3H5, R9 is CH3 and R10 is H. Table 1032. Formula 1.17 wherein R1 is Y-2B, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 1033. Formula 1.17 wherein R1 is Y-3A, R2 is C-C3H5, R9 is H and R10 is H. Table 1034. Formula 1.17 wherein R1 is Y-3A, R2 is C-C3H5, R9 is CH3 and R10 is H. Table 1035. Formula 1.17 wherein R1 is Y-3A, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 1036. Formula 1.17 wherein R1 is Y-3B, R2 is C-C3H5, R9 is H and R10 is H. Table 1037. Formula 1.17 wherein R1 is Y-3B, R2 is C-C3H5, R9 is CH3 and R10 is H. Table 1038. Formula 1.17 wherein R1 is Y-3B, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 1039. Formula 1.17 wherein R1 is Y-3C, R2 is C-C3H5, R9 is H and R10 is H. Table 1040. Formula 1.17 wherein R1 is Y-3C, R2 is C-C3H5, R9 is CH3 and R10 is H. Table 1041 . Formula 1.17 wherein R1 is Y-3C, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 1042. Formula 1.17 wherein R1 is Y-3D, R2 is C-C3H5, R9 is H and R10 is H. Table 1043. Formula 1.17 wherein R1 is Y-3D, R2 is C-C3H5, R9 is CH3 and R10 is H. Table 1044. Formula 1.17 wherein R1 is Y-3D, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 1045. Formula 1.17 wherein R1 is Y-4A, R2 is C-C3H5, R9 is H and R10 is H. Table 1046. Formula 1.17 wherein R1 is Y-4A, R2 is C-C3H5, R9 is CH3 and R10 is H. Table 1047. Formula 1.17 wherein R1 is Y-4A, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 1048. Formula 1.17 wherein R1 is Y-4B, R2 is C-C3H5, R9 is H and R10 is H. Table 1049. Formula 1.17 wherein R1 is Y-4B, R2 is C-C3H5, R9 is CH3 and R10 is H. Table 1050. Formula 1.17 wherein R1 is Y-4B, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 1051 . Formula 1.17 wherein R1 is Y-4C, R2 is C-C3H5, R9 is H and R10 is H.

Table 1052. Formula 1.17 wherein R1 is Y-4C, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1053. Formula 1.17 wherein R1 is Y-4C, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1054. Formula 1.17 wherein R1 is Y-4D, R2 is C-C3H5, R9 is H and R10 is H. Table 1055. Formula 1.17 wherein R1 is Y-4D, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1056. Formula 1.17 wherein R1 is Y-4D, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1057. Formula 1.17 wherein R1 is Y-5A, R2 is C-C3H5, R9 is H and R10 is H. Table 1058. Formula 1.17 wherein R1 is Y-5A, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1059. Formula 1.17 wherein R1 is Y-5A, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1060. Formula 1.17 wherein R1 is Y-5B, R2 is C-C3H5, R9 is H and R10 is H. Table 1061 . Formula 1.17 wherein R1 is Y-5B, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1062. Formula 1.17 wherein R1 is Y-5B, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1063. Formula 1.17 wherein R1 is Y-6A, R2 is C-C3H5, R9 is H and R10 is H. Table 1064. Formula 1.17 wherein R1 is Y-6A, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1065. Formula 1.17 wherein R1 is Y-6A, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1066. Formula 1.17 wherein R1 is Y-6B, R2 is C-C3H5, R9 is H and R10 is H. Table 1067. Formula 1.17 wherein R1 is Y-6B, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1068. Formula 1.17 wherein R1 is Y-6B, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1069. Formula 1.17 wherein R1 is Y-7A, R2 is C-C3H5, R9 is H and R10 is H. Table 1070. Formula 1.17 wherein R1 is Y-7A, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1071 . Formula 1.17 wherein R1 is Y-7A, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1072. Formula 1.17 wherein R1 is Y-7B, R2 is C-C3H5, R9 is H and R10 is H. Table 1073. Formula 1.17 wherein R1 is Y-7B, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1074. Formula 1.17 wherein R1 is Y-7B, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1075. Formula 1.17 wherein R1 is Y-8A, R2 is C-C3H5, R9 is H and R10 is H. Table 1076. Formula 1.17 wherein R1 is Y-8A, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1077. Formula 1.17 wherein R1 is Y-8A, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1078. Formula 1.17 wherein R1 is Y-8B, R2 is C-C3H5, R9 is H and R10 is H. Table 1079. Formula 1.17 wherein R1 is Y-8B, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1080. Formula 1.17 wherein R1 is Y-8B, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1081 . Formula 1.18 wherein R1 is Y-1A, R2 is H, R9 is H and R10 is H.

Table 1082. Formula 1.18 wherein R1 is Y-1A, R2 is H, R9 is CHs and, R10 is H.

Table 1083. Formula 1.18 wherein R1 is Y-1A, R2 is H, R9 is CHs and R10 is CH3. Table 1084. Formula 1.18 wherein R1 is Y-1 B, R2 is H, R9 is H and R10 is H.

Table 1085. Formula 1.18 wherein R1 is Y-1 B, R2 is H, R9 is CHs and R10 is H.

Table 1086. Formula 1.18 wherein R1 is Y-1 B, R2 is H, R9 is CHs and R10 is CH3. Table 1087. Formula 1.18 wherein R1 is Y-2A, R2 is H, R9 is H and R10 is H.

Table 1088. Formula 1.18 wherein R1 is Y-2A, R2 is H, R9 is CH3 and R10 is H.

Table 1089. Formula 1.18 wherein R1 is Y-2A, R2 is H, R9 is CH3 and R10 is CH3.

Table 1090. Formula 1.18 wherein R1 is Y-2B, R2 is H, R9 is H and R10 is H. Table 1091 . Formula 1.18 wherein R1 is Y-2B, R2 is H, R9 is CH3 and R10 is H.

Table 1092. Formula 1.18 wherein R1 is Y-2B, R2 is H, R9 is CH3 and R10 is CH3.

Table 1093. Formula 1.18 wherein R1 is Y-3A, R2 is H, R9 is H and R10 is H. Table 1094. Formula 1.18 wherein R1 is Y-3A, R2 is H, R9 is CH3 and R10 is H.

Table 1095. Formula 1.18 wherein R1 is Y-3A, R2 is H, R9 is CH3 and R10 is CH3.

Table 1096. Formula 1.18 wherein R1 is Y-3B, R2 is H, R9 is H and R10 is H. Table 1097. Formula 1.18 wherein R1 is Y-3B, R2 is H, R9 is CH3 and R10 is H.

Table 1098. Formula 1.18 wherein R1 is Y-3B, R2 is H, R9 is CH3 and R10 is CH3.

Table 1099. Formula 1.18 wherein R1 is Y-3C, R2 is H, R9 is H and R10 is H. Table 1 100. Formula 1.18 wherein R1 is Y-3C, R2 is H, R9 is CH3 and R10 is H.

Table 1 101 . Formula 1.18 wherein R1 is Y-3C, R2 is H, R9 is CH3 and R10 is CH3.

Table 1 102. Formula 1.18 wherein R1 is Y-3D, R2 is H, R9 is H and R10 is H. Table 1 103. Formula 1.18 wherein R1 is Y-3D, R2 is H, R9 is CH3 and R10 is H.

Table 1 104. Formula 1.18 wherein R1 is Y-3D, R2 is H, R9 is CH3 and R10 is CH3.

Table 1 105. Formula 1.18 wherein R1 is Y-4A, R2 is H, R9 is H and R10 is H. Table 1 106. Formula 1.18 wherein R1 is Y-4A, R2 is H, R9 is CH3 and R10 is H.

Table 1 107. Formula 1.18 wherein R1 is Y-4A, R2 is H, R9 is CH3 and R10 is CH3.

Table 1 108. Formula 1.18 wherein R1 is Y-4B, R2 is H, R9 is H and R10 is H. Table 1 109. Formula 1.18 wherein R1 is Y-4B, R2 is H, R9 is CH3 and R10 is H.

Table 1 1 10. Formula 1.18 wherein R1 is Y-4B, R2 is H, R9 is CH3 and R10 is CH3.

Table 1 1 1 1 . Formula 1.18 wherein R1 is Y-4C, R2 is H, R9 is H and R10 is H. Table 1 1 12. Formula 1.18 wherein R1 is Y-4C, R2 is H, R9 is CH3 and R10 is H.

Table 1 1 13. Formula 1.18 wherein R1 is Y-4C, R2 is H, R9 is CH3 and R10 is CH3.

Table 1 1 14. Formula 1.18 wherein R1 is Y-4D, R2 is H, R9 is H and R10 is H. Table 1 1 15. Formula 1.18 wherein R1 is Y-4D, R2 is H, R9 is CH3 and R10 is H.

Table 1 1 16. Formula 1.18 wherein R1 is Y-4D, R2 is H, R9 is CH3 and R10 is CH3.

Table 1 1 17. Formula 1.18 wherein R1 is Y-5A, R2 is H, R9 is H and R10 is H. Table 1 1 18. Formula 1.18 wherein R1 is Y-5A, R2 is H, R9 is CH3 and R10 is H.

Table 1 1 19. Formula 1.18 wherein R1 is Y-5A, R2 is H, R9 is CH3 and R10 is CH3.

Table 1 120. Formula 1.18 wherein R1 is Y-5B, R2 is H, R9 is H and R10 is H. Table 1 121 . Formula 1.18 wherein R1 is Y-5B, R2 is H, R9 is CH3 and R10 is H.

Table 1 122. Formula 1.18 wherein R1 is Y-5B, R2 is H, R9 is CH3 and R10 is CH3.

Table 1 123. Formula 1.18 wherein R1 is Y-6A, R2 is H, R9 is H and R10 is H.

Table 1 124. Formula 1.18 wherein R1 is Y-6A, R2 is H, R9 is CH3 and R10 is H.

Table 1 125. Formula 1.18 wherein R1 is Y-6A, R2 is H, R9 is CH3 and R10 is CH3.

Table 1 126. Formula 1.18 wherein R1 is Y-6B, R2 is H, R9 is H and R10 is H.

Table 1 127. Formula 1.18 wherein R1 is Y-6B, R2 is H, R9 is CH3 and R10 is H.

Table 1 128. Formula 1.18 wherein R1 is Y-6B, R2 is H, R9 is CH3 and R10 is CH3.

Table 1 129. Formula 1.18 wherein R1 is Y-7A, R2 is H, R9 is H and R10 is H.

Table 1 130. Formula 1.18 wherein R1 is Y-7A, R2 is H, R9 is CH3 and R10 is H.

Table 1 131 . Formula 1.18 wherein R1 is Y-7A, R2 is H, R9 is CH3 and R10 is CH3.

Table 1 132. Formula 1.18 wherein R1 is Y-7B, R2 is H, R9 is H and R10 is H.

Table 1 133. Formula 1.18 wherein R1 is Y-7B, R2 is H, R9 is CH3 and R10 is H.

Table 1 134. Formula 1.18 wherein R1 is Y-7B, R2 is H, R9 is CH3 and R10 is CH3.

Table 1 135. Formula 1.18 wherein R1 is Y-8A, R2 is H, R9 is H and R10 is H.

Table 1 136. Formula 1.18 wherein R1 is Y-8A, R2 is H, R9 is CH3 and R10 is H.

Table 1 137. Formula 1.18 wherein R1 is Y-8A, R2 is H, R9 is CH3 and R10 is CH3.

Table 1 138. Formula 1.18 wherein R1 is Y-8B, R2 is H, R9 is H and R10 is H.

Table 1 139. Formula 1.18 wherein R1 is Y-8B, R2 is H, R9 is CH3 and R10 is H.

Table 1 140. Formula 1.18 wherein R1 is Y-8B, R2 is H, R9 is CH3 and R10 is CH3.

Table 1 141 . Formula 1.18 wherein R1 is Y-1A, R2 is CH3, R9 is H and R10 is H. Table 1 142. Formula 1.18 wherein R1 is Y-1A, R2 is CH3, R9 is CH3 and R10 is H.

Table 1 143. Formula 1.18 wherein R1 is Y-1A, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 1 144. Formula 1.18 wherein R1 is Y-1 B, R2 is CH3, R9 is H and R10 is H. Table 1 145. Formula 1.18 wherein R1 is Y-1 B, R2 is CH3, R9 is CH3 and R10 is H.

Table 1 146. Formula 1.18 wherein R1 is Y-1 B, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 1 147. Formula 1.18 wherein R1 is Y-2A, R2 is CH3, R9 is H and R10 is H. Table 1 148. Formula 1.18 wherein R1 is Y-2A, R2 is CH3, R9 is CH3 and R10 is H.

Table 1 149. Formula 1.18 wherein R1 is Y-2A, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 1 150. Formula 1.18 wherein R1 is Y-2B, R2 is CH3, R9 is H and R10 is H. Table 1 151 . Formula 1.18 wherein R1 is Y-2B, R2 is CH3, R9 is CH3 and R10 is H.

Table 1 152. Formula 1.18 wherein R1 is Y-2B, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 1 153. Formula 1.18 wherein R1 is Y-3A, R2 is CH3, R9 is H and R10 is H. Table 1 154. Formula 1.18 wherein R1 is Y-3A, R2 is CH3, R9 is CH3 and R10 is H.

Table 1 155. Formula 1.18 wherein R1 is Y-3A, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 1 156. Formula 1.18 wherein R1 is Y-3B, R2 is CH3, R9 is H and R10 is H. Table 1 157. Formula 1.18 wherein R1 is Y-3B, R2 is CH3, R9 is CH3 and R10 is H.

Table 1 158. Formula 1.18 wherein R1 is Y-3B, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 1 159. Formula 1.18 wherein R1 is Y-3C, R2 is CH3, R9 is H and R10 is H.

Table 1 160. Formula 1.18 wherein R1 is Y-3C, R2 is CH3, R9 is CH3 and R10 is H. Table 1 161 . Formula 1.18 wherein R1 is Y-3C, R2 is CHs, R9 is CH3 and R10 is CH3. Table 1 162. Formula 1.18 wherein R1 is Y-3D, R2 is CHs, R9 is H and R10 is H. Table 1 163. Formula 1.18 wherein R1 is Y-3D, R2 is CHs, R9 is CH3 and R10 is H. Table 1 164. Formula 1.18 wherein R1 is Y-3D, R2 is CHs, R9 is CH3 and R10 is CH3. Table 1 165. Formula 1.18 wherein R1 is Y-4A, R2 is CHs, R9 is H and R10 is H. Table 1 166. Formula 1.18 wherein R1 is Y-4A, R2 is CHs, R9 is CH3 and R10 is H. Table 1 167. Formula 1.18 wherein R1 is Y-4A, R2 is CHs, R9 is CHs and R10 is CH3. Table 1 168. Formula 1.18 wherein R1 is Y-4B, R2 is CHs, R9 is H and R10 is H. Table 1 169. Formula 1.18 wherein R1 is Y-4B, R2 is CHs, R9 is CH3 and R10 is H. Table 1 170. Formula 1.18 wherein R1 is Y-4B, R2 is CHs, R9 is CHs and R10 is CH3. Table 1 171 . Formula 1.18 wherein R1 is Y-4C, R2 is CHs, R9 is H and R10 is H. Table 1 172. Formula 1.18 wherein R1 is Y-4C, R2 is CHs, R9 is CH3 and R10 is H. Table 1 173. Formula 1.18 wherein R1 is Y-4C, R2 is CHs, R9 is CHs and R10 is CH3. Table 1 174. Formula 1.18 wherein R1 is Y-4D, R2 is CHs, R9 is H and R10 is H. Table 1 175. Formula 1.18 wherein R1 is Y-4D, R2 is CHs, R9 is CH3 and R10 is H. Table 1 176. Formula 1.18 wherein R1 is Y-4D, R2 is CHs, R9 is CHs and R10 is CH3. Table 1 177. Formula 1.18 wherein R1 is Y-5A, R2 is CHs, R9 is H and R10 is H. Table 1 178. Formula 1.18 wherein R1 is Y-5A, R2 is CHs, R9 is CH3 and R10 is H. Table 1 179. Formula 1.18 wherein R1 is Y-5A, R2 is CHs, R9 is CHs and R10 is CH3. Table 1 180. Formula 1.18 wherein R1 is Y-5B, R2 is CHs, R9 is H and R10 is H. Table 1 181 . Formula 1.18 wherein R1 is Y-5B, R2 is CHs, R9 is CH3 and R10 is H. Table 1 182. Formula 1.18 wherein R1 is Y-5B, R2 is CHs, R9 is CHs and R10 is CH3. Table 1 183. Formula 1.18 wherein R1 is Y-6A, R2 is CHs, R9 is H and R10 is H. Table 1 184. Formula 1.18 wherein R1 is Y-6A, R2 is CHs, R9 is CH3 and R10 is H. Table 1 185. Formula 1.18 wherein R1 is Y-6A, R2 is CHs, R9 is CHs and R10 is CH3. Table 1 186. Formula 1.18 wherein R1 is Y-6B, R2 is CHs, R9 is H and R10 is H. Table 1 187. Formula 1.18 wherein R1 is Y-6B, R2 is CHs, R9 is CH3 and R10 is H. Table 1 188. Formula 1.18 wherein R1 is Y-6B, R2 is CHs, R9 is CHs and R10 is CH3. Table 1 189. Formula 1.18 wherein R1 is Y-7A, R2 is CHs, R9 is H and R10 is H. Table 1 190. Formula 1.18 wherein R1 is Y-7A, R2 is CHs, R9 is CH3 and R10 is H. Table 1 191 . Formula 1.18 wherein R1 is Y-7A, R2 is CHs, R9 is CHs and R10 is CH3. Table 1 192. Formula 1.18 wherein R1 is Y-7B, R2 is CHs, R9 is H and R10 is H. Table 1 193. Formula 1.18 wherein R1 is Y-7B, R2 is CHs, R9 is CH3 and R10 is H. Table 1 194. Formula 1.18 wherein R1 is Y-7B, R2 is CHs, R9 is CHs and R10 is CH3. Table 1 195. Formula 1.18 wherein R1 is Y-8A, R2 is CHs, R9 is H and R10 is H.

Table 1 196. Formula 1.18 wherein R1 is Y-8A, R2 is CH3, R9 is CH3 and R10 is H. Table 1 197. Formula 1.18 wherein R1 is Y-8A, R2 is CHs, R9 is CH3 and R10 is CH3. Table 1 198. Formula 1.18 wherein R1 is Y-8B, R2 is CHs, R9 is H and R10 is H. Table 1 199. Formula 1.18 wherein R1 is Y-8B, R2 is CHs, R9 is CH3 and R10 is H. Table 1200. Formula 1.18 wherein R1 is Y-8B, R2 is CHs, R9 is CH3 and R10 is CH3. Table 1201 . Formula 1.18 wherein R1 is Y-1A, R2 is C2H5, R9 is H and R10 is H. Table 1202. Formula 1.18 wherein R1 is Y-1A, R2 is C2H5, R9 is CHs and R10 is H. Table 1203. Formula 1.18 wherein R1 is Y-1A, R2 is C2H5, R9 is CHs and R10 is CH3. Table 1204. Formula 1.18 wherein R1 is Y-1 B, R2 is C2H5, R9 is H and R10 is H. Table 1205. Formula 1.18 wherein R1 is Y-1 B, R2 is C2H5, R9 is CHs and R10 is H. Table 1206. Formula 1.18 wherein R1 is Y-1 B, R2 is C2H5, R9 is CHs and R10 is CH3. Table 1207. Formula 1.18 wherein R1 is Y-2A, R2 is C2H5, R9 is H and R10 is H. Table 1208. Formula 1.18 wherein R1 is Y-2A, R2 is C2H5, R9 is CHs and R10 is H. Table 1209. Formula 1.18 wherein R1 is Y-2A, R2 is C2H5, R9 is CHs and R10 is CH3. Table 1210. Formula 1.18 wherein R1 is Y-2B, R2 is C2H5, R9 is H and R10 is H. Table 121 1 . Formula 1.18 wherein R1 is Y-2B, R2 is C2H5, R9 is CHs and R10 is H. Table 1212. Formula 1.18 wherein R1 is Y-2B, R2 is C2H5, R9 is CHs and R10 is CH3. Table 1213. Formula 1.18 wherein R1 is Y-3A, R2 is C2H5, R9 is H and R10 is H. Table 1214. Formula 1.18 wherein R1 is Y-3A, R2 is C2H5, R9 is CHs and R10 is H. Table 1215. Formula 1.18 wherein R1 is Y-3A, R2 is C2H5, R9 is CHs and R10 is CH3. Table 1216. Formula 1.18 wherein R1 is Y-3B, R2 is C2H5, R9 is H and R10 is H. Table 1217. Formula 1.18 wherein R1 is Y-3B, R2 is C2H5, R9 is CHs and R10 is H. Table 1218. Formula 1.18 wherein R1 is Y-3B, R2 is C2H5, R9 is CHs and R10 is CH3. Table 1219. Formula 1.18 wherein R1 is Y-3C, R2 is C2H5, R9 is H and R10 is H. Table 1220. Formula 1.18 wherein R1 is Y-3C, R2 is C2H5, R9 is CHs and R10 is H. Table 1221 . Formula 1.18 wherein R1 is Y-3C, R2 is C2H5, R9 is CHs and R10 is CH3. Table 1222. Formula 1.18 wherein R1 is Y-3D, R2 is C2H5, R9 is H and R10 is H. Table 1223. Formula 1.18 wherein R1 is Y-3D, R2 is C2H5, R9 is CHs and R10 is H. Table 1224. Formula 1.18 wherein R1 is Y-3D, R2 is C2H5, R9 is CHs and R10 is CH3. Table 1225. Formula 1.18 wherein R1 is Y-4A, R2 is C2H5, R9 is H and R10 is H. Table 1226. Formula 1.18 wherein R1 is Y-4A, R2 is C2H5, R9 is CHs and R10 is H. Table 1227. Formula 1.18 wherein R1 is Y-4A, R2 is C2H5, R9 is CHs and R10 is CH3. Table 1228. Formula 1.18 wherein R1 is Y-4B, R2 is C2H5, R9 is H and R10 is H. Table 1229. Formula 1.18 wherein R1 is Y-4B, R2 is C2H5, R9 is CHs and R10 is H. Table 1230. Formula 1.18 wherein R1 is Y-4B, R2 is C2H5, R9 is CHs and R10 is CH3. Table 1231 . Formula 1.18 wherein R1 is Y-4C, R2 is C2H5, R9 is H and R10 is H.

Table 1232. Formula 1.18 wherein R1 is Y-4C, R2 is C2H5, R9 is CHs and R10 is H. Table 1233. Formula 1.18 wherein R1 is Y-4C, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1234. Formula 1.18 wherein R1 is Y-4D, R2 is C2H5, R9 is H and R10 is H.

Table 1235. Formula 1.18 wherein R1 is Y-4D, R2 is C2H5, R9 is CH3 and R10 is H. Table 1236. Formula 1.18 wherein R1 is Y-4D, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1237. Formula 1.18 wherein R1 is Y-5A, R2 is C2H5, R9 is H and R10 is H.

Table 1238. Formula 1.18 wherein R1 is Y-5A, R2 is C2H5, R9 is CH3 and R10 is H. Table 1239. Formula 1.18 wherein R1 is Y-5A, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1240. Formula 1.18 wherein R1 is Y-5B, R2 is C2H5, R9 is H and R10 is H.

Table 1241 . Formula 1.18 wherein R1 is Y-5B, R2 is C2H5, R9 is CH3 and R10 is H. Table 1242. Formula 1.18 wherein R1 is Y-5B, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1243. Formula 1.18 wherein R1 is Y-6A, R2 is C2H5, R9 is H and R10 is H.

Table 1244. Formula 1.18 wherein R1 is Y-6A, R2 is C2H5, R9 is CH3 and R10 is H. Table 1245. Formula 1.18 wherein R1 is Y-6A, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1246. Formula 1.18 wherein R1 is Y-6B, R2 is C2H5, R9 is H and R10 is H.

Table 1247. Formula 1.18 wherein R1 is Y-6B, R2 is C2H5, R9 is CH3 and R10 is H. Table 1248. Formula 1.18 wherein R1 is Y-6B, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1249. Formula 1.18 wherein R1 is Y-7A, R2 is C2H5, R9 is H and R10 is H.

Table 1250. Formula 1.18 wherein R1 is Y-7A, R2 is C2H5, R9 is CH3 and R10 is H. Table 1251 . Formula 1.18 wherein R1 is Y-7A, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1252. Formula 1.18 wherein R1 is Y-7B, R2 is C2H5, R9 is H and R10 is H.

Table 1253. Formula 1.18 wherein R1 is Y-7B, R2 is C2H5, R9 is CH3 and R10 is H. Table 1254. Formula 1.18 wherein R1 is Y-7B, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1255. Formula 1.18 wherein R1 is Y-8A, R2 is C2H5, R9 is H and R10 is H.

Table 1256. Formula 1.18 wherein R1 is Y-8A, R2 is C2H5, R9 is CH3 and R10 is H. Table 1257. Formula 1.18 wherein R1 is Y-8A, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1258. Formula 1.18 wherein R1 is Y-8B, R2 is C2H5, R9 is H and R10 is H.

Table 1259. Formula 1.18 wherein R1 is Y-8B, R2 is C2H5, R9 is CH3 and R10 is H. Table 1260. Formula 1.18 wherein R1 is Y-8B, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1261 . Formula 1.18 wherein R1 is Y-1A, R2 is C-C3H5, R9 is H and R10 is H. Table 1262. Formula 1.18 wherein R1 is Y-1A, R2 is C-C3H5, R9 is CH3 and R10 is H. Table 1263. Formula 1.18 wherein R1 is Y-1A, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 1264. Formula 1.18 wherein R1 is Y-1 B, R2 is C-C3H5, R9 is H and R10 is H. Table 1265. Formula 1.18 wherein R1 is Y-1 B, R2 is C-C3H5, R9 is CH3, R10 is H.

Table 1266. Formula 1.18 wherein R1 is Y-1 B, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 1267. Formula 1.18 wherein R1 is Y-2A, R2 is C-C3H5, R9 is H and R10 is H.

Table 1268. Formula 1.18 wherein R1 is Y-2A, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1269. Formula 1.18 wherein R1 is Y-2A, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1270. Formula 1.18 wherein R1 is Y-2B, R2 is C-C3H5, R9 is H and R10 is H. Table 1271 . Formula 1.18 wherein R1 is Y-2B, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1272. Formula 1.18 wherein R1 is Y-2B, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1273. Formula 1.18 wherein R1 is Y-3A, R2 is C-C3H5, R9 is H and R10 is H. Table 1274. Formula 1.18 wherein R1 is Y-3A, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1275. Formula 1.18 wherein R1 is Y-3A, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1276. Formula 1.18 wherein R1 is Y-3B, R2 is C-C3H5, R9 is H and R10 is H. Table 1277. Formula 1.18 wherein R1 is Y-3B, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1278. Formula 1.18 wherein R1 is Y-3B, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1279. Formula 1.18 wherein R1 is Y-3C, R2 is C-C3H5, R9 is H and R10 is H. Table 1280. Formula 1.18 wherein R1 is Y-3C, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1281 . Formula 1.18 wherein R1 is Y-3C, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1282. Formula 1.18 wherein R1 is Y-3D, R2 is C-C3H5, R9 is H and R10 is H. Table 1283. Formula 1.18 wherein R1 is Y-3D, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1284. Formula 1.18 wherein R1 is Y-3D, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1285. Formula 1.18 wherein R1 is Y-4A, R2 is C-C3H5, R9 is H and R10 is H. Table 1286. Formula 1.18 wherein R1 is Y-4A, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1287. Formula 1.18 wherein R1 is Y-4A, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1288. Formula 1.18 wherein R1 is Y-4B, R2 is C-C3H5, R9 is H and R10 is H. Table 1289. Formula 1.18 wherein R1 is Y-4B, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1290. Formula 1.18 wherein R1 is Y-4B, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1291 . Formula 1.18 wherein R1 is Y-4C, R2 is C-C3H5, R9 is H and R10 is H. Table 1292. Formula 1.18 wherein R1 is Y-4C, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1293. Formula 1.18 wherein R1 is Y-4C, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1294. Formula 1.18 wherein R1 is Y-4D, R2 is C-C3H5, R9 is H and R10 is H. Table 1295. Formula 1.18 wherein R1 is Y-4D, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1296. Formula 1.18 wherein R1 is Y-4D, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1297. Formula 1.18 wherein R1 is Y-5A, R2 is C-C3H5, R9 is H and R10 is H. Table 1298. Formula 1.18 wherein R1 is Y-5A, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1299. Formula 1.18 wherein R1 is Y-5A, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1300. Formula 1.18 wherein R1 is Y-5B, R2 is C-C3H5, R9 is H and R10 is H. Table 1301 . Formula 1.18 wherein R1 is Y-5B, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1302. Formula 1.18 wherein R1 is Y-5B, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1303. Formula 1.18 wherein R1 is Y-6A, R2 is C-C3H5, R9 is H and R10 is H.

Table 1304. Formula 1.18 wherein R1 is Y-6A, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1305. Formula 1.18 wherein R1 is Y-6A, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1306. Formula 1.18 wherein R1 is Y-6B, R2 is C-C3H5, R9 is H and R10 is H. Table 1307. Formula 1.18 wherein R1 is Y-6B, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1308. Formula 1.18 wherein R1 is Y-6B, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1309. Formula 1.18 wherein R1 is Y-7A, R2 is C-C3H5, R9 is H and R10 is H. Table 1310. Formula 1.18 wherein R1 is Y-7A, R2 is C-C3H5, R9 is CHs and R10 is H. Table 131 1 . Formula 1.18 wherein R1 is Y-7A, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1312. Formula 1.18 wherein R1 is Y-7B, R2 is C-C3H5, R9 is H and R10 is H. Table 1313. Formula 1.18 wherein R1 is Y-7B, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1314. Formula 1.18 wherein R1 is Y-7B, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1315. Formula 1.18 wherein R1 is Y-8A, R2 is C-C3H5, R9 is H and R10 is H. Table 1316. Formula 1.18 wherein R1 is Y-8A, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1317. Formula 1.18 wherein R1 is Y-8A, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1318. Formula 1.18 wherein R1 is Y-8B, R2 is C-C3H5, R9 is H and R10 is H. Table 1319. Formula 1.18 wherein R1 is Y-8B, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1320. Formula 1.18 wherein R1 is Y-8B, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1321 . Formula 1.19 wherein R1 is Y-1A, R2 is H, R9 is H and R10 is H.

Table 1322. Formula 1.19 wherein R1 is Y-1A, R2 is H, R9 is CHs and, R10 is H.

Table 1323. Formula 1.19 wherein R1 is Y-1A, R2 is H, R9 is CHs and R10 is CH3. Table 1324. Formula 1.19 wherein R1 is Y-1 B, R2 is H, R9 is H and R10 is H.

Table 1325. Formula 1.19 wherein R1 is Y-1 B, R2 is H, R9 is CHs and R10 is H.

Table 1326. Formula 1.19 wherein R1 is Y-1 B, R2 is H, R9 is CHs and R10 is CH3. Table 1327. Formula 1.19 wherein R1 is Y-2A, R2 is H, R9 is H and R10 is H.

Table 1328. Formula 1.19 wherein R1 is Y-2A, R2 is H, R9 is CHs and R10 is H.

Table 1329. Formula 1.19 wherein R1 is Y-2A, R2 is H, R9 is CHs and R10 is CH3. Table 1330. Formula 1.19 wherein R1 is Y-2B, R2 is H, R9 is H and R10 is H.

Table 1331 . Formula 1.19 wherein R1 is Y-2B, R2 is H, R9 is CHs and R10 is H.

Table 1332. Formula 1.19 wherein R1 is Y-2B, R2 is H, R9 is CHs and R10 is CH3. Table 1333. Formula 1.19 wherein R1 is Y-3A, R2 is H, R9 is H and R10 is H.

Table 1334. Formula 1.19 wherein R1 is Y-3A, R2 is H, R9 is CHs and R10 is H.

Table 1335. Formula 1.19 wherein R1 is Y-3A, R2 is H, R9 is CHs and R10 is CH3. Table 1336. Formula 1.19 wherein R1 is Y-3B, R2 is H, R9 is H and R10 is H.

Table 1337. Formula 1.19 wherein R1 is Y-3B, R2 is H, R9 is CHs and R10 is H.

Table 1338. Formula 1.19 wherein R1 is Y-3B, R2 is H, R9 is CHs and R10 is CH3. Table 1339. Formula 1.19 wherein R1 is Y-3C, R2 is H, R9 is H and R10 is H.

Table 1340. Formula 1.19 wherein R1 is Y-3C, R2 is H, R9 is CH3 and R10 is H.

Table 1341 . Formula 1.19 wherein R1 is Y-3C, R2 is H, R9 is CH3 and R10 is CH3.

Table 1342. Formula 1.19 wherein R1 is Y-3D, R2 is H, R9 is H and R10 is H. Table 1343. Formula 1.19 wherein R1 is Y-3D, R2 is H, R9 is CH3 and R10 is H.

Table 1344. Formula 1.19 wherein R1 is Y-3D, R2 is H, R9 is CH3 and R10 is CH3.

Table 1345. Formula 1.19 wherein R1 is Y-4A, R2 is H, R9 is H and R10 is H. Table 1346. Formula 1.19 wherein R1 is Y-4A, R2 is H, R9 is CH3 and R10 is H.

Table 1347. Formula 1.19 wherein R1 is Y-4A, R2 is H, R9 is CH3 and R10 is CH3.

Table 1348. Formula 1.19 wherein R1 is Y-4B, R2 is H, R9 is H and R10 is H. Table 1349. Formula 1.19 wherein R1 is Y-4B, R2 is H, R9 is CH3 and R10 is H.

Table 1350. Formula 1.19 wherein R1 is Y-4B, R2 is H, R9 is CH3 and R10 is CH3.

Table 1351 . Formula 1.19 wherein R1 is Y-4C, R2 is H, R9 is H and R10 is H. Table 1352. Formula 1.19 wherein R1 is Y-4C, R2 is H, R9 is CH3 and R10 is H.

Table 1353. Formula 1.19 wherein R1 is Y-4C, R2 is H, R9 is CH3 and R10 is CH3.

Table 1354. Formula 1.19 wherein R1 is Y-4D, R2 is H, R9 is H and R10 is H. Table 1355. Formula 1.19 wherein R1 is Y-4D, R2 is H, R9 is CH3 and R10 is H.

Table 1356. Formula 1.19 wherein R1 is Y-4D, R2 is H, R9 is CH3 and R10 is CH3.

Table 1357. Formula 1.19 wherein R1 is Y-5A, R2 is H, R9 is H and R10 is H. Table 1358. Formula 1.19 wherein R1 is Y-5A, R2 is H, R9 is CH3 and R10 is H.

Table 1359. Formula 1.19 wherein R1 is Y-5A, R2 is H, R9 is CH3 and R10 is CH3.

Table 1360. Formula 1.19 wherein R1 is Y-5B, R2 is H, R9 is H and R10 is H. Table 1361 . Formula 1.19 wherein R1 is Y-5B, R2 is H, R9 is CH3 and R10 is H.

Table 1362. Formula 1.19 wherein R1 is Y-5B, R2 is H, R9 is CH3 and R10 is CH3.

Table 1363. Formula 1.19 wherein R1 is Y-6A, R2 is H, R9 is H and R10 is H. Table 1364. Formula 1.19 wherein R1 is Y-6A, R2 is H, R9 is CH3 and R10 is H.

Table 1365. Formula 1.19 wherein R1 is Y-6A, R2 is H, R9 is CH3 and R10 is CH3.

Table 1366. Formula 1.19 wherein R1 is Y-6B, R2 is H, R9 is H and R10 is H. Table 1367. Formula 1.19 wherein R1 is Y-6B, R2 is H, R9 is CH3 and R10 is H.

Table 1368. Formula 1.19 wherein R1 is Y-6B, R2 is H, R9 is CH3 and R10 is CH3.

Table 1369. Formula 1.19 wherein R1 is Y-7A, R2 is H, R9 is H and R10 is H. Table 1370. Formula 1.19 wherein R1 is Y-7A, R2 is H, R9 is CH3 and R10 is H.

Table 1371 . Formula 1.19 wherein R1 is Y-7A, R2 is H, R9 is CH3 and R10 is CH3.

Table 1372. Formula 1.19 wherein R1 is Y-7B, R2 is H, R9 is H and R10 is H. Table 1373. Formula 1.19 wherein R1 is Y-7B, R2 is H, R9 is CH3 and R10 is H.

Table 1374. Formula 1.19 wherein R1 is Y-7B, R2 is H, R9 is CH3 and R10 is CH3.

Table 1375. Formula 1.19 wherein R1 is Y-8A, R2 is H, R9 is H and R10 is H.

Table 1376. Formula 1.19 wherein R1 is Y-8A, R2 is H, R9 is CH3 and R10 is H. Table 1377. Formula 1.19 wherein R1 is Y-8A, R2 is H, R9 is CH3 and R10 is CH3. Table 1378. Formula 1.19 wherein R1 is Y-8B, R2 is H, R9 is H and R10 is H.

Table 1379. Formula 1.19 wherein R1 is Y-8B, R2 is H, R9 is CH3 and R10 is H. Table 1380. Formula 1.19 wherein R1 is Y-8B, R2 is H, R9 is CH3 and R10 is CH3. Table 1381 . Formula 1.19 wherein R1 is Y-1A, R2 is CH3, R9 is H and R10 is H. Table 1382. Formula 1.19 wherein R1 is Y-1A, R2 is CH3, R9 is CH3 and R10 is H. Table 1383. Formula 1.19 wherein R1 is Y-1A, R2 is CH3, R9 is CH3 and R10 is CH3. Table 1384. Formula 1.19 wherein R1 is Y-1 B, R2 is CH3, R9 is H and R10 is H. Table 1385. Formula 1.19 wherein R1 is Y-1 B, R2 is CH3, R9 is CH3 and R10 is H. Table 1386. Formula 1.19 wherein R1 is Y-1 B, R2 is CH3, R9 is CH3 and R10 is CH3. Table 1387. Formula 1.19 wherein R1 is Y-2A, R2 is CH3, R9 is H and R10 is H. Table 1388. Formula 1.19 wherein R1 is Y-2A, R2 is CH3, R9 is CH3 and R10 is H.

Table 1389. Formula 1.19 wherein R1 is Y-2A, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 1390. Formula 1.19 wherein R1 is Y-2B, R2 is CH3, R9 is H and R10 is H. Table 1391 . Formula 1.19 wherein R1 is Y-2B, R2 is CH3, R9 is CH3 and R10 is H.

Table 1392. Formula 1.19 wherein R1 is Y-2B, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 1393. Formula 1.19 wherein R1 is Y-3A, R2 is CH3, R9 is H and R10 is H. Table 1394. Formula 1.19 wherein R1 is Y-3A, R2 is CH3, R9 is CH3 and R10 is H.

Table 1395. Formula 1.19 wherein R1 is Y-3A, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 1396. Formula 1.19 wherein R1 is Y-3B, R2 is CH3, R9 is H and R10 is H. Table 1397. Formula 1.19 wherein R1 is Y-3B, R2 is CH3, R9 is CH3 and R10 is H.

Table 1398. Formula 1.19 wherein R1 is Y-3B, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 1399. Formula 1.19 wherein R1 is Y-3C, R2 is CH3, R9 is H and R10 is H. Table 1400. Formula 1.19 wherein R1 is Y-3C, R2 is CH3, R9 is CH3 and R10 is H.

Table 1401 . Formula 1.19 wherein R1 is Y-3C, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 1402. Formula 1.19 wherein R1 is Y-3D, R2 is CH3, R9 is H and R10 is H. Table 1403. Formula 1.19 wherein R1 is Y-3D, R2 is CH3, R9 is CH3 and R10 is H.

Table 1404. Formula 1.19 wherein R1 is Y-3D, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 1405. Formula 1.19 wherein R1 is Y-4A, R2 is CH3, R9 is H and R10 is H. Table 1406. Formula 1.19 wherein R1 is Y-4A, R2 is CH3, R9 is CH3 and R10 is H.

Table 1407. Formula 1.19 wherein R1 is Y-4A, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 1408. Formula 1.19 wherein R1 is Y-4B, R2 is CH3, R9 is H and R10 is H. Table 1409. Formula 1.19 wherein R1 is Y-4B, R2 is CH3, R9 is CH3 and R10 is H.

Table 1410. Formula 1.19 wherein R1 is Y-4B, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 141 1 . Formula 1.19 wherein R1 is Y-4C, R2 is CH3, R9 is H and R10 is H.

Table 1412. Formula 1.19 wherein R1 is Y-4C, R2 is CH3, R9 is CH3 and R10 is H. Table 1413. Formula 1.19 wherein R1 is Y-4C, R2 is CHs, R9 is CH3 and R10 is CH3. Table 1414. Formula 1.19 wherein R1 is Y-4D, R2 is CHs, R9 is H and R10 is H. Table 1415. Formula 1.19 wherein R1 is Y-4D, R2 is CHs, R9 is CH3 and R10 is H. Table 1416. Formula 1.19 wherein R1 is Y-4D, R2 is CHs, R9 is CH3 and R10 is CH3. Table 1417. Formula 1.19 wherein R1 is Y-5A, R2 is CHs, R9 is H and R10 is H. Table 1418. Formula 1.19 wherein R1 is Y-5A, R2 is CHs, R9 is CH3 and R10 is H. Table 1419. Formula 1.19 wherein R1 is Y-5A, R2 is CHs, R9 is CHs and R10 is CH3. Table 1420. Formula 1.19 wherein R1 is Y-5B, R2 is CHs, R9 is H and R10 is H. Table 1421 . Formula 1.19 wherein R1 is Y-5B, R2 is CHs, R9 is CH3 and R10 is H. Table 1422. Formula 1.19 wherein R1 is Y-5B, R2 is CHs, R9 is CHs and R10 is CH3. Table 1423. Formula 1.19 wherein R1 is Y-6A, R2 is CHs, R9 is H and R10 is H. Table 1424. Formula 1.19 wherein R1 is Y-6A, R2 is CHs, R9 is CH3 and R10 is H. Table 1425. Formula 1.19 wherein R1 is Y-6A, R2 is CHs, R9 is CHs and R10 is CH3. Table 1426. Formula 1.19 wherein R1 is Y-6B, R2 is CHs, R9 is H and R10 is H. Table 1427. Formula 1.19 wherein R1 is Y-6B, R2 is CHs, R9 is CH3 and R10 is H. Table 1428. Formula 1.19 wherein R1 is Y-6B, R2 is CHs, R9 is CHs and R10 is CH3. Table 1429. Formula 1.19 wherein R1 is Y-7A, R2 is CHs, R9 is H and R10 is H. Table 1430. Formula 1.19 wherein R1 is Y-7A, R2 is CHs, R9 is CH3 and R10 is H. Table 1431 . Formula 1.19 wherein R1 is Y-7A, R2 is CHs, R9 is CHs and R10 is CH3. Table 1432. Formula 1.19 wherein R1 is Y-7B, R2 is CHs, R9 is H and R10 is H. Table 1433. Formula 1.19 wherein R1 is Y-7B, R2 is CHs, R9 is CH3 and R10 is H. Table 1434. Formula 1.19 wherein R1 is Y-7B, R2 is CHs, R9 is CHs and R10 is CH3. Table 1435. Formula 1.19 wherein R1 is Y-8A, R2 is CHs, R9 is H and R10 is H. Table 1436. Formula 1.19 wherein R1 is Y-8A, R2 is CHs, R9 is CH3 and R10 is H. Table 1437. Formula 1.19 wherein R1 is Y-8A, R2 is CHs, R9 is CHs and R10 is CH3. Table 1438. Formula 1.19 wherein R1 is Y-8B, R2 is CHs, R9 is H and R10 is H. Table 1439. Formula 1.19 wherein R1 is Y-8B, R2 is CHs, R9 is CH3 and R10 is H. Table 1440. Formula 1.19 wherein R1 is Y-8B, R2 is CHs, R9 is CHs and R10 is CH3. Table 1441 . Formula 1.19 wherein R1 is Y-1A, R2 is C2H5, R9 is H and R10 is H. Table 1442. Formula 1.19 wherein R1 is Y-1A, R2 is C2H5, R9 is CHs and R10 is H. Table 1443. Formula 1.19 wherein R1 is Y-1A, R2 is C2H5, R9 is CHs and R10 is CH3. Table 1444. Formula 1.19 wherein R1 is Y-1 B, R2 is C2H5, R9 is H and R10 is H. Table 1445. Formula 1.19 wherein R1 is Y-1 B, R2 is C2H5, R9 is CHs and R10 is H. Table 1446. Formula 1.19 wherein R1 is Y-1 B, R2 is C2H5, R9 is CHs and R10 is CH3. Table 1447. Formula 1.19 wherein R1 is Y-2A, R2 is C2H5, R9 is H and R10 is H.

Table 1448. Formula 1.19 wherein R1 is Y-2A, R2 is C2H5, R9 is CHs and R10 is H. Table 1449. Formula 1.19 wherein R1 is Y-2A, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1450. Formula 1.19 wherein R1 is Y-2B, R2 is C2H5, R9 is H and R10 is H. Table 1451 . Formula 1.19 wherein R1 is Y-2B, R2 is C2H5, R9 is CH3 and R10 is H. Table 1452. Formula 1.19 wherein R1 is Y-2B, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1453. Formula 1.19 wherein R1 is Y-3A, R2 is C2H5, R9 is H and R10 is H. Table 1454. Formula 1.19 wherein R1 is Y-3A, R2 is C2H5, R9 is CH3 and R10 is H. Table 1455. Formula 1.19 wherein R1 is Y-3A, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1456. Formula 1.19 wherein R1 is Y-3B, R2 is C2H5, R9 is H and R10 is H. Table 1457. Formula 1.19 wherein R1 is Y-3B, R2 is C2H5, R9 is CH3 and R10 is H. Table 1458. Formula 1.19 wherein R1 is Y-3B, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1459. Formula 1.19 wherein R1 is Y-3C, R2 is C2H5, R9 is H and R10 is H. Table 1460. Formula 1.19 wherein R1 is Y-3C, R2 is C2H5, R9 is CH3 and R10 is H. Table 1461 . Formula 1.19 wherein R1 is Y-3C, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1462. Formula 1.19 wherein R1 is Y-3D, R2 is C2H5, R9 is H and R10 is H. Table 1463. Formula 1.19 wherein R1 is Y-3D, R2 is C2H5, R9 is CH3 and R10 is H. Table 1464. Formula 1.19 wherein R1 is Y-3D, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1465. Formula 1.19 wherein R1 is Y-4A, R2 is C2H5, R9 is H and R10 is H. Table 1466. Formula 1.19 wherein R1 is Y-4A, R2 is C2H5, R9 is CH3 and R10 is H. Table 1467. Formula 1.19 wherein R1 is Y-4A, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1468. Formula 1.19 wherein R1 is Y-4B, R2 is C2H5, R9 is H and R10 is H. Table 1469. Formula 1.19 wherein R1 is Y-4B, R2 is C2H5, R9 is CH3 and R10 is H. Table 1470. Formula 1.19 wherein R1 is Y-4B, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1471 . Formula 1.19 wherein R1 is Y-4C, R2 is C2H5, R9 is H and R10 is H. Table 1472. Formula 1.19 wherein R1 is Y-4C, R2 is C2H5, R9 is CH3 and R10 is H. Table 1473. Formula 1.19 wherein R1 is Y-4C, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1474. Formula 1.19 wherein R1 is Y-4D, R2 is C2H5, R9 is H and R10 is H. Table 1475. Formula 1.19 wherein R1 is Y-4D, R2 is C2H5, R9 is CH3 and R10 is H. Table 1476. Formula 1.19 wherein R1 is Y-4D, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1477. Formula 1.19 wherein R1 is Y-5A, R2 is C2H5, R9 is H and R10 is H. Table 1478. Formula 1.19 wherein R1 is Y-5A, R2 is C2H5, R9 is CH3 and R10 is H. Table 1479. Formula 1.19 wherein R1 is Y-5A, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1480. Formula 1.19 wherein R1 is Y-5B, R2 is C2H5, R9 is H and R10 is H. Table 1481 . Formula 1.19 wherein R1 is Y-5B, R2 is C2H5, R9 is CH3 and R10 is H. Table 1482. Formula 1.19 wherein R1 is Y-5B, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1483. Formula 1.19 wherein R1 is Y-6A, R2 is C2H5, R9 is H and R10 is H.

Table 1484. Formula 1.19 wherein R1 is Y-6A, R2 is C2H5, R9 is CHs and R10 is H. Table 1485. Formula 1.19 wherein R1 is Y-6A, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1486. Formula 1.19 wherein R1 is Y-6B, R2 is C2H5, R9 is H and R10 is H.

Table 1487. Formula 1.19 wherein R1 is Y-6B, R2 is C2H5, R9 is CH3 and R10 is H. Table 1488. Formula 1.19 wherein R1 is Y-6B, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1489. Formula 1.19 wherein R1 is Y-7A, R2 is C2H5, R9 is H and R10 is H.

Table 1490. Formula 1.19 wherein R1 is Y-7A, R2 is C2H5, R9 is CH3 and R10 is H. Table 1491 . Formula 1.19 wherein R1 is Y-7A, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1492. Formula 1.19 wherein R1 is Y-7B, R2 is C2H5, R9 is H and R10 is H.

Table 1493. Formula 1.19 wherein R1 is Y-7B, R2 is C2H5, R9 is CH3 and R10 is H. Table 1494. Formula 1.19 wherein R1 is Y-7B, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1495. Formula 1.19 wherein R1 is Y-8A, R2 is C2H5, R9 is H and R10 is H.

Table 1496. Formula 1.19 wherein R1 is Y-8A, R2 is C2H5, R9 is CH3 and R10 is H. Table 1497. Formula 1.19 wherein R1 is Y-8A, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1498. Formula 1.19 wherein R1 is Y-8B, R2 is C2H5, R9 is H and R10 is H.

Table 1499. Formula 1.19 wherein R1 is Y-8B, R2 is C2H5, R9 is CH3 and R10 is H. Table 1500. Formula 1.19 wherein R1 is Y-8B, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1501 . Formula 1.19 wherein R1 is Y-1A, R2 is C-C3H5, R9 is H and R10 is H. Table 1502. Formula 1.19 wherein R1 is Y-1A, R2 is C-C3H5, R9 is CH3 and R10 is H. Table 1503. Formula 1.19 wherein R1 is Y-1A, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 1504. Formula 1.19 wherein R1 is Y-1 B, R2 is C-C3H5, R9 is H and R10 is H. Table 1505. Formula 1.19 wherein R1 is Y-1 B, R2 is C-C3H5, R9 is CH3, R10 is H.

Table 1506. Formula 1.19 wherein R1 is Y-1 B, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 1507. Formula 1.19 wherein R1 is Y-2A, R2 is C-C3H5, R9 is H and R10 is H. Table 1508. Formula 1.19 wherein R1 is Y-2A, R2 is C-C3H5, R9 is CH3 and R10 is H. Table 1509. Formula 1.19 wherein R1 is Y-2A, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 1510. Formula 1.19 wherein R1 is Y-2B, R2 is C-C3H5, R9 is H and R10 is H. Table 151 1 . Formula 1.19 wherein R1 is Y-2B, R2 is C-C3H5, R9 is CH3 and R10 is H. Table 1512. Formula 1.19 wherein R1 is Y-2B, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 1513. Formula 1.19 wherein R1 is Y-3A, R2 is C-C3H5, R9 is H and R10 is H. Table 1514. Formula 1.19 wherein R1 is Y-3A, R2 is C-C3H5, R9 is CH3 and R10 is H. Table 1515. Formula 1.19 wherein R1 is Y-3A, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 1516. Formula 1.19 wherein R1 is Y-3B, R2 is C-C3H5, R9 is H and R10 is H. Table 1517. Formula 1.19 wherein R1 is Y-3B, R2 is C-C3H5, R9 is CH3 and R10 is H. Table 1518. Formula 1.19 wherein R1 is Y-3B, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 1519. Formula 1.19 wherein R1 is Y-3C, R2 is C-C3H5, R9 is H and R10 is H.

Table 1520. Formula 1.19 wherein R1 is Y-3C, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1521 . Formula 1.19 wherein R1 is Y-3C, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1522. Formula 1.19 wherein R1 is Y-3D, R2 is C-C3H5, R9 is H and R10 is H. Table 1523. Formula 1.19 wherein R1 is Y-3D, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1524. Formula 1.19 wherein R1 is Y-3D, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1525. Formula 1.19 wherein R1 is Y-4A, R2 is C-C3H5, R9 is H and R10 is H. Table 1526. Formula 1.19 wherein R1 is Y-4A, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1527. Formula 1.19 wherein R1 is Y-4A, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1528. Formula 1.19 wherein R1 is Y-4B, R2 is C-C3H5, R9 is H and R10 is H. Table 1529. Formula 1.19 wherein R1 is Y-4B, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1530. Formula 1.19 wherein R1 is Y-4B, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1531 . Formula 1.19 wherein R1 is Y-4C, R2 is C-C3H5, R9 is H and R10 is H. Table 1532. Formula 1.19 wherein R1 is Y-4C, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1533. Formula 1.19 wherein R1 is Y-4C, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1534. Formula 1.19 wherein R1 is Y-4D, R2 is C-C3H5, R9 is H and R10 is H. Table 1535. Formula 1.19 wherein R1 is Y-4D, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1536. Formula 1.19 wherein R1 is Y-4D, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1537. Formula 1.19 wherein R1 is Y-5A, R2 is C-C3H5, R9 is H and R10 is H. Table 1538. Formula 1.19 wherein R1 is Y-5A, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1539. Formula 1.19 wherein R1 is Y-5A, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1540. Formula 1.19 wherein R1 is Y-5B, R2 is C-C3H5, R9 is H and R10 is H. Table 1541 . Formula 1.19 wherein R1 is Y-5B, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1542. Formula 1.19 wherein R1 is Y-5B, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1543. Formula 1.19 wherein R1 is Y-6A, R2 is C-C3H5, R9 is H and R10 is H. Table 1544. Formula 1.19 wherein R1 is Y-6A, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1545. Formula 1.19 wherein R1 is Y-6A, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1546. Formula 1.19 wherein R1 is Y-6B, R2 is C-C3H5, R9 is H and R10 is H. Table 1547. Formula 1.19 wherein R1 is Y-6B, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1548. Formula 1.19 wherein R1 is Y-6B, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1549. Formula 1.19 wherein R1 is Y-7A, R2 is C-C3H5, R9 is H and R10 is H. Table 1550. Formula 1.19 wherein R1 is Y-7A, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1551 . Formula 1.19 wherein R1 is Y-7A, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1552. Formula 1.19 wherein R1 is Y-7B, R2 is C-C3H5, R9 is H and R10 is H. Table 1553. Formula 1.19 wherein R1 is Y-7B, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1554. Formula 1.19 wherein R1 is Y-7B, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1555. Formula 1.19 wherein R1 is Y-8A, R2 is C-C3H5, R9 is H and R10 is H.

Table 1556. Formula 1.19 wherein R1 is Y-8A, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1557. Formula 1.19 wherein R1 is Y-8A, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1558. Formula 1.19 wherein R1 is Y-8B, R2 is C-C3H5, R9 is H and R10 is H. Table 1559. Formula 1.19 wherein R1 is Y-8B, R2 is C-C3H5, R9 is CHs and R10 is H. Table 1560. Formula 1.19 wherein R1 is Y-8B, R2 is C-C3H5, R9 is CHs and R10 is CH3. Table 1561 . Formula I.20 wherein R1 is Y-1A, R2 is H, R9 is H and R10 is H.

Table 1562. Formula I.20 wherein R1 is Y-1A, R2 is H, R9 is CHs and, R10 is H.

Table 1563. Formula I.20 wherein R1 is Y-1A, R2 is H, R9 is CHs and R10 is CH3. Table 1564. Formula I.20 wherein R1 is Y-1 B, R2 is H, R9 is H and R10 is H.

Table 1565. Formula I.20 wherein R1 is Y-1 B, R2 is H, R9 is CHs and R10 is H.

Table 1566. Formula I.20 wherein R1 is Y-1 B, R2 is H, R9 is CHs and R10 is CH3. Table 1567. Formula 1.20 wherein R1 is Y-2A, R2 is H, R9 is H and R10 is H.

Table 1568. Formula 1.20 wherein R1 is Y-2A, R2 is H, R9 is CHs and R10 is H.

Table 1569. Formula 1.20 wherein R1 is Y-2A, R2 is H, R9 is CHs and R10 is CH3. Table 1570. Formula I.20 wherein R1 is Y-2B, R2 is H, R9 is H and R10 is H.

Table 1571 . Formula 1.20 wherein R1 is Y-2B, R2 is H, R9 is CHs and R10 is H.

Table 1572. Formula 1.20 wherein R1 is Y-2B, R2 is H, R9 is CHs and R10 is CH3. Table 1573. Formula I.20 wherein R1 is Y-3A, R2 is H, R9 is H and R10 is H.

Table 1574. Formula 1.20 wherein R1 is Y-3A, R2 is H, R9 is CHs and R10 is H.

Table 1575. Formula 1.20 wherein R1 is Y-3A, R2 is H, R9 is CHs and R10 is CH3. Table 1576. Formula I.20 wherein R1 is Y-3B, R2 is H, R9 is H and R10 is H.

Table 1577. Formula I.20 wherein R1 is Y-3B, R2 is H, R9 is CHs and R10 is H.

Table 1578. Formula I.20 wherein R1 is Y-3B, R2 is H, R9 is CHs and R10 is CH3. Table 1579. Formula I.20 wherein R1 is Y-3C, R2 is H, R9 is H and R10 is H.

Table 1580. Formula I.20 wherein R1 is Y-3C, R2 is H, R9 is CHs and R10 is H.

Table 1581 . Formula I.20 wherein R1 is Y-3C, R2 is H, R9 is CHs and R10 is CH3. Table 1582. Formula I.20 wherein R1 is Y-3D, R2 is H, R9 is H and R10 is H.

Table 1583. Formula I.20 wherein R1 is Y-3D, R2 is H, R9 is CHs and R10 is H.

Table 1584. Formula I.20 wherein R1 is Y-3D, R2 is H, R9 is CHs and R10 is CH3. Table 1585. Formula 1.20 wherein R1 is Y-4A, R2 is H, R9 is H and R10 is H.

Table 1586. Formula 1.20 wherein R1 is Y-4A, R2 is H, R9 is CHs and R10 is H.

Table 1587. Formula 1.20 wherein R1 is Y-4A, R2 is H, R9 is CHs and R10 is CH3. Table 1588. Formula I.20 wherein R1 is Y-4B, R2 is H, R9 is H and R10 is H.

Table 1589. Formula I.20 wherein R1 is Y-4B, R2 is H, R9 is CHs and R10 is H.

Table 1590. Formula I.20 wherein R1 is Y-4B, R2 is H, R9 is CHs and R10 is CH3. Table 1591 . Formula I.20 wherein R1 is Y-4C, R2 is H, R9 is H and R10 is H.

Table 1592. Formula I.20 wherein R1 is Y-4C, R2 is H, R9 is CHs and R10 is H. Table 1593. Formula I.20 wherein R1 is Y-4C, R2 is H, R9 is CH3 and R10 is CH3. Table 1594. Formula I.20 wherein R1 is Y-4D, R2 is H, R9 is H and R10 is H.

Table 1595. Formula I.20 wherein R1 is Y-4D, R2 is H, R9 is CH3 and R10 is H. Table 1596. Formula I.20 wherein R1 is Y-4D, R2 is H, R9 is CH3 and R10 is CH3. Table 1597. Formula 1.20 wherein R1 is Y-5A, R2 is H, R9 is H and R10 is H.

Table 1598. Formula 1.20 wherein R1 is Y-5A, R2 is H, R9 is CH3 and R10 is H. Table 1599. Formula 1.20 wherein R1 is Y-5A, R2 is H, R9 is CH3 and R10 is CH3. Table 1600. Formula I.20 wherein R1 is Y-5B, R2 is H, R9 is H and R10 is H.

Table 1601 . Formula I.20 wherein R1 is Y-5B, R2 is H, R9 is CH3 and R10 is H. Table 1602. Formula I.20 wherein R1 is Y-5B, R2 is H, R9 is CH3 and R10 is CH3. Table 1603. Formula 1.20 wherein R1 is Y-6A, R2 is H, R9 is H and R10 is H.

Table 1604. Formula 1.20 wherein R1 is Y-6A, R2 is H, R9 is CH3 and R10 is H. Table 1605. Formula 1.20 wherein R1 is Y-6A, R2 is H, R9 is CH3 and R10 is CH3. Table 1606. Formula I.20 wherein R1 is Y-6B, R2 is H, R9 is H and R10 is H.

Table 1607. Formula I.20 wherein R1 is Y-6B, R2 is H, R9 is CH3 and R10 is H. Table 1608. Formula I.20 wherein R1 is Y-6B, R2 is H, R9 is CH3 and R10 is CH3. Table 1609. Formula I.20 wherein R1 is Y-7A, R2 is H, R9 is H and R10 is H.

Table 1610. Formula I.20 wherein R1 is Y-7A, R2 is H, R9 is CH3 and R10 is H. Table 161 1 . Formula I.20 wherein R1 is Y-7A, R2 is H, R9 is CH3 and R10 is CH3. Table 1612. Formula I.20 wherein R1 is Y-7B, R2 is H, R9 is H and R10 is H.

Table 1613. Formula I.20 wherein R1 is Y-7B, R2 is H, R9 is CH3 and R10 is H. Table 1614. Formula I.20 wherein R1 is Y-7B, R2 is H, R9 is CH3 and R10 is CH3. Table 1615. Formula I.20 wherein R1 is Y-8A, R2 is H, R9 is H and R10 is H.

Table 1616. Formula I.20 wherein R1 is Y-8A, R2 is H, R9 is CH3 and R10 is H. Table 1617. Formula I.20 wherein R1 is Y-8A, R2 is H, R9 is CH3 and R10 is CH3. Table 1618. Formula I.20 wherein R1 is Y-8B, R2 is H, R9 is H and R10 is H.

Table 1619. Formula I.20 wherein R1 is Y-8B, R2 is H, R9 is CH3 and R10 is H. Table 1620. Formula I.20 wherein R1 is Y-8B, R2 is H, R9 is CH3 and R10 is CH3. Table 1621 . Formula I.20 wherein R1 is Y-1A, R2 is CH3, R9 is H and R10 is H. Table 1622. Formula 1.20 wherein R1 is Y-1A, R2 is CH3, R9 is CH3 and R10 is H. Table 1623. Formula 1.20 wherein R1 is Y-1A, R2 is CH3, R9 is CH3 and R10 is CH3. Table 1624. Formula 1.20 wherein R1 is Y-1 B, R2 is CH3, R9 is H and R10 is H. Table 1625. Formula I.20 wherein R1 is Y-1 B, R2 is CH3, R9 is CH3 and R10 is H. Table 1626. Formula I.20 wherein R1 is Y-1 B, R2 is CH3, R9 is CH3 and R10 is CH3. Table 1627. Formula 1.20 wherein R1 is Y-2A, R2 is CH3, R9 is H and R10 is H.

Table 1628. Formula 1.20 wherein R1 is Y-2A, R2 is CH3, R9 is CH3 and R10 is H. Table 1629. Formula 1.20 wherein R1 is Y-2A, R2 is CHs, R9 is CH3 and R10 is CH3. Table 1630. Formula I.20 wherein R1 is Y-2B, R2 is CHs, R9 is H and R10 is H. Table 1631 . Formula I.20 wherein R1 is Y-2B, R2 is CHs, R9 is CH3 and R10 is H. Table 1632. Formula 1.20 wherein R1 is Y-2B, R2 is CHs, R9 is CH3 and R10 is CH3. Table 1633. Formula 1.20 wherein R1 is Y-3A, R2 is CHs, R9 is H and R10 is H. Table 1634. Formula 1.20 wherein R1 is Y-3A, R2 is CHs, R9 is CH3 and R10 is H. Table 1635. Formula 1.20 wherein R1 is Y-3A, R2 is CHs, R9 is CHs and R10 is CH3. Table 1636. Formula I.20 wherein R1 is Y-3B, R2 is CHs, R9 is H and R10 is H. Table 1637. Formula I.20 wherein R1 is Y-3B, R2 is CHs, R9 is CH3 and R10 is H. Table 1638. Formula I.20 wherein R1 is Y-3B, R2 is CHs, R9 is CHs and R10 is CH3. Table 1639. Formula I.20 wherein R1 is Y-3C, R2 is CHs, R9 is H and R10 is H. Table 1640. Formula 1.20 wherein R1 is Y-3C, R2 is CHs, R9 is CH3 and R10 is H. Table 1641 . Formula 1.20 wherein R1 is Y-3C, R2 is CHs, R9 is CHs and R10 is CH3. Table 1642. Formula 1.20 wherein R1 is Y-3D, R2 is CHs, R9 is H and R10 is H. Table 1643. Formula I.20 wherein R1 is Y-3D, R2 is CHs, R9 is CH3 and R10 is H. Table 1644. Formula 1.20 wherein R1 is Y-3D, R2 is CHs, R9 is CHs and R10 is CH3. Table 1645. Formula 1.20 wherein R1 is Y-4A, R2 is CHs, R9 is H and R10 is H. Table 1646. Formula 1.20 wherein R1 is Y-4A, R2 is CHs, R9 is CH3 and R10 is H. Table 1647. Formula 1.20 wherein R1 is Y-4A, R2 is CHs, R9 is CHs and R10 is CH3. Table 1648. Formula I.20 wherein R1 is Y-4B, R2 is CHs, R9 is H and R10 is H. Table 1649. Formula I.20 wherein R1 is Y-4B, R2 is CHs, R9 is CH3 and R10 is H. Table 1650. Formula I.20 wherein R1 is Y-4B, R2 is CHs, R9 is CHs and R10 is CH3. Table 1651 . Formula I.20 wherein R1 is Y-4C, R2 is CHs, R9 is H and R10 is H. Table 1652. Formula I.20 wherein R1 is Y-4C, R2 is CHs, R9 is CH3 and R10 is H. Table 1653. Formula I.20 wherein R1 is Y-4C, R2 is CHs, R9 is CHs and R10 is CH3. Table 1654. Formula I.20 wherein R1 is Y-4D, R2 is CHs, R9 is H and R10 is H. Table 1655. Formula I.20 wherein R1 is Y-4D, R2 is CHs, R9 is CH3 and R10 is H. Table 1656. Formula I.20 wherein R1 is Y-4D, R2 is CHs, R9 is CHs and R10 is CH3. Table 1657. Formula 1.20 wherein R1 is Y-5A, R2 is CHs, R9 is H and R10 is H. Table 1658. Formula 1.20 wherein R1 is Y-5A, R2 is CHs, R9 is CH3 and R10 is H. Table 1659. Formula 1.20 wherein R1 is Y-5A, R2 is CHs, R9 is CHs and R10 is CH3. Table 1660. Formula I.20 wherein R1 is Y-5B, R2 is CHs, R9 is H and R10 is H. Table 1661 . Formula I.20 wherein R1 is Y-5B, R2 is CHs, R9 is CH3 and R10 is H. Table 1662. Formula I.20 wherein R1 is Y-5B, R2 is CHs, R9 is CHs and R10 is CH3. Table 1663. Formula 1.20 wherein R1 is Y-6A, R2 is CHs, R9 is H and R10 is H.

Table 1664. Formula I.20 wherein R1 is Y-6A, R2 is CH3, R9 is CH3 and R10 is H.

Table 1665. Formula 1.20 wherein R1 is Y-6A, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 1666. Formula I.20 wherein R1 is Y-6B, R2 is CH3, R9 is H and R10 is H.

Table 1667. Formula I.20 wherein R1 is Y-6B, R2 is CH3, R9 is CH3 and R10 is H.

Table 1668. Formula I.20 wherein R1 is Y-6B, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 1669. Formula I.20 wherein R1 is Y-7A, R2 is CH3, R9 is H and R10 is H.

Table 1670. Formula I.20 wherein R1 is Y-7A, R2 is CH3, R9 is CH3 and R10 is H.

Table 1671 . Formula I.20 wherein R1 is Y-7A, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 1672. Formula I.20 wherein R1 is Y-7B, R2 is CH3, R9 is H and R10 is H.

Table 1673. Formula I.20 wherein R1 is Y-7B, R2 is CH3, R9 is CH3 and R10 is H.

Table 1674. Formula I.20 wherein R1 is Y-7B, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 1675. Formula I.20 wherein R1 is Y-8A, R2 is CH3, R9 is H and R10 is H.

Table 1676. Formula I.20 wherein R1 is Y-8A, R2 is CH3, R9 is CH3 and R10 is H.

Table 1677. Formula I.20 wherein R1 is Y-8A, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 1678. Formula I.20 wherein R1 is Y-8B, R2 is CH3, R9 is H and R10 is H.

Table 1679. Formula I.20 wherein R1 is Y-8B, R2 is CH3, R9 is CH3 and R10 is H.

Table 1680. Formula I.20 wherein R1 is Y-8B, R2 is CH3, R9 is CH3 and R10 is CH3.

Table 1681 . Formula I.20 wherein R1 is Y-1 A, R2 is C2H5, R9 is H and R10 is H. Table 1682. Formula I.20 wherein R1 is Y-1 A, R2 is C2H5, R9 is CH3 and R10 is H.

Table 1683. Formula I.20 wherein R1 is Y-1 A, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 1684. Formula I.20 wherein R1 is Y-1 B, R2 is C2H5, R9 is H and R10 is H. Table 1685. Formula I.20 wherein R1 is Y-1 B, R2 is C2H5, R9 is CH3 and R10 is H.

Table 1686. Formula I.20 wherein R1 is Y-1 B, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 1687. Formula I.20 wherein R1 is Y-2A, R2 is C2H5, R9 is H and R10 is H. Table 1688. Formula I.20 wherein R1 is Y-2A, R2 is C2H5, R9 is CH3 and R10 is H.

Table 1689. Formula 1.20 wherein R1 is Y-2A, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 1690. Formula I.20 wherein R1 is Y-2B, R2 is C2H5, R9 is H and R10 is H. Table 1691 . Formula I.20 wherein R1 is Y-2B, R2 is C2H5, R9 is CH3 and R10 is H.

Table 1692. Formula I.20 wherein R1 is Y-2B, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 1693. Formula I.20 wherein R1 is Y-3A, R2 is C2H5, R9 is H and R10 is H. Table 1694. Formula I.20 wherein R1 is Y-3A, R2 is C2H5, R9 is CH3 and R10 is H.

Table 1695. Formula 1.20 wherein R1 is Y-3A, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 1696. Formula I.20 wherein R1 is Y-3B, R2 is C2H5, R9 is H and R10 is H. Table 1697. Formula I.20 wherein R1 is Y-3B, R2 is C2H5, R9 is CH3 and R10 is H.

Table 1698. Formula I.20 wherein R1 is Y-3B, R2 is C2H5, R9 is CH3 and R10 is CH3.

Table 1699. Formula I.20 wherein R1 is Y-3C, R2 is C2H5, R9 is H and R10 is H.

Table 1700. Formula I.20 wherein R1 is Y-3C, R2 is C2H5, R9 is CHs and R10 is H. Table 1701 . Formula I.20 wherein R1 is Y-3C, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1702. Formula I.20 wherein R1 is Y-3D, R2 is C2H5, R9 is H and R10 is H. Table 1703. Formula I.20 wherein R1 is Y-3D, R2 is C2H5, R9 is CH3 and R10 is H. Table 1704. Formula I.20 wherein R1 is Y-3D, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1705. Formula 1.20 wherein R1 is Y-4A, R2 is C2H5, R9 is H and R10 is H. Table 1706. Formula I.20 wherein R1 is Y-4A, R2 is C2H5, R9 is CH3 and R10 is H. Table 1707. Formula 1.20 wherein R1 is Y-4A, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1708. Formula I.20 wherein R1 is Y-4B, R2 is C2H5, R9 is H and R10 is H. Table 1709. Formula I.20 wherein R1 is Y-4B, R2 is C2H5, R9 is CH3 and R10 is H. Table 1710. Formula I.20 wherein R1 is Y-4B, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 171 1 . Formula I.20 wherein R1 is Y-4C, R2 is C2H5, R9 is H and R10 is H. Table 1712. Formula I.20 wherein R1 is Y-4C, R2 is C2H5, R9 is CH3 and R10 is H. Table 1713. Formula I.20 wherein R1 is Y-4C, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1714. Formula I.20 wherein R1 is Y-4D, R2 is C2H5, R9 is H and R10 is H. Table 1715. Formula I.20 wherein R1 is Y-4D, R2 is C2H5, R9 is CH3 and R10 is H. Table 1716. Formula I.20 wherein R1 is Y-4D, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1717. Formula I.20 wherein R1 is Y-5A, R2 is C2H5, R9 is H and R10 is H. Table 1718. Formula 1.20 wherein R1 is Y-5A, R2 is C2H5, R9 is CH3 and R10 is H. Table 1719. Formula 1.20 wherein R1 is Y-5A, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1720. Formula I.20 wherein R1 is Y-5B, R2 is C2H5, R9 is H and R10 is H. Table 1721 . Formula 1.20 wherein R1 is Y-5B, R2 is C2H5, R9 is CH3 and R10 is H. Table 1722. Formula 1.20 wherein R1 is Y-5B, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1723. Formula 1.20 wherein R1 is Y-6A, R2 is C2H5, R9 is H and R10 is H. Table 1724. Formula 1.20 wherein R1 is Y-6A, R2 is C2H5, R9 is CH3 and R10 is H. Table 1725. Formula 1.20 wherein R1 is Y-6A, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1726. Formula I.20 wherein R1 is Y-6B, R2 is C2H5, R9 is H and R10 is H. Table 1727. Formula 1.20 wherein R1 is Y-6B, R2 is C2H5, R9 is CH3 and R10 is H. Table 1728. Formula I.20 wherein R1 is Y-6B, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1729. Formula 1.20 wherein R1 is Y-7A, R2 is C2H5, R9 is H and R10 is H. Table 1730. Formula 1.20 wherein R1 is Y-7A, R2 is C2H5, R9 is CH3 and R10 is H. Table 1731 . Formula 1.20 wherein R1 is Y-7A, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1732. Formula I.20 wherein R1 is Y-7B, R2 is C2H5, R9 is H and R10 is H. Table 1733. Formula I.20 wherein R1 is Y-7B, R2 is C2H5, R9 is CH3 and R10 is H. Table 1734. Formula I.20 wherein R1 is Y-7B, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1735. Formula I.20 wherein R1 is Y-8A, R2 is C2H5, R9 is H and R10 is H.

Table 1736. Formula 1.20 wherein R1 is Y-8A, R2 is C2H5, R9 is CHs and R10 is H. Table 1737. Formula 1.20 wherein R1 is Y-8A, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1738. Formula I.20 wherein R1 is Y-8B, R2 is C2H5, R9 is H and R10 is H.

Table 1739. Formula I.20 wherein R1 is Y-8B, R2 is C2H5, R9 is CH3 and R10 is H. Table 1740. Formula I.20 wherein R1 is Y-8B, R2 is C2H5, R9 is CH3 and R10 is CH3. Table 1741 . Formula I.20 wherein R1 is Y-1A, R2 is C-C3H5, R9 is H and R10 is H. Table 1742. Formula 1.20 wherein R1 is Y-1A, R2 is C-C3H5, R9 is CH3 and R10 is H. Table 1743. Formula 1.20 wherein R1 is Y-1A, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 1744. Formula I.20 wherein R1 is Y-1 B, R2 is C-C3H5, R9 is H and R10 is H. Table 1745. Formula I.20 wherein R1 is Y-1 B, R2 is C-C3H5, R9 is CH3, R10 is H.

Table 1746. Formula I.20 wherein R1 is Y-1 B, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 1747. Formula 1.20 wherein R1 is Y-2A, R2 is C-C3H5, R9 is H and R10 is H. Table 1748. Formula 1.20 wherein R1 is Y-2A, R2 is C-C3H5, R9 is CH3 and R10 is H. Table 1749. Formula 1.20 wherein R1 is Y-2A, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 1750. Formula I.20 wherein R1 is Y-2B, R2 is C-C3H5, R9 is H and R10 is H. Table 1751 . Formula 1.20 wherein R1 is Y-2B, R2 is C-C3H5, R9 is CH3 and R10 is H. Table 1752. Formula 1.20 wherein R1 is Y-2B, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 1753. Formula I.20 wherein R1 is Y-3A, R2 is C-C3H5, R9 is H and R10 is H. Table 1754. Formula 1.20 wherein R1 is Y-3A, R2 is C-C3H5, R9 is CH3 and R10 is H. Table 1755. Formula 1.20 wherein R1 is Y-3A, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 1756. Formula I.20 wherein R1 is Y-3B, R2 is C-C3H5, R9 is H and R10 is H. Table 1757. Formula I.20 wherein R1 is Y-3B, R2 is C-C3H5, R9 is CH3 and R10 is H. Table 1758. Formula I.20 wherein R1 is Y-3B, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 1759. Formula I.20 wherein R1 is Y-3C, R2 is C-C3H5, R9 is H and R10 is H. Table 1760. Formula 1.20 wherein R1 is Y-3C, R2 is C-C3H5, R9 is CH3 and R10 is H. Table 1761 . Formula I.20 wherein R1 is Y-3C, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 1762. Formula I.20 wherein R1 is Y-3D, R2 is C-C3H5, R9 is H and R10 is H. Table 1763. Formula I.20 wherein R1 is Y-3D, R2 is C-C3H5, R9 is CH3 and R10 is H. Table 1764. Formula I.20 wherein R1 is Y-3D, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 1765. Formula 1.20 wherein R1 is Y-4A, R2 is C-C3H5, R9 is H and R10 is H. Table 1766. Formula I.20 wherein R1 is Y-4A, R2 is C-C3H5, R9 is CH3 and R10 is H. Table 1767. Formula 1.20 wherein R1 is Y-4A, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 1768. Formula I.20 wherein R1 is Y-4B, R2 is C-C3H5, R9 is H and R10 is H. Table 1769. Formula I.20 wherein R1 is Y-4B, R2 is C-C3H5, R9 is CH3 and R10 is H. Table 1770. Formula I.20 wherein R1 is Y-4B, R2 is C-C3H5, R9 is CH3 and R10 is CH3. Table 1771 . Formula 1.20 wherein R1 is Y-4C, R2 is C-C3H5, R9 is H and R10 is H.

Table 1772. Formula I.20 wherein R1 is Y-4C, R2 is c-C3H5, R9 is CH3 and R10 is H.

Table 1773. Formula I.20 wherein R1 is Y-4C, R2 is c-C3H5, R9 is CH3 and R10 is CH3.

Table 1774. Formula I.20 wherein R1 is Y-4D, R2 is c-C3H5, R9 is H and R10 is H.

Table 1775. Formula I.20 wherein R1 is Y-4D, R2 is c-C3H5, R9 is CH3 and R10 is H.

Table 1776. Formula I.20 wherein R1 is Y-4D, R2 is c-C3H5, R9 is CH3 and R10 is CH3.

Table 1777. Formula I.20 wherein R1 is Y-5A, R2 is c-C3H5, R9 is H and R10 is H.

Table 1778. Formula I.20 wherein R1 is Y-5A, R2 is c-C3H5, R9 is CH3 and R10 is H.

Table 1779. Formula 1.20 wherein R1 is Y-5A, R2 is c-C3H5, R9 is CH3 and R10 is CH3.

Table 1780. Formula I.20 wherein R1 is Y-5B, R2 is c-C3H5, R9 is H and R10 is H.

Table 1781 . Formula I.20 wherein R1 is Y-5B, R2 is c-C3H5, R9 is CH3 and R10 is H.

Table 1782. Formula I.20 wherein R1 is Y-5B, R2 is c-C3H5, R9 is CH3 and R10 is CH3.

Table 1783. Formula I.20 wherein R1 is Y-6A, R2 is c-C3H5, R9 is H and R10 is H.

Table 1784. Formula I.20 wherein R1 is Y-6A, R2 is c-C3H5, R9 is CH3 and R10 is H.

Table 1785. Formula 1.20 wherein R1 is Y-6A, R2 is c-C3H5, R9 is CH3 and R10 is CH3.

Table 1786. Formula I.20 wherein R1 is Y-6B, R2 is c-C3H5, R9 is H and R10 is H.

Table 1787. Formula I.20 wherein R1 is Y-6B, R2 is c-C3H5, R9 is CH3 and R10 is H.

Table 1788. Formula I.20 wherein R1 is Y-6B, R2 is c-C3H5, R9 is CH3 and R10 is CH3.

Table 1789. Formula I.20 wherein R1 is Y-7A, R2 is c-C3H5, R9 is H and R10 is H.

Table 1790. Formula I.20 wherein R1 is Y-7A, R2 is c-C3H5, R9 is CH3 and R10 is H.

Table 1791 . Formula 1.20 wherein R1 is Y-7A, R2 is c-C3H5, R9 is CH3 and R10 is CH3.

Table 1792. Formula I.20 wherein R1 is Y-7B, R2 is c-C3H5, R9 is H and R10 is H.

Table 1793. Formula I.20 wherein R1 is Y-7B, R2 is c-C3H5, R9 is CH3 and R10 is H.

Table 1794. Formula I.20 wherein R1 is Y-7B, R2 is c-C3H5, R9 is CH3 and R10 is CH3.

Table 1795. Formula I.20 wherein R1 is Y-8A, R2 is c-C3H5, R9 is H and R10 is H.

Table 1796. Formula I.20 wherein R1 is Y-8A, R2 is c-C3H5, R9 is CH3 and R10 is H.

Table 1797. Formula 1.20 wherein R1 is Y-8A, R2 is c-C3H5, R9 is CH3 and R10 is CH3.

Table 1798. Formula I.20 wherein R1 is Y-8B, R2 is c-C3H5, R9 is H and R10 is H.

Table 1799. Formula I.20 wherein R1 is Y-8B, R2 is c-C3H5, R9 is CH3 and R10 is H.

Table 1800. Formula I.20 wherein R1 is Y-8B, R2 is c-C3H5, R9 is CH3 and R10 is CH3.

Table 1801 . Formula I.25 wherein R1 is Y-1A and R2 is H.

Table 1802. Formula I.25 wherein R1 is Y-1 B and R2 is H.

Table 1803. Formula I.25 wherein R1 is Y-2A and R2 is H.

Table 1804. Formula I.25 wherein R1 is Y-2B and R2 is H.

Table 1805. Formula I.25 wherein R1 is Y-3A and R2 is H.

Table 1806. Formula I.25 wherein R1 is Y-3B and R2 is H.

Table 1807. Formula I.25 wherein R1 is Y-3C and R2 is H.

Table 1808. Formula I.25 wherein R1 is Y-3D and R2 is H.

Table 1809. Formula I.25 wherein R1 is Y-4A and R2 is H.

Table 1810. Formula I.25 wherein R1 is Y-4B and R2 is H.

Table 181 1 . Formula I.25 wherein R1 is Y-4C and R2 is H.

Table 1812. Formula I.25 wherein R1 is Y-4D and R2 is H.

Table 1813. Formula I.25 wherein R1 is Y-5A and R2 is H.

Table 1814. Formula I.25 wherein R1 is Y-5B and R2 is H.

Table 1815. Formula I.25 wherein R1 is Y-6A and R2 is H.

Table 1816. Formula I.25 wherein R1 is Y-6B and R2 is H.

Table 1817. Formula I.25 wherein R1 is Y-7A and R2 is H.

Table 1818. Formula I.25 wherein R1 is Y-7B and R2 is H.

Table 1819. Formula I.25 wherein R1 is Y-8A and R2 is H.

Table 1820. Formula I.25 wherein R1 is Y-8B and R2 is H.

Table 1821 . Formula I.25 wherein R1 is Y-1A and R2 is CH3. Table 1822. Formula I.25 wherein R1 is Y-1 B and R2 is CH3.

Table 1823. Formula 1.25 wherein R1 is Y-2A and R2 is CH3.

Table 1824. Formula 1.25 wherein R1 is Y-2B and R2 is CH3.

Table 1825. Formula I.25 wherein R1 is Y-3A and R2 is CH3.

Table 1826. Formula I.25 wherein R1 is Y-3B and R2 is CH3.

Table 1827. Formula I.25 wherein R1 is Y-3C and R2 is CH3.

Table 1828. Formula I.25 wherein R1 is Y-3D and R2 is CH3.

Table 1829. Formula I.25 wherein R1 is Y-4A and R2 is CH3.

Table 1830. Formula I.25 wherein R1 is Y-4B and R2 is CH3.

Table 1831 . Formula I.25 wherein R1 is Y-4C and R2 is CH3.

Table 1832. Formula I.25 wherein R1 is Y-4D and R2 is CH3.

Table 1833. Formula I.25 wherein R1 is Y-5A and R2 is CH3.

Table 1834. Formula I.25 wherein R1 is Y-5B and R2 is CH3.

Table 1835. Formula I.25 wherein R1 is Y-6A and R2 is CH3.

Table 1836. Formula I.25 wherein R1 is Y-6B and R2 is CH3.

Table 1837. Formula 1.25 wherein R1 is Y-7A and R2 is CH3.

Table 1838. Formula I.25 wherein R1 is Y-7B and R2 is CH3.

Table 1839. Formula 1.25 wherein R1 is Y-8A and R2 is CH3.

Table 1840. Formula I.25 wherein R1 is Y-8B and R2 is CH3.

Table 1841 . Formula I.25 wherein R1 is Y-1 A and R2 is c-C3H5.

Table 1842. Formula I.25 wherein R1 is Y-1 B and R2 is c-C3H5.

Table 1843. Formula 1.25 wherein R1 is Y-2A and R2 is c-C3H5.

Table 1844. Formula 1.25 wherein R1 is Y-2B and R2 is C-C3H5.

Table 1845. Formula 1.25 wherein R1 is Y-3A and R2 is C-C3H5.

Table 1846. Formula I.25 wherein R1 is Y-3B and R2 is C-C3H5.

Table 1847. Formula I.25 wherein R1 is Y-3C and R2 is C-C3H5.

Table 1848. Formula I.25 wherein R1 is Y-3D and R2 is C-C3H5.

Table 1849. Formula 1.25 wherein R1 is Y-4A and R2 is C-C3H5.

Table 1850. Formula I.25 wherein R1 is Y-4B and R2 is C-C3H5.

Table 1851 . Formula 1.25 wherein R1 is Y-4C and R2 is C-C3H5.

Table 1852. Formula 1.25 wherein R1 is Y-4D and R2 is C-C3H5.

Table 1853. Formula 1.25 wherein R1 is Y-5A and R2 is C-C3H5.

Table 1854. Formula 1.25 wherein R1 is Y-5B and R2 is C-C3H5.

Table 1855. Formula 1.25 wherein R1 is Y-6A and R2 is C-C3H5.

Table 1856. Formula I.25 wherein R1 is Y-6B and R2 is C-C3H5.

Table 1857. Formula 1.25 wherein R1 is Y-7A and R2 is C-C3H5.

Table 1858. Formula I.25 wherein R1 is Y-7B and R2 is C-C3H5.

Table 1859. Formula 1.25 wherein R1 is Y-8A and R2 is C-C3H5.

Table 1860. Formula I.25 wherein R1 is Y-8B and R2 is C-C3H5.

Table 1861 . Formula I.26 wherein R1 is Y-1A and R2 is H.

Table 1862. Formula I.26 wherein R1 is Y-1 B and R2 is H.

Table 1863. Formula I.26 wherein R1 is Y-2A and R2 is H.

Table 1864. Formula I.26 wherein R1 is Y-2B and R2 is H.

Table 1865. Formula I.26 wherein R1 is Y-3A and R2 is H.

Table 1866. Formula I.26 wherein R1 is Y-3B and R2 is H.

Table 1867. Formula I.26 wherein R1 is Y-3C and R2 is H.

Table 1868. Formula I.26 wherein R1 is Y-3D and R2 is H.

Table 1869. Formula I.26 wherein R1 is Y-4A and R2 is H.

Table 1870. Formula I.26 wherein R1 is Y-4B and R2 is H.

Table 1871 . Formula I.26 wherein R1 is Y-4C and R2 is H.

Table 1872. Formula I.26 wherein R1 is Y-4D and R2 is H.

Table 1873. Formula I.26 wherein R1 is Y-5A and R2 is H.

Table 1874. Formula I.26 wherein R1 is Y-5B and R2 is H.

Table 1875. Formula I.26 wherein R1 is Y-6A and R2 is H.

Table 1876. Formula I.26 wherein R1 is Y-6B and R2 is H.

Table 1877. Formula I.26 wherein R1 is Y-7A and R2 is H.

Table 1878. Formula I.26 wherein R1 is Y-7B and R2 is H.

Table 1879. Formula I.26 wherein R1 is Y-8A and R2 is H.

Table 1880. Formula I.26 wherein R1 is Y-8B and R2 is H.

Table 1881 . Formula I.26 wherein R1 is Y-1 A and R2 is CH3.

Table 1882. Formula I.26 wherein R1 is Y-1 B and R2 is CH3.

Table 1883. Formula 1.26 wherein R1 is Y-2A and R2 is CH3.

Table 1884. Formula I.26 wherein R1 is Y-2B and R2 is CH3.

Table 1885. Formula 1.26 wherein R1 is Y-3A and R2 is CH3.

Table 1886. Formula I.26 wherein R1 is Y-3B and R2 is CH3.

Table 1887. Formula I.26 wherein R1 is Y-3C and R2 is CH3.

Table 1888. Formula I.26 wherein R1 is Y-3D and R2 is CH3.

Table 1889. Formula I.26 wherein R1 is Y-4A and R2 is CH3.

Table 1890. Formula I.26 wherein R1 is Y-4B and R2 is CH3.

Table 1891 . Formula I.26 wherein R1 is Y-4C and R2 is CH3.

Table 1892. Formula I.26 wherein R1 is Y-4D and R2 is CH3.

Table 1893. Formula 1.26 wherein R1 is Y-5A and R2 is CH3.

Table 1894. Formula I.26 wherein R1 is Y-5B and R2 is CH3.

Table 1895. Formula I.26 wherein R1 is Y-6A and R2 is CH3.

Table 1896. Formula I.26 wherein R1 is Y-6B and R2 is CH3.

Table 1897. Formula 1.26 wherein R1 is Y-7A and R2 is CH3.

Table 1898. Formula I.26 wherein R1 is Y-7B and R2 is CH3.

Table 1899. Formula I.26 wherein R1 is Y-8A and R2 is CH3.

Table 1900. Formula I.26 wherein R1 is Y-8B and R2 is CH3.

Table 1901 . Formula I.26 wherein R1 is Y-1 A and R2 is c-C3H5.

Table 1902. Formula I.26 wherein R1 is Y-1 B and R2 is c-C3H5.

Table 1903. Formula 1.26 wherein R1 is Y-2A and R2 is c-C3H5.

Table 1904. Formula I.26 wherein R1 is Y-2B and R2 is c-C3H5.

Table 1905. Formula 1.26 wherein R1 is Y-3A and R2 is c-C3H5.

Table 1906. Formula I.26 wherein R1 is Y-3B and R2 is c-C3H5.

Table 1907. Formula I.26 wherein R1 is Y-3C and R2 is c-C3H5.

Table 1908. Formula I.26 wherein R1 is Y-3D and R2 is c-C3H5.

Table 1909. Formula 1.26 wherein R1 is Y-4A and R2 is c-C3H5.

Table 1910. Formula I.26 wherein R1 is Y-4B and R2 is c-C3H5.

Table 191 1 . Formula I.26 wherein R1 is Y-4C and R2 is c-C3H5.

Table 1912. Formula I.26 wherein R1 is Y-4D and R2 is c-C3H5.

Table 1913. Formula 1.26 wherein R1 is Y-5A and R2 is c-C3H5.

Table 1914. Formula I.26 wherein R1 is Y-5B and R2 is c-C3H5.

Table 1915. Formula I.26 wherein R1 is Y-6A and R2 is c-C3H5.

Table 1916. Formula I.26 wherein R1 is Y-6B and R2 is C-C3H5.

Table 1917. Formula I.26 wherein R1 is Y-7A and R2 is C-C3H5.

Table 1918. Formula I.26 wherein R1 is Y-7B and R2 is C-C3H5.

Table 1919. Formula I.26 wherein R1 is Y-8A and R2 is C-C3H5.

Table 1920. Formula I.26 wherein R1 is Y-8B and R2 is C-C3H5.

Table 1921 . Formula I.29 wherein R1 is Y-1A and R2 is H.

Table 1922. Formula I.29 wherein R1 is Y-1 B and R2 is H.

Table 1923. Formula I.29 wherein R1 is Y-2A and R2 is H.

Table 1924. Formula I.29 wherein R1 is Y-2B and R2 is H.

Table 1925. Formula I.29 wherein R1 is Y-3A and R2 is H.

Table 1926. Formula I.29 wherein R1 is Y-3B and R2 is H.

Table 1927. Formula I.29 wherein R1 is Y-3C and R2 is H.

Table 1928. Formula I.29 wherein R1 is Y-3D and R2 is H.

Table 1929. Formula I.29 wherein R1 is Y-4A and R2 is H.

Table 1930. Formula I.29 wherein R1 is Y-4B and R2 is H.

Table 1931 . Formula I.29 wherein R1 is Y-4C and R2 is H.

Table 1932. Formula I.29 wherein R1 is Y-4D and R2 is H.

Table 1933. Formula I.29 wherein R1 is Y-5A and R2 is H.

Table 1934. Formula I.29 wherein R1 is Y-5B and R2 is H.

Table 1935. Formula I.29 wherein R1 is Y-6A and R2 is H.

Table 1936. Formula I.29 wherein R1 is Y-6B and R2 is H.

Table 1937. Formula I.29 wherein R1 is Y-7A and R2 is H.

Table 1938. Formula I.29 wherein R1 is Y-7B and R2 is H.

Table 1939. Formula I.29 wherein R1 is Y-8A and R2 is H.

Table 1940. Formula I.29 wherein R1 is Y-8B and R2 is H.

Table 1941 . Formula I.29 wherein R1 is Y-1 A and R2 is CH3.

Table 1942. Formula I.29 wherein R1 is Y-1 B and R2 is CH3.

Table 1943. Formula 1.29 wherein R1 is Y-2A and R2 is CH3.

Table 1944. Formula I.29 wherein R1 is Y-2B and R2 is CH3.

Table 1945. Formula I.29 wherein R1 is Y-3A and R2 is CH3.

Table 1946. Formula I.29 wherein R1 is Y-3B and R2 is CH3.

Table 1947. Formula I.29 wherein R1 is Y-3C and R2 is CH3.

Table 1948. Formula I.29 wherein R1 is Y-3D and R2 is CH3.

Table 1949. Formula I.29 wherein R1 is Y-4A and R2 is CH3.

Table 1950. Formula I.29 wherein R1 is Y-4B and R2 is CH3.

Table 1951 . Formula 1.29 wherein R1 is Y-4C and R2 is CH3.

Table 1952. Formula 1.29 wherein R1 is Y-4D and R2 is CH3. Table 1953. Formula I.29 wherein R1 is Y-5A and R2 is CH3. Table 1954. Formula I.29 wherein R1 is Y-5B and R2 is CH3. Table 1955. Formula I.29 wherein R1 is Y-6A and R2 is CH3. Table 1956. Formula I.29 wherein R1 is Y-6B and R2 is CH3. Table 1957. Formula 1.29 wherein R1 is Y-7A and R2 is CH3. Table 1958. Formula I.29 wherein R1 is Y-7B and R2 is CH3. Table 1959. Formula I.29 wherein R1 is Y-8A and R2 is CH3. Table 1960. Formula I.29 wherein R1 is Y-8B and R2 is CH3. Table 1961 . Formula I.29 wherein R1 is Y-1 A and R2 is C-C3H5. Table 1962. Formula I.29 wherein R1 is Y-1 B and R2 is C-C3H5. Table 1963. Formula 1.29 wherein R1 is Y-2A and R2 is C-C3H5. Table 1964. Formula I.29 wherein R1 is Y-2B and R2 is C-C3H5. Table 1965. Formula 1.29 wherein R1 is Y-3A and R2 is C-C3H5. Table 1966. Formula I.29 wherein R1 is Y-3B and R2 is C-C3H5. Table 1967. Formula I.29 wherein R1 is Y-3C and R2 is C-C3H5. Table 1968. Formula I.29 wherein R1 is Y-3D and R2 is C-C3H5. Table 1969. Formula 1.29 wherein R1 is Y-4A and R2 is C-C3H5. Table 1970. Formula I.29 wherein R1 is Y-4B and R2 is C-C3H5. Table 1971 . Formula 1.29 wherein R1 is Y-4C and R2 is C-C3H5. Table 1972. Formula I.29 wherein R1 is Y-4D and R2 is C-C3H5. Table 1973. Formula 1.29 wherein R1 is Y-5A and R2 is C-C3H5. Table 1974. Formula I.29 wherein R1 is Y-5B and R2 is C-C3H5. Table 1975. Formula 1.29 wherein R1 is Y-6A and R2 is C-C3H5. Table 1976. Formula I.29 wherein R1 is Y-6B and R2 is C-C3H5. Table 1977. Formula 1.29 wherein R1 is Y-7A and R2 is c-C3H5. Table 1978. Formula I.29 wherein R1 is Y-7B and R2 is C-C3H5. Table 1979. Formula I.29 wherein R1 is Y-8A and R2 is C-C3H5. Table 1980. Formula I.29 wherein R1 is Y-8B and R2 is C-C3H5. Table 1981 . Formula 1.30 wherein R1 is Y-1 A and R2 is H. Table 1982. Formula 1.30 wherein R1 is Y-1 B and R2 is H. Table 1983. Formula 1.30 wherein R1 is Y-2A and R2 is H. Table 1984. Formula 1.30 wherein R1 is Y-2B and R2 is H. Table 1985. Formula 1.30 wherein R1 is Y-3A and R2 is H. Table 1986. Formula 1.30 wherein R1 is Y-3B and R2 is H. Table 1987. Formula I.30 wherein R1 is Y-3C and R2 is H.

Table 1988. Formula 1.30 wherein R1 is Y-3D and R2 is H.

Table 1989. Formula 1.30 wherein R1 is Y-4A and R2 is H.

Table 1990. Formula 1.30 wherein R1 is Y-4B and R2 is H.

Table 1991 . Formula 1.30 wherein R1 is Y-4C and R2 is H.

Table 1992. Formula 1.30 wherein R1 is Y-4D and R2 is H.

Table 1993. Formula 1.30 wherein R1 is Y-5A and R2 is H.

Table 1994. Formula 1.30 wherein R1 is Y-5B and R2 is H.

Table 1995. Formula 1.30 wherein R1 is Y-6A and R2 is H.

Table 1996. Formula 1.30 wherein R1 is Y-6B and R2 is H.

Table 1997. Formula 1.30 wherein R1 is Y-7A and R2 is H.

Table 1998. Formula 1.30 wherein R1 is Y-7B and R2 is H.

Table 1999. Formula 1.30 wherein R1 is Y-8A and R2 is H.

Table 2000. Formula 1.30 wherein R1 is Y-8B and R2 is H.

Table 2001 . Formula I.30 wherein R1 is Y-1 A and R2 is CH3.

Table 2002. Formula I.30 wherein R1 is Y-1 B and R2 is CH3.

Table 2003. Formula 1.30 wherein R1 is Y-2A and R2 is CH3.

Table 2004. Formula I.30 wherein R1 is Y-2B and R2 is CH3.

Table 2005. Formula 1.30 wherein R1 is Y-3A and R2 is CH3.

Table 2006. Formula I.30 wherein R1 is Y-3B and R2 is CH3.

Table 2007. Formula I.30 wherein R1 is Y-3C and R2 is CH3.

Table 2008. Formula I.30 wherein R1 is Y-3D and R2 is CH3.

Table 2009. Formula 1.30 wherein R1 is Y-4A and R2 is CH3.

Table 2010. Formula I.30 wherein R1 is Y-4B and R2 is CH3.

Table 201 1 . Formula I.30 wherein R1 is Y-4C and R2 is CH3.

Table 2012. Formula I.30 wherein R1 is Y-4D and R2 is CH3.

Table 2013. Formula I.30 wherein R1 is Y-5A and R2 is CH3.

Table 2014. Formula I.30 wherein R1 is Y-5B and R2 is CH3.

Table 2015. Formula I.30 wherein R1 is Y-6A and R2 is CH3.

Table 2016. Formula I.30 wherein R1 is Y-6B and R2 is CH3.

Table 2017. Formula I.30 wherein R1 is Y-7A and R2 is CH3.

Table 2018. Formula I.30 wherein R1 is Y-7B and R2 is CH3.

Table 2019. Formula I.30 wherein R1 is Y-8A and R2 is CH3.

Table 2020. Formula I.30 wherein R1 is Y-8B and R2 is CH3.

Table 2021 . Formula 1.30 wherein R1 is Y-1 A and R2 is c-C3H5.

Table 2022. Formula 1.30 wherein R1 is Y-1 B and R2 is c-C3H5.

Table 2023. Formula 1.30 wherein R1 is Y-2A and R2 is c-C3H5.

Table 2024. Formula 1.30 wherein R1 is Y-2B and R2 is C-C3H5.

Table 2025. Formula 1.30 wherein R1 is Y-3A and R2 is C-C3H5.

Table 2026. Formula 1.30 wherein R1 is Y-3B and R2 is C-C3H5.

Table 2027. Formula 1.30 wherein R1 is Y-3C and R2 is C-C3H5.

Table 2028. Formula 1.30 wherein R1 is Y-3D and R2 is C-C3H5.

Table 2029. Formula 1.30 wherein R1 is Y-4A and R2 is C-C3H5.

Table 2030. Formula 1.30 wherein R1 is Y-4B and R2 is C-C3H5.

Table 2031 . Formula 1.30 wherein R1 is Y-4C and R2 is C-C3H5.

Table 2032. Formula 1.30 wherein R1 is Y-4D and R2 is C-C3H5.

Table 2033. Formula 1.30 wherein R1 is Y-5A and R2 is C-C3H5.

Table 2034. Formula 1.30 wherein R1 is Y-5B and R2 is C-C3H5.

Table 2035. Formula 1.30 wherein R1 is Y-6A and R2 is C-C3H5.

Table 2036. Formula 1.30 wherein R1 is Y-6B and R2 is C-C3H5.

Table 2037. Formula 1.30 wherein R1 is Y-7A and R2 is C-C3H5.

Table 2038. Formula 1.30 wherein R1 is Y-7B and R2 is C-C3H5.

Table 2039. Formula 1.30 wherein R1 is Y-8A and R2 is C-C3H5.

Table 2040. Formula 1.30 wherein R1 is Y-8B and R2 is C-C3H5.

Table 2041 . Formula 1.31 wherein R1 is Y-1 A and R2 is H.

Table 2042. Formula 1.31 wherein R1 is Y-1 B and R2 is H.

Table 2043. Formula 1.31 wherein R1 is Y-2A and R2 is H.

Table 2044. Formula 1.31 wherein R1 is Y-2B and R2 is H.

Table 2045. Formula 1.31 wherein R1 is Y-3A and R2 is H.

Table 2046. Formula 1.31 wherein R1 is Y-3B and R2 is H.

Table 2047. Formula 1.31 wherein R1 is Y-3C and R2 is H.

Table 2048. Formula 1.31 wherein R1 is Y-3D and R2 is H.

Table 2049. Formula 1.31 wherein R1 is Y-4A and R2 is H.

Table 2050. Formula 1.31 wherein R1 is Y-4B and R2 is H.

Table 2051 . Formula 1.31 wherein R1 is Y-4C and R2 is H.

Table 2052. Formula 1.31 wherein R1 is Y-4D and R2 is H.

Table 2053. Formula 1.31 wherein R1 is Y-5A and R2 is H.

Table 2054. Formula 1.31 wherein R1 is Y-5B and R2 is H.

Table 2055. Formula 1.31 wherein R1 is Y-6A and R2 is H.

Table 2056. Formula 1.31 wherein R1 is Y-6B and R2 is H.

Table 2057. Formula 1.31 wherein R1 is Y-7A and R2 is H.

Table 2058. Formula 1.31 wherein R1 is Y-7B and R2 is H.

Table 2059. Formula 1.31 wherein R1 is Y-8A and R2 is H.

Table 2060. Formula 1.31 wherein R1 is Y-8B and R2 is H.

Table 2061 . Formula 1.31 wherein R1 is Y-1 A and R2 is CH3.

Table 2062. Formula 1.31 wherein R1 is Y-1 B and R2 is CH3.

Table 2063. Formula 1.31 wherein R1 is Y-2A and R2 is CH3.

Table 2064. Formula 1.31 wherein R1 is Y-2B and R2 is CH3.

Table 2065. Formula 1.31 wherein R1 is Y-3A and R2 is CH3.

Table 2066. Formula 1.31 wherein R1 is Y-3B and R2 is CH3.

Table 2067. Formula 1.31 wherein R1 is Y-3C and R2 is CH3.

Table 2068. Formula 1.31 wherein R1 is Y-3D and R2 is CH3.

Table 2069. Formula 1.31 wherein R1 is Y-4A and R2 is CH3.

Table 2070. Formula 1.31 wherein R1 is Y-4B and R2 is CH3.

Table 2071 . Formula 1.31 wherein R1 is Y-4C and R2 is CH3.

Table 2072. Formula 1.31 wherein R1 is Y-4D and R2 is CH3.

Table 2073. Formula 1.31 wherein R1 is Y-5A and R2 is CH3.

Table 2074. Formula 1.31 wherein R1 is Y-5B and R2 is CH3.

Table 2075. Formula 1.31 wherein R1 is Y-6A and R2 is CH3.

Table 2076. Formula 1.31 wherein R1 is Y-6B and R2 is CH3.

Table 2077. Formula 1.31 wherein R1 is Y-7A and R2 is CH3.

Table 2078. Formula 1.31 wherein R1 is Y-7B and R2 is CH3.

Table 2079. Formula 1.31 wherein R1 is Y-8A and R2 is CH3.

Table 2080. Formula 1.31 wherein R1 is Y-8B and R2 is CH3.

Table 2081 . Formula 1.31 wherein R1 is Y-1 A and R2 is c-C3H5.

Table 2082. Formula 1.31 wherein R1 is Y-1 B and R2 is c-C3H5.

Table 2083. Formula 1.31 wherein R1 is Y-2A and R2 is c-C3H5.

Table 2084. Formula 1.31 wherein R1 is Y-2B and R2 is c-C3H5.

Table 2085. Formula 1.31 wherein R1 is Y-3A and R2 is c-C3H5.

Table 2086. Formula 1.31 wherein R1 is Y-3B and R2 is c-C3H5.

Table 2087. Formula 1.31 wherein R1 is Y-3C and R2 is c-C3H5.

Table 2088. Formula 1.31 wherein R1 is Y-3D and R2 is c-C3H5.

Table 2089. Formula 1.31 wherein R1 is Y-4A and R2 is c-C3H5.

Table 2090. Formula 1.31 wherein R1 is Y-4B and R2 is c-C3H5.

Table 2091 . Formula 1.31 wherein R1 is Y-4C and R2 is c-C3H5.

Table 2092. Formula 1.31 wherein R1 is Y-4D and R2 is c-C3H5.

Table 2093. Formula 1.31 wherein R1 is Y-5A and R2 is c-C3H5.

Table 2094. Formula 1.31 wherein R1 is Y-5B and R2 is c-C3H5.

Table 2095. Formula 1.31 wherein R1 is Y-6A and R2 is c-C3H5.

Table 2096. Formula 1.31 wherein R1 is Y-6B and R2 is C-C3H5.

Table 2097. Formula 1.31 wherein R1 is Y-7A and R2 is C-C3H5.

Table 2098. Formula 1.31 wherein R1 is Y-7B and R2 is C-C3H5.

Table 2099. Formula 1.31 wherein R1 is Y-8A and R2 is C-C3H5.

Table 2100. Formula 1.31 wherein R1 is Y-8B and R2 is C-C3H5.

Table 2101 . Formula 1.32 wherein R1 is Y-1A and R2 is H.

Table 2102. Formula I.32 wherein R1 is Y-1 B and R2 is H.

Table 2103. Formula I.32 wherein R1 is Y-2A and R2 is H.

Table 2104. Formula I.32 wherein R1 is Y-2B and R2 is H.

Table 2105. Formula 1.32 wherein R1 is Y-3A and R2 is H.

Table 2106. Formula I.32 wherein R1 is Y-3B and R2 is H.

Table 2107. Formula I.32 wherein R1 is Y-3C and R2 is H.

Table 2108. Formula I.32 wherein R1 is Y-3D and R2 is H.

Table 2109. Formula 1.32 wherein R1 is Y-4A and R2 is H.

Table 21 10. Formula 1.32 wherein R1 is Y-4B and R2 is H.

Table 21 1 1 . Formula 1.32 wherein R1 is Y-4C and R2 is H.

Table 21 12. Formula 1.32 wherein R1 is Y-4D and R2 is H.

Table 21 13. Formula 1.32 wherein R1 is Y-5A and R2 is H.

Table 21 14. Formula 1.32 wherein R1 is Y-5B and R2 is H.

Table 21 15. Formula 1.32 wherein R1 is Y-6A and R2 is H.

Table 21 16. Formula I.32 wherein R1 is Y-6B and R2 is H.

Table 21 17. Formula I.32 wherein R1 is Y-7A and R2 is H.

Table 21 18. Formula I.32 wherein R1 is Y-7B and R2 is H.

Table 21 19. Formula 1.32 wherein R1 is Y-8A and R2 is H.

Table 2120. Formula I.32 wherein R1 is Y-8B and R2 is H.

Table 2121 . Formula I.32 wherein R1 is Y-1A and R2 is CH3.

Table 2122. Formula I.32 wherein R1 is Y-1 B and R2 is CH3.

Table 2123. Formula 1.32 wherein R1 is Y-2A and R2 is CH3.

Table 2124. Formula I.32 wherein R1 is Y-2B and R2 is CH3.

Table 2125. Formula 1.32 wherein R1 is Y-3A and R2 is CH3.

Table 2126. Formula I.32 wherein R1 is Y-3B and R2 is CH3.

Table 2127. Formula I.32 wherein R1 is Y-3C and R2 is CH3.

Table 2128. Formula I.32 wherein R1 is Y-3D and R2 is CH3.

Table 2129. Formula 1.32 wherein R1 is Y-4A and R2 is CH3.

Table 2130. Formula I.32 wherein R1 is Y-4B and R2 is CH3.

Table 2131 . Formula I.32 wherein R1 is Y-4C and R2 is CH3.

Table 2132. Formula I.32 wherein R1 is Y-4D and R2 is CH3.

Table 2133. Formula 1.32 wherein R1 is Y-5A and R2 is CH3.

Table 2134. Formula I.32 wherein R1 is Y-5B and R2 is CH3.

Table 2135. Formula 1.32 wherein R1 is Y-6A and R2 is CH3.

Table 2136. Formula I.32 wherein R1 is Y-6B and R2 is CH3.

Table 2137. Formula I.32 wherein R1 is Y-7A and R2 is CH3.

Table 2138. Formula I.32 wherein R1 is Y-7B and R2 is CH3.

Table 2139. Formula I.32 wherein R1 is Y-8A and R2 is CH3.

Table 2140. Formula I.32 wherein R1 is Y-8B and R2 is CH3.

Table 2141 . Formula 1.32 wherein R1 is Y-1A and R2 is c-C3H5.

Table 2142. Formula 1.32 wherein R1 is Y-1 B and R2 is c-C3H5.

Table 2143. Formula 1.32 wherein R1 is Y-2A and R2 is c-C3H5.

Table 2144. Formula 1.32 wherein R1 is Y-2B and R2 is c-C3H5.

Table 2145. Formula 1.32 wherein R1 is Y-3A and R2 is c-C3H5.

Table 2146. Formula 1.32 wherein R1 is Y-3B and R2 is c-C3H5.

Table 2147. Formula 1.32 wherein R1 is Y-3C and R2 is c-C3H5.

Table 2148. Formula 1.32 wherein R1 is Y-3D and R2 is c-C3H5.

Table 2149. Formula 1.32 wherein R1 is Y-4A and R2 is c-C3H5.

Table 2150. Formula 1.32 wherein R1 is Y-4B and R2 is c-C3H5.

Table 2151 . Formula 1.32 wherein R1 is Y-4C and R2 is c-C3H5.

Table 2152. Formula 1.32 wherein R1 is Y-4D and R2 is c-C3H5.

Table 2153. Formula 1.32 wherein R1 is Y-5A and R2 is c-C3H5.

Table 2154. Formula 1.32 wherein R1 is Y-5B and R2 is c-C3H5.

Table 2155. Formula 1.32 wherein R1 is Y-6A and R2 is c-C3H5.

Table 2156. Formula 1.32 wherein R1 is Y-6B and R2 is c-C3H5.

Table 2157. Formula 1.32 wherein R1 is Y-7A and R2 is c-C3H5.

Table 2158. Formula 1.32 wherein R1 is Y-7B and R2 is c-C3H5.

Table 2159. Formula 1.32 wherein R1 is Y-8A and R2 is c-C3H5.

Table 2160. Formula 1.32 wherein R1 is Y-8B and R2 is c-C3H5.

Table B:

As used herein, the term“compound(s) of the present invention” or“compound(s) according to the invention” refers to the compound(s) of formula (I) as defined above, which are also referred to as“compound(s) of formula I” or“compound(s) I” or“formula I compound(s)”, and includes their salts, tautomers, stereoisomers, and N-oxides.

The present invention also relates to a mixture of at least one compound of the present invention with at least one mixing partner as defined herein after. Preferred are binary mixtures of one compound of the present invention as component I with one mixing partner as defined herein after as component II. Preferred weight ratios for such binary mixtures are from 5000:1 to 1 :5000, preferably from 1000:1 to 1 :1000, more preferably from 100:1 to

1 :100, particularly preferably from 10:1 to 1 :10. In such binary mixtures, components I and II may be used in equal amounts, or an excess of component I, or an excess of component II may be used.

Mixing partners can be selected from pesticides, in particular insecticides, nematicides, and acaricides, fungicides, herbicides, plant growth regulators, fertilizers, and the like. Preferred mixing partners are insecticides, nematicides and fungicides.

The following list M of pesticides, grouped and numbered according the Mode of Action Classification of the Insecticide Resistance Action Committee (IRAC), together with which the compounds of the present invention can be used and with which potential synergistic effects might be produced, is intended to illustrate the possible combinations, but not to impose any limitation:

M.1 Acetylcholine esterase (AChE) inhibitors from the class of: M.1 A carbamates, for example aldicarb, alanycarb, bendiocarb, benfuracarb, butocarboxim, butoxycarboxim, carbaryl, carbofuran, carbosulfan, ethiofencarb, fenobucarb, formetanate, furathiocarb, isoprocarb, methiocarb, methomyl, metolcarb, oxamyl, pirimicarb, propoxur, thiodicarb, thiofanox, trimethacarb, XMC, xylylcarb and triazamate; or from the class of M.1 B

organophosphates, for example acephate, azamethiphos, azinphos-ethyl, azinphosmethyl, cadusafos, chlorethoxyfos, chlorfenvinphos, chlormephos, chlorpyrifos, chlorpyrifos-methyl, coumaphos, cyanophos, demeton-S-methyl, diazinon, dichlorvos/ DDVP, dicrotophos, dimethoate, dimethylvinphos, disulfoton, EPN, ethion, ethoprophos, famphur, fenamiphos, fenitrothion, fenthion, fosthiazate, heptenophos, imicyafos, isofenphos, isopropyl O-(methoxyaminothio-phosphoryl) salicylate, isoxathion, malathion, mecarbam,

methamidophos, methidathion, mevinphos, monocrotophos, naled, omethoate, oxydemeton-methyl, parathion, parathion-methyl, phenthoate, phorate, phosalone, phosmet,

phosphamidon, phoxim, pirimiphos- methyl, profenofos, propetamphos, prothiofos, pyraclofos, pyridaphenthion, quinalphos, sulfotep, tebupirimfos, temephos, terbufos, tetrachlorvinphos, thiometon, triazophos, trichlorfon and vamidothion;

M.2. GABA-gated chloride channel antagonists such as: M.2A cyclodiene organochlorine compounds, as for example endosulfan or chlordane; or M.2B fiproles (phenylpyrazoles), as for example ethiprole, fipronil, flufiprole, pyrafluprole and pyriprole;

M.3 Sodium channel modulators from the class of M.3A pyrethroids, for example acrinathrin, allethrin, d-cis-trans allethrin, d-trans allethrin, bifenthrin, bioallethrin, bioallethrin S-cylclopentenyl, bioresmethrin, cycloprothrin, cyfluthrin, beta-cyfluthrin, cyhalothrin, lambda-cyhalothrin, gamma-cyhalothrin, cypermethrin, alpha-cypermethrin, beta-cypermethrin, theta-cypermethrin, zeta-cypermethrin, cyphenothrin, deltamethrin, empenthrin, esfenvalerate, etofenprox, fenpropathrin, fenvalerate, flucythrinate, flumethrin, tau-fluvalinate, halfenprox, heptafluthrin, imiprothrin, meperfluthrin,metofluthrin, momfluorothrin, permethrin, phenothrin, prallethrin, profluthrin, pyrethrin (pyrethrum), resmethrin, silafluofen, tefluthrin,

tetramethylfluthrin, tetramethrin, tralomethrin and transfluthrin; or M.3B sodium channel modulators such as DDT or methoxychlor;

M.4 Nicotinic acetylcholine receptor agonists (nAChR) from the class of M.4A

neonicotinoids, for example acetamiprid, clothianidin, cycloxaprid, dinotefuran, imidacloprid, nitenpyram, thiacloprid and thiamethoxam; or the compounds M.4A.2: (2E-)-1-[(6-Chloropyridin-3-yl)methyl]-N'-nitro-2-pentylidenehydrazinecarboximidamide; or M4.A.3: 1-[(6-Chloropyridin-3-yl)methyl]-7-methyl-8-nitro-5-propoxy-1 ,2,3,5,6,7-hexahydroimidazo[1 ,2-a]pyridine; or from the class M.4B nicotine;

M.5 Nicotinic acetylcholine receptor allosteric activators from the class of spinosyns, for example spinosad or spinetoram;

M.6 Chloride channel activators from the class of avermectins and milbemycins, for example abamectin, emamectin benzoate, ivermectin, lepimectin or milbemectin;

M.7 Juvenile hormone mimics, such as M.7A juvenile hormone analogues as hydroprene, kinoprene and methoprene; or others as M.7B fenoxycarb or M.7C pyriproxyfen;

M.8 miscellaneous non-specific (multi-site) inhibitors, for example M.8A alkyl halides as methyl bromide and other alkyl halides, or M.8B chloropicrin, or M.8C sulfuryl fluoride, or M.8D borax, or M.8E tartar emetic;

M.9 Selective homopteran feeding blockers, for example M.9B pymetrozine, or M.9C flonicamid;

M.10 Mite growth inhibitors, for example M.10A clofentezine, hexythiazox and diflovidazin, or M.10B etoxazole;

M.11 Microbial disruptors of insect midgut membranes, for example bacillus thuringiensis or bacillus sphaericus and the insecticdal proteins they produce such as bacillus thuringiensis subsp. israelensis, bacillus sphaericus, bacillus thuringiensis subsp. aizawai, bacillus thuringiensis subsp. kurstaki and bacillus thuringiensis subsp. tenebrionis, or the Bt crop proteins: CrylAb, CrylAc, Cryl Fa, Cry2Ab, mCry3A, Cry3Ab, Cry3Bb and Cry34/35Ab1 ;

M.12 Inhibitors of mitochondrial ATP synthase, for example M.12A diafenthiuron, or M.12B organotin miticides such as azocyclotin, cyhexatin or fenbutatin oxide, or M.12C propargite, or M.12D tetrad ifon;

M.13 Uncouplers of oxidative phosphorylation via disruption of the proton gradient, for example chlorfenapyr, DNOC or sulfluramid;

M.14 Nicotinic acetylcholine receptor (nAChR) channel blockers, for example nereistoxin analogues as bensultap, cartap hydrochloride, thiocyclam or thiosultap sodium;

M.15 Inhibitors of the chitin biosynthesis type 0, such as benzoylureas as for example bistrifluron, chlorfluazuron, diflubenzuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, teflubenzuron or triflu mu ron;

M.16 Inhibitors of the chitin biosynthesis type 1 , as for example buprofezin;

M.17 Moulting disruptors, Dipteran, as for example cyromazine;

M.18 Ecdyson receptor agonists such as diacylhydrazines, for example methoxyfenozide, tebufenozide, halofenozide, fufenozide or chromafenozide;

M.19 Octopamin receptor agonists, as for example amitraz;

M.20 Mitochondrial complex III electron transport inhibitors, for example M.20A

hydramethylnon, or M.20B acequinocyl, or M.20C fluacrypyrim;

M.21 Mitochondrial complex I electron transport inhibitors, for example M.21 A METI acaricides and insecticides such as fenazaquin, fenpyroximate, pyrimidifen, pyridaben, tebufenpyrad or tolfenpyrad, or M.21 B rotenone;

M.22 Voltage-dependent sodium channel blockers, for example M.22A indoxacarb, or M.22B metaflumizone, or M.22B.1 : 2-[2-(4-Cyanophenyl)-1-[3-(trifluoromethyl)phenyl]-ethylidene]-N-[4-(difluoromethoxy)phenyl]-hydrazinecarboxamide or M.22B.2: N-(3-Chloro-2-methylphenyl)-2-[(4-chlorophenyl)[4-[methyl(methylsulfonyl)amino]phenyl]methylene]-hydrazinecarboxamide;

M.23 Inhibitors of the of acetyl CoA carboxylase, such as Tetronic and Tetramic acid derivatives, for example spirodiclofen, spiromesifen or spirotetramat;

M.24 Mitochondrial complex IV electron transport inhibitors, for example M.24A phosphine such as aluminium phosphide, calcium phosphide, phosphine or zinc phosphide, or M.24B cyanide;

M.25 Mitochondrial complex II electron transport inhibitors, such as beta-ketonitrile derivatives, for example cyenopyrafen or cyflumetofen;

M.28 Ryanodine receptor-modulators from the class of diamides, as for example flubendiamide, chlorantraniliprole (rynaxypyr®), cyantraniliprole (cyazypyr®), tetraniliprole, or the phthalamide compounds M.28.1 : (R)-3-Chlor-N1 -{2-methyl-4-[1 ,2,2,2 -tetrafluor-1 -(trifluormethyl)ethyl]phenyl}-N2-(1 -methyl-2-methylsulfonylethyl)phthalamid and M.28.2: (S)-3-Chlor-N1 -{2-methyl-4-[1 ,2,2,2 -tetrafluor-1 -(trifluormethyl)ethyl]phenyl}-N2-(1 -methyl-2 -methylsulfonylethyl)phthalamid, or the compound M.28.3: 3-bromo-N-{2-bromo-4-chloro-6-[(1 -cyclopropylethyl)carbamoyl]phenyl}-1 -(3-ch lo rpy rid i n -2-y I )- 1 H-pyrazole-5-carboxamide (proposed ISO name: cyclaniliprole), or the compound M.28.4: methyl-2-[3,5-dibromo-2-({[3-bromo-1 -(3-ch lo rpy rid i n -2-y I )- 1 H-pyrazol-5-yl]carbonyl}amino)benzoyl]-1 ,2-dimethylhydrazinecarboxylate; or a compound selected from M.28.5a) to M.28.5d) and M.28.5h) to M.28.5I): M.28.5a) N-[4,6-dichloro-2-[(diethyl-lambda-4-sulfanylidene)-carbamoyl]-phenyl]-2-(3-chloro-2-pyridyl)-5-(trifluoromethyl)pyrazole-3-carboxamide;

M.28.5b) N-[4-chloro-2-[(diethyl-lambda-4-sulfanylidene)carbamoyl]-6-methyl-phenyl]-2-(3-chloro-2-pyridyl)-5-(trifluoromethyl)pyrazole-3-carboxamide; M.28.5c) N-[4-chloro-2-[(di-2-propyl-lambda-4-sulfanylidene)carbamoyl]-6-methyl-phenyl]-2-(3-chloro-2-pyridyl)-5-(trifluoromethyl)pyrazole-3-carboxamide; M.28.5d) N-[4,6-dichloro-2-[(di-2-propyl-lambda-4-sulfanylidene)carbamoyl]-phenyl]-2-(3-chloro-2-pyridyl)-5-(trifluoromethyl)pyrazole-3-carboxamide; M.28.5h) N-[4,6-dibromo-2-[(diethyl-lambda-4-sulfanylidene)carbamoyl]-phenyl]-2-(3-chloro-2-pyridyl)-5-(trifluoromethyl)pyrazole-3-carboxamide; M.28.5i) N-[2-(5-Amino-1 ,3,4-thiadiazol-2-yl)-4-chloro-6-methylphenyl]-3-bromo-1 -(3-chloro-2-pyridinyl)-1 H-pyrazole-5-carboxamide; M.28.5j) 3-Chloro-1 -(3-chloro-2-pyridinyl)-N-[2,4-dichloro-6-[[(1 -cyano-1 -methylethyl)amino]carbonyl]phenyl]-1 H-pyrazole-5-carboxamide; M.28.5k) 3-Bromo-N-[2,4-dichloro-6-(methylcarbamoyl)phenyl]-1 -(3,5-dichloro-2-pyridyl)-1 H-pyrazole-5-carboxamide; M.28.5I) N-[4-Chloro-2-[[(1 ,1 -dimethylethyl)amino]carbonyl]-6-methylphenyl]-1 -(3-chloro-2-pyridinyl)-3-(fluoromethoxy)-1 H-pyrazole-5-carboxamide; or

M.28.6: cyhalodiamide; or;

M.29. insecticidal active compounds of unknown or uncertain mode of action, as for example afidopyropen, afoxolaner, azadirachtin, amidoflumet, benzoximate, bifenazate, broflanilide, bromopropylate, chinomethionat, cryolite, dicloromezotiaz, dicofol, flufenerim, flometoquin, fluensulfone, fluhexafon, fluopyram, flupyradifurone, fluralaner, metoxadiazone,

piperonyl butoxide, pyflubumide, pyridalyl, pyrifluquinazon, sulfoxaflor, tioxazafen, triflumezopyrim, or the compounds

M.29.3: 1 1 -(4-chloro-2,6-dimethylphenyl)-12-hydroxy-1 , 4-dioxa-9-azadispiro[4.2.4.2]-tetradec-1 1 -en-10-one, or the compound

M.29.4: 3-(4’-fluoro-2,4-dimethylbiphenyl-3-yl)-4-hydroxy-8-oxa-1 -azaspiro[4.5]dec-3-en-2-one, or the compound

M.29.5: 1 -[2-fluoro-4-methyl-5-[(2,2,2-trifluoroethyl)sulfinyl]phenyl]-3-(trifluoromethyl)-1 H-1 ,2,4-triazole-5-amine, or actives on basis of bacillus firmus (Votivo, 1-1582); or

a compound selected from the of M.29.6, wherein the compound M.29.6a) to M.29.6k): M.29.6a) (E/Z)-N-[1 -[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-2,2,2-trifluoro-acetamide; M.29.6b) (E/Z)-N-[1 -[(6-chloro-5-fluoro-3-pyridyl)methyl]-2-pyridylidene]-2,2,2-trifluoro-acetamide; M.29.6c) (E/Z)-2,2,2-trifluoro-N-[1 -[(6-fluoro-3-pyridyl)methyl]-2-pyridylidene]acetamide; M.29.6d) (E/Z)-N-[1 -[(6-bromo-3-pyridyl)methyl]-2-pyridylidene]-2,2,2-trifluoro-acetamide; M.29.6e) (E/Z)-N-[1 -[1 -(6-chloro-3-pyridyl)ethyl]-2-pyridylidene]- 2.2.2-trifluoro-acetamide; M.29.6f) (E/Z)-N-[1 -[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-2,2-difluoro-acetamide; M.29.6g) (E/Z)-2-chloro-N-[1 -[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]- 2.2-difluoro-acetamide; M.29.6h) (E/Z)-N-[1 -[(2-chloropyrimidin-5-yl)methyl]-2-pyridylidene]- 2.2.2-trifluoro-acetamide; M.29.6i) (E/Z)-N-[1 -[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-2,2,3,3,3-pentafluoro-propanamide.); M.29.6j) N-[1 -[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-2,2,2-trifluoro-thioacetamide; or M.29.6k) N-[1 -[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-2,2,2-trifluoro-N'-isopropyl-acetamidine; or the compounds

M.29.8: fluazaindolizine; or the compounds

M.29.9.a): 4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4H-isoxazol-3-yl]-2-methyl-N-(1 -oxothietan-3-yl)benzamide; or M.29.9.b): fluxametamide; or

M.29.10: 5-[3-[2,6-dichloro-4-(3,3-dichloroallyloxy)phenoxy]propoxy]-1 H-pyrazole; or a compound selected from the of M.29.1 1 , wherein the compound M.29.1 1 b) to M.29.1 1 p): M.29.1 1 .b) 3-(benzoylmethylamino)-N-[2-bromo-4-[1 ,2,2,3,3,3-hexafluoro-1 -(trifluoromethyl)propyl]-6-(trifluoromethyl)phenyl]-2-fluoro-benzamide; M.29.1 1.c) 3-(benzoyl-methylamino)-2-fluoro-N-[2-iodo-4-[1 ,2,2,2-tetrafluoro-1 -(trifluoromethyl)ethyl]-6-(trifluoro-methyl)phenyl]-benzamide; M.29.1 1 .d) N-[3-[[[2-iodo-4-[1 ,2,2,2-tetrafluoro-1 -(trifluoromethyl)ethyl]-6-(trifluoromethyl)phenyl]amino]carbonyl]phenyl]-N-methyl-benzamide; M.29.1 1.e) N-[3-[[[2-bromo-4-[1 ,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]-6-(trifluoromethyl)phenyl]amino]carbonyl]-2-fluorophenyl]-4-fluoro-N-methyl-benzamide;

M.29.1 1.f) 4-fluoro-N-[2-fluoro-3-[[[2-iodo-4-[1 ,2,2,2-tetrafluoro-1 -(trifluoromethyl)ethyl]-6-(trifluoromethyl)phenyl]amino]carbonyl]phenyl]-N-methyl-benzamide; M.29.1 1 .g) 3-fluoro-N-[2-fluoro-3-[[[2-iodo-4-[1 ,2,2,2-tetrafluoro-1 -(trifluoromethyl)ethyl]-6-(trifluoro-methyl)phenyl]amino]carbonyl]phenyl]-N-methyl-benzamide; M.29.1 1 .h) 2-chloro-N-[3-[[[2-

iodo-4-[1 ,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]-6-(trifluoromethyl)phenyl]ami-no]carbonyl]phenyl]- 3-pyridinecarboxamide; M.29.1 1.i) 4-cyano-N-[2-cyano-5-[[2,6-dibromo-4-[1 ,2,2,3,3,3-hexafluoro-1-(trifluoromethyl)propyl]phenyl]carbamoyl]phenyl]-2-methyl-benzamide; M.29.1 1.j) 4-cyano-3-[(4-cyano-2-methyl-benzoyl)amino]-N-[2,6-dichloro-4-[1 ,2,2,3,3,3-hexafluoro-1-(trifluoromethyl)propyl]phenyl]-2-fluoro-benzamide; M.29.1 1.k) N-[5-[[2-chloro-6-cyano-4-[1 ,2,2,3,3,3-hexafluoro-1-(trifluoromethyl)propyl]phenyl]carbamoyl]-2-cyano-phenyl]-4-cyano-2-methyl-benzamide; M.29.1 1.1) N-[5-[[2-bromo-6-chloro-4-[2,2,2-trifluoro-1 -hydroxy-1 -(trifluoromethyl)ethyl]phenyl]carbamoyl]-2-cyano-phenyl]-4-cyano-2-methyl-benzamide; M.29.1 1.m) N-[5-[[2-bromo-6-chloro-4-[1 ,2,2,3,3,3-hexafluoro-1-(trifluoromethyl)propyl]phenyl]carbamoyl]-2-cyano-phenyl]-4-cyano-2-methyl-benzamide; M.29.11.n) 4-cyano-N-[2-cyano-5-[[2,6-dichloro-4-[1 ,2,2,3,3,3-hexafluoro-1-(trifluoromethyl)-propyl]phenyl]carbamoyl]phenyl]-2-methyl-benzamide; M.29.11.o) 4-cyano-N-[2-cyano-5-[[2,6-dichloro-4-[1 ,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl]carbamoyl]phenyl]-2-methyl-benzamide; M.29.11.p) N-[5-[[2-bromo-6-chloro-4-[1 ,2,2,2-tetrafluoro-1-(trifluoro-methyl)ethyl]phenyl]carbamoyl]-2-cyano-phenyl]-4-cyano-2-methyl-benzamide; or a compound selected from the of M.29.12, wherein the compound M.29.12a) to M.29.12m):

M.29.12.a) 2-(1 ,3-Dioxan-2-yl)-6-[2-(3-pyridinyl)-5-thiazolyl]-pyridine; M.29.12. b) 2-[6-[2-(5-Fluoro-3-pyridinyl)-5-thiazolyl]-2-pyridinyl]-pyrimidine; M.29.12. c) 2-[6-[2-(3-Pyridinyl)-5-thiazolyl]-2-pyridinyl]-pyrimidine; M.29.12. d) N-Methylsulfonyl-6-[2-(3-pyridyl)thiazol-5-yl]pyridine-2-carboxamide; M.29.12. e) N-Methylsulfonyl-6-[2-(3-pyridyl)thiazol-5-yl]pyridine-2-carboxamide; M.29.12.f) N-Ethyl-N-[4-methyl-2-(3-pyridyl)thiazol-5-yl]-3-methylthio-propanamide; M.29.12. g) N-Methyl-N-[4-methyl-2-(3-pyridyl)thiazol-5-yl]-3-methylthio-propanamide; M.29.12. h) N,2-Dimethyl-N-[4-methyl-2-(3-pyridyl)thiazol-5-yl]-3-methylthio-propanamide; M.29.12. i) N-Ethyl-2-methyl-N-[4-methyl-2-(3-pyridyl)thiazol-5-yl]-3-methylthio-propanamide; M.29.12.j) N-[4-Chloro-2-(3-pyridyl)thiazol-5-yl]-N-ethyl-2-methyl-3-methylthio-propanamide; M.29.12. k) N-[4-Chloro-2-(3-pyridyl)thiazol-5-yl]-N,2-dimethyl-3-methylthio-propanamide; M.29.12.1) N-[4-Chloro-2-(3-pyridyl)thiazol-5-yl]-N-methyl-3-methylthio-propanamide; M.29.12. m) N-[4-Chloro-2-(3-pyridyl)thiazol-5-yl]-N-ethyl-3-methylthio-propanamide; or the compounds

M.29.14a) 1-[(6-Chloro-3-pyridinyl)methyl]-1 ,2,3,5,6,7-hexahydro-5-methoxy-7-methyl-8-nitro-imidazo[1 ,2-a]pyridine; or M.29.14b) 1-[(6-Chloropyridin-3-yl)methyl]-7-methyl-8-nitro-1 ,2,3,5,6,7-hexahydroimidazo[1 ,2-a]pyridin-5-ol; or the compounds

M.29.16a) 1-isopropyl-N,5-dimethyl-N-pyridazin-4-yl-pyrazole-4-carboxamide; or M.29.16b) 1-(1 ,2-dimethylpropyl)-N-ethyl-5-methyl-N-pyridazin-4-yl-pyrazole-4-carboxamide; M.29.16c)

N,5-dimethyl-N-pyridazin-4-yl-1-(2,2,2-trifluoro-1-methyl-ethyl)pyrazole-4-carboxamide;

M.29.16d) 1-[1-(1-cyanocyclopropyl)ethyl]-N-ethyl-5-methyl-N-pyridazin-4-yl-pyrazole-4-carboxamide; M.29.16e) N-ethyl-1-(2-fluoro-1-methyl-propyl)-5-methyl-N-pyridazin-4-yl-

pyrazole-4-carboxamide; M.29.16f) 1-(1 ,2-dimethylpropyl)-N,5-dimethyl-N-pyridazin-4-yl-pyrazole-4-carboxamide; M.29.16g) 1 -[1 -(1 -cyanocyclopropyl)ethyl]-N,5-dimethyl-N-pyridazin-4-yl-pyrazole-4-carboxamide; M.29.16h) N-methyl-1-(2-fluoro-1-methyl-propyl]-5-methyl-N-pyridazin-4-yl-pyrazole-4-carboxamide; M.29.16i) 1-(4,4-difluorocyclohexyl)-N-ethyl-5-methyl-N-pyridazin-4-yl-pyrazole-4-carboxamide; or M.29.16j) 1-(4,4-difluoro-cyclohexyl)-N,5-dimethyl-N-pyridazin-4-yl-pyrazole-4-carboxamide, or

M.29.17 a compound selected from the compounds M.29.17a) to M.29.17j): M.29.17a) N-(1-methylethyl)-2-(3-pyridinyl)-2H-indazole-4-carboxamide; M.29.17b) N-cyclopropyl-2-(3-pyridinyl)-2H-indazole-4-carboxamide; M.29.17c) N-cyclohexyl-2-(3-pyridinyl)-2H-indazole-4-carboxamide; M.29.17d) 2-(3-pyridinyl)-N-(2,2,2-trifluoroethyl)-2H-indazole-4-carboxamide; M.29.17e) 2-(3-pyridinyl)-N-[(tetrahydro-2-furanyl)methyl]-2H-indazole-5-carboxamide;

M.29.17f) methyl 2-[[2-(3-pyridinyl)-2H-indazol-5-yl]carbonyl]hydrazinecarboxylate; M.29.17g) N-[(2,2-difluorocyclopropyl)methyl]-2-(3-pyridinyl)-2H-indazole-5-carboxamide; M.29.17h) N-(2,2-difluoropropyl)-2-(3-pyridinyl)-2H-indazole-5-carboxamide; M.29.17i) 2-(3-pyridinyl )-N-(2-pyrimidinylmethyl )-2H-indazole-5-carboxamide; M.29.17j) N-[(5-methyl-2-pyrazinyl)methyl]-2-(3-pyridinyl)-2H-indazole-5-carboxamide, or

M.29.18 a compound selected from the compounds M.29.18a) to M.29.18d): M.29.18a) N-[3-chloro-1-(3-pyridyl)pyrazol-4-yl]-N-ethyl-3-(3,3,3-trifluoropropylsulfanyl)propanamide;

M.29.18b) N-[3-chloro-1-(3-pyridyl)pyrazol-4-yl]-N-ethyl-3-(3,3,3-trifluoropropylsulfinyl)propanamide; M.29.18c) N-[3-chloro-1-(3-pyridyl)pyrazol-4-yl]-3-[(2,2-difluorocyclopropyl)methylsulfanyl]-N-ethyl-propanamide; M.29.18d) N-[3-chloro-1-(3-pyridyl)pyrazol-4-yl]-3-[(2,2-difluorocyclopropyl)methylsulfinyl]-N-ethyl-propanamide; or the compound

M.29.19 sarolaner, or the compound

M.29.20 lotilaner.

The commercially available compounds of the M listed above may be found in The

Pesticide Manual, 16th Edition, C. MacBean, British Crop Protection Council (2013) among other publications. The online Pesticide Manual is updated regularly and is accessible through http://bcpcdata.com/pesticide-manual.html.

Another online data base for pesticides providing the ISO common names is

http://www.alanwood.net/pesticides.

The M.4 neonicotinoid cycloxaprid is known from WO2010/069266 and WO201 1/069456, the neonicotinoid M.4A.2, sometimes also to be named as guadipyr, is known from

WO2013/003977, and the neonicotinoid M.4A.3 (approved as paichongding in China) is known from W02007/101369. The metaflumizone analogue M.22B.1 is described in

CN10171577 and the analogue M.22B.2 in CN102126994. The phthalamides M.28.1 and M.28.2 are both known from W02007/101540. The anthranilamide M.28.3 is described in

W02005/077934. The hydrazide compound M.28.4 is described in W02007/043677. The anthranilamides M.28.5a) to M.28.5d) and M.28.5h) are described in WO 2007/006670, WO2013/024009 and WO2013/024010, the anthranilamide M.28.5Ϊ) is described in

WO2011/085575, M.28.5j) in W02008/134969, M.28.5k) in US201 1/046186 and M.28.5I) in WO2012/034403. The diamide compound M.28.6 can be found in WO2012/034472. The spiroketal-substituted cyclic ketoenol derivative M.29.3 is known from W02006/089633 and the biphenyl-substituted spirocyclic ketoenol derivative M.29.4 from W02008/067911. The triazoylphenylsulfide M.29.5 is described in W02006/043635, and biological control agents on the basis of bacillus firmus are described in W02009/124707. The compounds M.29.6a) to M.29.6Ϊ) listed under M.29.6 are described in WO2012/029672, and M.29.6j) and M.29.6k) in WO2013/129688. The nematicide M.29.8 is known from WO2013/055584. The isoxazoline M.29.9.a) is described in WO2013/050317. The isoxazoline M.29.9.b) is described in WO2014/126208. The pyridalyl-type analogue M.29.10 is known from WO2010/060379. The carboxamides broflanilide and M.29.1 1.b) to M.29.1 1.h) are described in W02010/018714, and the carboxamides M.29.11 i) to M.29.1 1.p) in WO2010/127926. The pyridylthiazoles M.29.12. a) to M.29.12.C) are known from WO2010/006713, M.29.12.d) and M.29.12.e) are known from WO2012/000896, and M.29.12.f) to M.29.12.m) from WO2010/129497. The compounds M.29.14a) and M.29.14b) are known from W02007/101369. The pyrazoles M.29.16. a) to M.29.16h) are described in WO2010/034737, WO2012/084670, and

WO2012/143317, respectively, and the pyrazoles M.29.16i) and M.29.16j) are described in US 61/891437. The pyridinylindazoles M.29.17a) to M.29.17.j) are described in

WO2015/038503. The pyridylpyrazoles M.29.18a) to M.29.18d) are described in

US2014/0213448. The isoxazoline M.29.19 is described in WO2014/036056. The isoxazoline M.29.20 is known from WO2014/090918.

The following list of fungicides, in conjunction with which the compounds of the present invention can be used, is intended to illustrate the possible combinations but does not limit them:

A) Respiration inhibitors

Inhibitors of complex III at Q0 site (e. g. strobilurins): azoxystrobin (A.1.1 ), coumethoxy-strobin (A.1.2), coumoxystrobin (A.1.3), dimoxystrobin (A.1.4), enestroburin (A.1.5), fenaminstrobin (A.1.6), fenoxystrobin/flufenoxystrobin (A.1.7), fluoxastrobin (A.1.8), kresoxim-methyl (A.1.9), mandestrobin (A.1.10), metominostrobin (A.1.1 1 ), orysastrobin (A.1.12), picoxy.strobin (A.1.13), pyraclostrobin (A.1.14), pyrametostrobin (A.1.15), pyraoxystrobin (A.1.16), trifloxystrobin (A.1.17), 2-(2-(3-(2,6-dichlorophenyl)-1-methyl-allylideneaminooxymethyl)-phenyl)-2-methoxyimino-N-methyl-acetamide (A.1.18), pyribencarb (A.1.19), triclopyricarb/chlorodincarb (A.1.20), famoxadone (A.1.21 ), fenamidone (A.1.21 ), methyl-/V-[2-[(1 ,4-dimethyl-5-phenyl-pyrazol-3-yl)oxylmethyl]phenyl]-N-methoxy- carbamate (A.1.22), 1 -[3-chloro-2-[[1 -(4-chlorophenyl)-1 H-pyrazol-3-yl]oxymethyl]phenyl]-4-methyl-tetrazol-5-one (A.1.23), 1 -[3-bromo-2-[[1 -(4-chlorophenyl)pyrazol-3-yl]oxy-methyl]phenyl]-4-methyl-tetrazol-5-one (A.1.24), 1 -[2-[[1 -(4-chlorophenyl)pyrazol-3-yl]oxy-methyl]-3-methyl-phenyl]-4-methyl-tetrazol-5-one (A.1.25), 1 -[2-[[1 -(4-chlorophenyl)pyrazol-3-yl]oxymethyl]-3-fluoro-phenyl]-4-methyl-tetrazol-5-one (A.1.26), 1 -[2-[[1 -(2,4-dichloro-phenyl)pyrazol-3-yl]oxymethyl]-3-fluoro-phenyl]-4-methyl-tetrazol-5-one (A.1 .27), 1 -[2-[[4-(4-chlorophenyl)thiazol-2-yl]oxymethyl]-3-methyl-phenyl]-4-methyl-tetrazol-5-one (A.1.28), 1 -[3-chloro-2-[[4-(p-tolyl)thiazol-2-yl]oxymethyl]phenyl]-4-methyl-tetrazol-5-one (A.1 .29), 1 -[3-cyclopropyl-2-[[2-methyl-4-(1 -methylpyrazol-3-yl)phenoxy]methyl]phenyl]-4-methyl-tetrazol-5-one (A.1.30), 1 -[3-(difluoromethoxy)-2-[[2-methyl-4-(1 -methylpyrazol-3-yl)phenoxy]methyl]phenyl]-4-methyl-tetrazol-5-one (A.1.31 ), 1 -methyl-4-[3-methyl-2-[[2-methyl-4-(1 -methylpyrazol-3-yl)phenoxy]methyl]phenyl]tetrazol-5-one (A.1.32), 1 -me-thyl-4-[3-methyl-2-[[1 -[3-(trifluoromethyl)phenyl]-ethylideneamino]oxymethyl]phenyl]tetrazol-5-one (A.1.33), (Z,2E)-5-[1 -(2,4-dichlorophenyl)pyrazol-3-yl]oxy-2-methoxyimino-/V,3-dimethyl-pent-3-enamide (A.1 .34), (Z,2E)-5-[1 -(4-chlorophenyl)pyrazol-3-yl]oxy-2-methoxyimino-/V,3-dimethyl-pent-3-enamide (A.1.35), (Z,2E)-5-[1 -(4-chloro-2-fluoro-phenyl)pyrazol-3-yl]oxy-2-methoxyimino-/V,3-dimethyl-pent-3-enamide (A.1.36),

inhibitors of complex III at Q, site: cyazofamid (A.2.1 ), amisulbrom (A.2.2),

[(3S,6S,7R,8R)-8-benzyl-3-[(3-acetoxy-4-methoxy-pyridine-2-carbonyl)amino]-6-methyl-4,9-dioxo-1 ,5-dioxonan-7-yl] 2-methylpropanoate (A.2.3), [(3S,6S,7R,8R)-8-benzyl-3-[[3-(acet-oxymethoxy)-4-methoxy-pyridine-2-carbonyl]amino]-6-methyl-4,9-dioxo-1 ,5-dioxonan-7-yl] 2-methylpropanoate (A.2.4), [(3S,6S,7R,8R)-8-benzyl-3-[(3-isobutoxycarbonyloxy-4-meth-oxy-pyridine-2-carbonyl)amino]-6-methyl-4,9-dioxo-1 ,5-dioxonan-7-yl] 2-methylpropanoate (A.2.5), [(3S,6S,7R,8R)-8-benzyl-3-[[3-(1 ,3-benzodioxol-5-ylmethoxy)-4-methoxy-pyridine- 2-carbonyl]amino]-6-methyl-4,9-dioxo-1 ,5-dioxonan-7-yl] 2-methylpropanoate (A.2.6);

(3S,6S,7R,8R)-3-[[(3-hydroxy-4-methoxy-2-pyridinyl)carbonyl]amino]-6-methyl-4,9-dioxo-8-(phenylmethyl)-1 ,5-dioxonan-7-yl 2-methylpropanoate (A.2.7), (3S,6S,7R,8R)-8-benzyl- 3-[3-[(isobutyryloxy)methoxy]-4-methoxypicolinamido]-6-methyl-4,9-dioxo-1 ,5-dioxonan-7-yl isobutyrate (A.2.8);

inhibitors of complex II (e. g. carboxamides): benodanil (A.3.1 ), benzovindiflupyr (A.3.2), bixafen (A.3.3), boscalid (A.3.4), carboxin (A.3.5), fenfuram (A.3.6), fluopyram (A.3.7), flutolanil (A.3.8), fluxapyroxad (A.3.9), furametpyr (A.3.10), isofetamid (A.3.1 1 ), iso-pyrazam (A.3.12), mepronil (A.3.13), oxycarboxin (A.3.14), penflufen (A.3.14), penthiopyrad (A.3.15), sedaxane (A.3.16), tecloftalam (A.3.17), thifluzamide (A.3.18), N-(4'-trifluoromethylthiobiphenyl-2-yl)-3-difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxamide (A.3.19), N-(2-(1 ,3,3-trimethyl-butyl)-phenyl)-1 ,3-dimethyl-5-fluoro-1 H-pyrazole- 4-carboxamide (A.3.20), 3-(difluoromethyl)-1 -methyl-N-(1 ,1 ,3-trimethylindan-4-yl)pyrazole-4- carboxamide (A.3.21 ), 3-(trifluoromethyl)-1 -methyl-N-(1 ,1 ,3-trimethylindan-4-yl)pyrazole-4-carboxamide (A.3.22), 1 ,3-dimethyl-N-(1 ,1 ,3-trimethylindan-4-yl)pyrazole-4-carboxamide (A.3.23), 3-(trifluoromethyl)-1 ,5-dimethyl-N-(1 ,1 ,3-trimethylindan-4-yl)pyrazole-4-carboxamide (A.3.24), 1 ,3,5-trimethyl-N-(1 ,1 ,3-trimethylindan-4-yl)pyrazole-4-carboxamide (A.3.25), N-(7-fluoro-1 ,1 ,3-trimethyl-indan-4-yl)-1 ,3-dimethyl-pyrazole-4-carboxamide (A.3.26), N-[2-(2,4-dichlorophenyl)-2-methoxy-1 -methyl-ethyl]-3-(difluoromethyl)-1 -methyl-pyrazole-4-carboxamide (A.3.27);

other respiration inhibitors (e. g. complex I, uncouplers): diflumetorim (A.4.1 ), (5,8-difluoroquinazolin-4-yl)-{2-[2-fluoro-4-(4-trifluoromethylpyridin-2-yloxy)-phenyl]-ethyl}-amine (A.4.2); nitrophenyl derivates: binapacryl (A.4.3), dinobuton (A.4.4), dinocap (A.4.5), fluazinam (A.4.6); ferimzone (A.4.7); organometal compounds: fentin salts, such as fentin-acetate (A.4.8), fentin chloride (A.4.9) or fentin hydroxide (A.4.10); ametoctradin (A.4.1 1 ); and silthiofam (A.4.12);

B) Sterol biosynthesis inhibitors (SBI fungicides)

C14 demethylase inhibitors (DMI fungicides): triazoles: azaconazole (B.1 .1 ), bitertanol (B.1.2), bromuconazole (B.1.3), cyproconazole (B.1 .4), difenoconazole (B.1 .5), diniconazole (B.1.6), diniconazole-M (B.1 .7), epoxiconazole (B.1.8), fenbuconazole (B.1 .9),

fluquinconazole (B.1.10), flusilazole (B.1.1 1 ), flutriafol (B.1.12), hexaconazole (B.1.13), imibenconazole (B.1.14), ipconazole (B.1 .15), metconazole (B.1.17), myclobutanil (B.1.18), oxpoconazole (B.1.19), paclobutrazole (B.1 .20), penconazole (B.1 .21 ), propiconazole (B.1.22), prothioconazole (B.1 .23), simeconazole (B.1 .24), tebuconazole (B.1 .25), tetraconazole (B.1.26), triadimefon (B.1 .27), triadimenol (B.1 .28), triticonazole (B.1.29), uniconazole (B.1 .30), 1 -[re/-(2S;3R)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl)-oxiranylmethyl]-5-thiocyanato-1 H-[1 ,2,4]triazolo (B.1 .31 ), 2-[re/-(2S;3R)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl)-oxiranylmethyl]-2H-[1 ,2,4]triazole-3-thiol (B.1 .32), 2-[2-chloro-4-(4-chlorophenoxy)phenyl]-1 -(1 ,2,4-triazol-1 -yl)pentan-2-ol (B.1 .33), 1 -[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1 -cyclopropyl-2-(1 ,2,4-triazol-1 -yl)ethanol (B.1 .34), 2-[4-(4-chloro-phenoxy)-2-(trifluoromethyl)phenyl]-1 -(1 ,2,4-triazol-1 -yl)butan-2-ol (B.1.35), 2-[2-chloro-4-(4-chlorophenoxy)phenyl]-1 -(1 ,2,4-triazol-1 -yl)butan-2-ol (B.1 .36), 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-3-methyl-1 -(1 ,2,4-triazol-1-yl)butan-2-ol (B.1 .37), 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1 -(1 ,2,4-triazol-1 -yl)propan-2-ol (B.1 .38), 2-[2-chloro-4-(4-chlorophenoxy)phenyl]-3-methyl-1 -(1 ,2,4-triazol-1 -yl)butan-2-ol (B.1 .39), 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1 -(1 ,2,4-triazol-1 -yl)pentan-2-ol (B.1.40), 2-[4-(4-fluorophenoxy)-2-(trifluoromethyl)phenyl]-1 -(1 ,2,4-triazol-1 -yl)propan-2-ol (B.1 .41 ), 2-[2-chloro-4-(4-chlorophenoxy)phenyl]-1 -(1 ,2,4-triazol-1 -yl)pent-3-yn-2-ol (B.1 .51 ); imidazoles: imazalil (B.1 .42), pefurazoate (B.1 .43), prochloraz (B.1.44), triflumizol (B.1 .45); pyrimidines, pyridines and piperazines: fenarimol (B.1 .46), nuarimol (B.1 .47), pyrifenox (B.1 .48), triforine (B.1.49), [3-(4-chloro-2-fluoro-phenyl)-5-(2,4-difluorophenyl)isoxazol-4-yl]-(3-pyridyl)methanol (B.1.50);

Deltal 4-reductase inhibitors: aldimorph (B.2.1 ), dodemorph (B.2.2), dodemorph-acetate (B.2.3), fenpropimorph (B.2.4), tridemorph (B.2.5), fenpropidin (B.2.6), piperalin (B.2.7), spiroxamine (B.2.8);

Inhibitors of 3-keto reductase: fenhexamid (B.3.1 );

C) Nucleic acid synthesis inhibitors

phenylamides or acyl amino acid fungicides: benalaxyl (C.1.1 ), benalaxyl-M (C.1.2), kiralaxyl (C.1.3), metalaxyl (C.1.4), metalaxyl-M (mefenoxam, C.1.5), ofurace (C.1.6), oxadixyl (C.1.7);

others: hymexazole (C.2.1 ), octhilinone (C.2.2), oxolinic acid (C.2.3), bupirimate (C.2.4), 5-fluorocytosine (C.2.5), 5-fluoro-2-(p-tolylmethoxy)pyrimidin-4-amine (C.2.6), 5-fluoro-2-(4-fluorophenylmethoxy)pyrimidin-4-amine (C.2.7);

D) Inhibitors of cell division and cytoskeleton

tubulin inhibitors, such as benzimidazoles, thiophanates: benomyl (D1.1 ), carbendazim (D1.2), fuberidazole (D1.3), thiabendazole (D1.4), thiophanate-methyl (D1.5);

triazolopyrimidines: 5-chloro-7-(4-methylpiperidin-1-yl)-6-(2,4,6-trifluorophenyl)-[1 ,2,4]tri-azolo[1 ,5-a]pyrimidine (D1.6);

other cell division inhibitors: diethofencarb (D2.1 ), ethaboxam (D2.2), pencycuron (D2.3), fluopicolide (D2.4), zoxamide (D2.5), metrafenone (D2.6), pyriofenone (D2.7);

E) Inhibitors of amino acid and protein synthesis

methionine synthesis inhibitors (anilino-pyrimidines): cyprodinil (E.1.1 ), mepanipyrim (E.1.2), pyrimethanil (E.1.3);

protein synthesis inhibitors: blasticidin-S (E.2.1 ), kasugamycin (E.2.2), kasugamycin hydrochloride-hydrate (E.2.3), mildiomycin (E.2.4), streptomycin (E.2.5), oxytetracyclin (E.2.6), polyoxine (E.2.7), validamycin A (E.2.8);

F) Signal transduction inhibitors

MAP / histidine kinase inhibitors: fluoroimid (F.1.1 ), iprodione (F.1.2), procymidone (F.1.3), vinclozolin (F.1.4), fenpiclonil (F.1.5), fludioxonil (F.1.6);

G protein inhibitors: quinoxyfen (F.2.1 );

G) Lipid and membrane synthesis inhibitors

Phospholipid biosynthesis inhibitors: edifenphos (G.1.1 ), iprobenfos (G.1.2), pyrazo-phos (G.1.3), isoprothiolane (G.1.4);

lipid peroxidation: dicloran (G.2.1 ), quintozene (G.2.2), tecnazene (G.2.3), tolclofos-methyl (G.2.4), biphenyl (G.2.5), chloroneb (G.2.6), etridiazole (G.2.7);

phospholipid biosynthesis and cell wall deposition: dimethomorph (G.3.1 ), flumorph (G.3.2), mandipropamid (G.3.3), pyrimorph (G.3.4), benthiavalicarb (G.3.5), iprovalicarb

(G.3.6), valifenalate (G.3.7) and N-(1 -(1 -(4-cyano-phenyl)ethanesulfonyl)-but-2-yl) carbamic acid-(4-fluorophenyl) ester (G.3.8);

compounds affecting cell membrane permeability and fatty acides: propamocarb (G.4.1 );

fatty acid amide hydrolase inhibitors: oxathiapiprolin (G.5.1 ), 2-{3-[2-(1 -{[3,5-bis(di-fluoromethyl-1 H-pyrazol-1 -yl]acetyl}piperidin-4-yl)-1 ,3-thiazol-4-yl]-4,5-dihydro-1 ,2-oxazol-5-yljphenyl methanesulfonate (G.5.2), 2-{3-[2-(1 -{[3, 5-bis(difluoromethyl)-1 H-pyrazol-1 -yl]acetyl}piperidin-4-yl) 1 ,3-thiazol-4-yl]-4,5-dihydro-1 ,2-oxazol-5-yl}-3-chlorophenyl methanesulfonate (G.5.3);

H) Inhibitors with Multi Site Action

inorganic active substances: Bordeaux mixture (H.1.1 ), copper acetate (H.1 .2), copper hydroxide (H.1.3), copper oxychloride (H.1 .4), basic copper sulfate (H.1 .5), sulfur (H.1.6); thio- and dithiocarbamates: ferbam (H.2.1 ), mancozeb (H.2.2), maneb (H.2.3), metam (H.2.4), metiram (H.2.5), propineb (H.2.6), thiram (H.2.7), zineb (H.2.8), ziram (H.2.9);

organochlorine compounds (e. g. phthalimides, sulfamides, chloronitriles): anilazine (H.3.1 ), chlorothalonil (H.3.2), captafol (H.3.3), captan (H.3.4), folpet (H.3.5), dichlofluanid (H.3.6), dichlorophen (H.3.7), hexachlorobenzene (H.3.8), pentachlorphenole (H.3.9) and its salts, phthalide (H.3.10), tolylfluanid (H.3.1 1 ), N-(4-chloro-2-nitro-phenyl)-N-ethyl-4-methyl-benzenesulfonamide (H.3.12);

guanidines and others: guanidine (H.4.1 ), dodine (H.4.2), dodine free base (H.4.3), guazatine (H.4.4), guazatine-acetate (H.4.5), iminoctadine (H.4.6), iminoctadine-triacetate (H.4.7), iminoctadine-tris(albesilate) (H.4.8), dithianon (H.4.9), 2,6-dimethyl-1 H,5H-[1 ,4]dithiino[2,3-c:5,6-c']dipyrrole-1 ,3,5,7(2H,6H)-tetraone (H.4.10);

I) Cell wall synthesis inhibitors

inhibitors of glucan synthesis: validamycin (1.1.1 ), polyoxin B (1.1 .2);

melanin synthesis inhibitors: pyroquilon (1.2.1 ), tricyclazole (1.2.2), carpropamid (I.2.3), dicyclomet (I.2.4), fenoxanil (1.2.5);

J) Plant defence inducers

acibenzolar-S-methyl (J.1.1 ), probenazole (J.1.2), isotianil (J.1 .3), tiadinil (J.1 .4), prohexadione-calcium (J.1.5); phosphonates: fosetyl (J.1 .6), fosetyl-aluminum (J.1 .7), phosphorous acid and its salts (J.1.8), potassium or sodium bicarbonate (J.1 .9);

K) Unknown mode of action

bronopol (K.1 .1 ), chinomethionat (K.1.2), cyflufenamid (K.1.3), cymoxanil (K.1 .4), dazomet (K.1.5), debacarb (K.1 .6), diclomezine (K.1.7), difenzoquat (K.1 .8), difenzoquat-methylsulfate (K.1 .9), diphenylamin (K.1 .10), fenpyrazamine (K.1 .1 1 ), flumetover (K.1.12), flusulfamide (K.1 .13), flutianil (K.1.14), methasulfocarb (K.1 .15), nitrapyrin (K.1 .16), nitrothal-isopropyl (K.1 .18), oxathiapiprolin (K.1 .19), tolprocarb (K.1 .20), oxin-copper (K.1 .21 ),

proquinazid (K.1.22), tebufloquin (K.1.23), tecloftalam (K.1 .24), triazoxide (K.1 .25), 2-butoxy-6-iodo-3-propylchromen-4-one (K.1.26), 2-[3,5-bis(difluoromethyl)-1 H-pyrazol-1 -yl]-1 -[4-(4-{5-[2-(prop-2-yn-1 -yloxy)phenyl]-4,5-dihydro-1 ,2-oxazol-3-yl}-1 ,3-thiazol-2-yl)piperidin-1 -yl]etha-none (K.1.27), 2-[3,5-bis(difluoromethyl)-1 H-pyrazol-1 -yl]-1 -[4-(4-{5-[2-fluoro-6-(prop-2-yn-1 -yloxy)phenyl]-4,5-dihydro-1 ,2-oxazol-3-yl}-1 ,3-thiazol-2-yl)piperidin-1 -yl]ethanone (K.1.28),

2-[3,5-bis(difluoromethyl)-1 H-pyrazol-1 -yl]-1 -[4-(4-{5-[2-chloro-6-(prop-2-yn-1 -yloxy)phenyl]-4,5-dihydro-1 ,2-oxazol-3-yl}-1 ,3-thiazol-2-yl)piperidin-1 -yl]ethanone (K.1 .29), N-(cyclo-propylmethoxyimino-(6-difluoro-methoxy-2,3-difluoro-phenyl)-methyl)-2-phenyl acetamide (K.1.30), N'-(4-(4-chloro-3-trifluoromethyl-phenoxy)-2,5-dimethyl-phenyl)-N-ethyl-N-methyl formamidine (K.1.31 ), N'-(4-(4-fluoro-3-trifluoromethyl-phenoxy)-2,5-dimethyl-phenyl)-N-ethyl-N-methyl formamidine (K.1 .32), N'-(2-methyl-5-trifluoromethyl-4-(3-trimethylsilanyl-prop-oxy)-phenyl)-N-ethyl-N-methyl formamidine (K.1 .33), N'-(5-difluoromethyl-2-methyl-4-(3-tri-methylsilanyl-propoxy)-phenyl)-N-ethyl-N-methyl formamidine (K.1.34), methoxy-acetic acid 6-tert-butyl-8-fluoro-2,3-dimethyl-quinolin-4-yl ester (K.1 .35), 3-[5-(4-methylphenyl)-2,3-dimethyl-isoxazolidin-3-yl]-pyridine (K.1 .36), 3-[5-(4-chloro-phenyl)-2,3-dimethyl-isoxazolidin- 3-yl]-pyridine (pyrisoxazole) (K.1 .37), N-(6-methoxy-pyridin-3-yl) cyclopropanecarboxylic acid amide (K.1.38), 5-chloro-1 -(4,6-dimethoxy-pyrimidin-2-yl)-2-methyl-1 H-benzoimidazole (K.1.39), 2-(4-chloro-phenyl)-N-[4-(3,4-dimethoxy-phenyl)-isoxazol-5-yl]-2-prop-2-ynyloxy-acetamide, ethyl (Z)-3-amino-2-cyano-3-phenyl-prop-2-enoate (K.1.40), picarbutrazox

(K.1.41 ), pentyl N-[6-[[(Z)-[(1 -methyltetrazol-5-yl)-phenyl-methylene]amino]oxymethyl]-2-pyridyl]carbamate (K.1 .42), 2-[2-[(7,8-difluoro-2-methyl-3-quinolyl)oxy]-6-fluoro-phenyl]propan-2-ol (K.1 .43), 2-[2-fluoro-6-[(8-fluoro-2-methyl-3-quinolyl)oxy]phen-yl]propan-2-ol (K.1 .44), 3-(5-fluoro-3,3,4,4-tetramethyl-3,4-dihydroisoquinolin-1 -yl)quinoline (K.1 .45), 3-(4,4-difluoro-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl)quinoline (K.1 .46), 3-(4,4,5-trifluoro-3,3-dimethyl-3,4-dihydroisoquinolin-1 -yl)quinoline (K.1 .47), 9-fluoro-2,2-dimethyl-5-(3-quinolyl)-3H-1 ,4-benzoxazepine (K.1 .48).

The fungicides described by common names, their preparation and their activity e.g.

against harmful fungi is known (cf.: http://www.alanwood.net/pesticides/); these substances are commercially available.

The fungicides described by lUPAC nomenclature, their preparation and their pesticidal activity is also known (cf. Can. J. Plant Sci. 48(6), 587-94, 1968; EP-A 141 317; EP-A 152 031 ; EP-A 226 917; EP-A 243 970; EP-A 256 503; EP-A 428 941 ; EP-A 532 022; EP-A 1 028 125; EP-A 1 035 122; EP-A 1 201 648; EP-A 1 122 244, JP 2002316902; DE 19650197; DE 10021412; DE 102005009458; US 3,296,272; US 3,325,503; WO 98/46608;

WO 99/14187; WO 99/24413; WO 99/27783; WO 00/29404; WO 00/46148; WO 00/65913;

WO 01/54501 ; WO 01/56358; WO 02/22583; WO 02/40431 ; WO 03/10149; WO 03/1 1853;

WO 03/14103; WO 03/16286; WO 03/53145; WO 03/61388; WO 03/66609; WO 03/74491 ;

WO 04/49804; WO 04/83193; WO 05/120234; WO 05/123689; WO 05/123690;

WO 05/63721 ; WO 05/87772; WO 05/87773; WO 06/15866; WO 06/87325; WO 06/87343; WO 07/82098; WO 07/90624, WO 11/028657, WO2012/168188, WO 2007/006670, WO 201 1/77514; W013/047749, WO 10/069882, WO 13/047441 , WO 03/16303, WO 09/90181 , WO 13/007767, WO 13/010862, WO 13/127704, WO 13/024009, WO 13/024010 and WO 13/047441 , WO 13/162072, WO 13/092224, WO 1 1/135833).

Biopesticides

Suitable mixing partners for the compounds of the present invention also include biopesticides.

Biopesticides have been defined as a form of pesticides based on micro-organisms (bacteria, fungi, viruses, nematodes, etc.) or natural products (compounds, such as metabolites, proteins, or extracts from biological or other natural sources) (U.S.

Environmental Protection Agency: http://www.epa.gov/pesticides/biopesticides/).

Biopesticides fall into two major classes, microbial and biochemical pesticides:

(1 ) Microbial pesticides consist of bacteria, fungi or viruses (and often include the metabolites that bacteria and fungi produce). Entomopathogenic nematodes are also classified as microbial pesticides, even though they are multi-cellular.

(2) Biochemical pesticides are naturally occurring substances or or structurally-similar and functionally identical to a naturally-occurring substance and extracts from biological sources that control pests or provide other crop protection uses as defined below, but have non-toxic mode of actions (such as growth or developmental regulation, attractents, repellents or defence activators (e.g. induced resistance) and are relatively non-toxic to mammals.

Biopesticides for use against crop diseases have already established themselves on a variety of crops. For example, biopesticides already play an important role in controlling downy mildew diseases. Their benefits include: a 0-Day Pre-Harvest Interval, the ability to use under moderate to severe disease pressure, and the ability to use in mixture or in a rotational program with other registered pesticides.

A major growth area for biopesticides is in the area of seed treatments and soil

amendments. Biopesticidal seed treatments are e.g. used to control soil borne fungal pathogens that cause seed rots, damping-off, root rot and seedling blights. They can also be used to control internal seed borne fungal pathogens as well as fungal pathogens that are on the surface of the seed. Many biopesticidal products also show capacities to stimulate plant host defenses and other physiological processes that can make treated crops more resistant to a variety of biotic and abiotic stresses or can regulate plant growth. Many biopesticidal products also show capacities to stimulate plant health, plant growth and/or yield enhancing activity.

The following list of biopesticides, in conjunction with which the compounds of the present invention can be used, is intended to illustrate the possible combinations but does not limit them:

L) Biopesticides

L1 ) Microbial pesticides with fungicidal, bactericidal, viricidal and/or plant defense activator activity: Ampelomyces quisqualis, Aspergillus flavus, Aureobasidium pullulans, Bacillus altitudinis, B. amyloliquefaciens, B. megaterium, B. mojavensis, B. mycoides, B. pumilus, B. simplex, B. solisalsi, B. subtilis, B. subtilis var. amyloliquefaciens, Candida oleophila, C. saitoana, Clavibacter michiganensis (bacteriophages), Coniothyrium minitans, Cryphonectria parasitica, Cryptococcus albidus, Dilophosphora alopecuri, Fusarium oxysporum,

Clonostachys rosea f. catenulate (also named Gliocladium catenulatum), Gliocladium roseum, Lysobacter antibioticus, L. enzymogenes, Metschnikowia fructicola, Microdochium dimerum, Microsphaeropsis ochracea, Muscodor albus, Paenibacillus alvei, Paenibacillus polymyxa, Pantoea vagans, Penicillium bilaiae, Phlebiopsis gigantea, Pseudomonas sp., Pseudomonas chloraphis, Pseudozyma flocculosa, Pichia anomala, Pythium oligandrum, Sphaerodes mycoparasitica, Streptomyces griseoviridis, S. lydicus, S. violaceusniger, Talaromyces flavus, Trichoderma asperelloides, T. asperellum, T. atroviride, T. fertile, T. gamsii, T. harmatum, T. harzianum, T. polysporum, T. stromaticum, T. virens, T. viride, Typhula phacorrhiza, Ulocladium oudemansii, Verticillium dahlia, zucchini yellow mosaic virus (avirulent strain);

L2) Biochemical pesticides with fungicidal, bactericidal, viricidal and/or plant defense activator activity: harpin protein, Reynoutria sachalinensis extract;

L3) Microbial pesticides with insecticidal, acaricidal, molluscidal and/or nematicidal activity: Agrobacterium radiobacter, Bacillus cereus, B. firmus, B. thuringiensis, B. thuringiensis ssp. aizawai, B. t. ssp. israelensis, B. t. ssp. galleriae, B. t. ssp. kurstaki, B. t. ssp. tenebrionis, Beauveria bassiana, B. brongniartii, Burkholderia spp., Chromobacterium subtsugae, Cydia pomonella granulovirus (CpGV), Cryptophlebia leucotreta granulovirus (CrleGV),

Flavobacterium spp., Helicoverpa armigera nucleopolyhedrovirus (HearNPV), Helicoverpa zea nucleopolyhedrovirus (HzNPV), Helicoverpa zea single capsid nucleopolyhedrovirus (HzSNPV), Heterorhabditis bacteriophora, Isaria fumosorosea, Lecanicillium longisporum, L. muscarium, Metarhizium anisopliae, Metarhizium anisopliae var. anisopliae, M. anisopliae var. acridum, Nomuraea rileyi, Paecilomyces fumosoroseus, P. lilacinus, Paenibacillus popilliae, Pasteuria spp., P. nishizawae, P. penetrans, P. ramosa, P. thornea, P. usgae, Pseudomonas fluorescens, Spodoptera littoralis nucleopolyhedrovirus (SpliNPV),

Steinernema carpocapsae, S. feltiae, S. kraussei, Streptomyces galbus, S. microflavus,

L4) Biochemical pesticides with insecticidal, acaricidal, molluscidal, pheromone and/or nematicidal activity: L-carvone, citral, (E,Z)-7,9-dodecadien-1-yl acetate, ethyl formate, (E,Z)-2, 4-ethyl decadienoate (pear ester), (Z,Z,E)-7,1 1 ,13-hexadecatrienal, heptyl butyrate,

isopropyl myristate, lavanulyl senecioate, cis-jasmone, 2-methyl 1 -butanol, methyl eugenol, methyl jasmonate, (E,Z)-2,13-octadecadien-1-ol, (E,Z)-2,13-octadecadien-1-ol acetate, (E,Z)-3,13-octadecadien-1-ol, R-1-octen-3-ol, pentatermanone, (E,Z,Z)-3,8,11-tetradecatrienyl acetate, (Z,E)-9,12-tetradecadien-1-yl acetate, Z-7-tetradecen-2-one, Z-9-tetradecen-1-yl acetate, Z-11-tetradecenal, Z-11-tetradecen-1-ol, extract of Chenopodium ambrosiodes, Neem oil, Quillay extract;

L5) Microbial pesticides with plant stress reducing, plant growth regulator, plant growth promoting and/or yield enhancing activity: Azospirillum amazonense, A. brasilense, A.

lipoferum, A. irakense, A. halopraeferens, Bradyrhizobium spp., B. elkanii, B. japonicum, B. liaoningense, B. iupini, Delftia acidovorans, Glomus intraradices, Mesorhizobium spp., Rhizobium leguminosarum bv. phaseoli, R. I. bv. trifolii, R. I. bv. viciae, R. tropici,

Sinorhizobium meliloti.

The biopesticides from L1 ) and/or L2) may also have insecticidal, acaricidal, molluscidal, pheromone, nematicidal, plant stress reducing, plant growth regulator, plant growth promoting and/or yield enhancing activity. The biopesticides from L3) and/or L4) may also have fungicidal, bactericidal, viricidal, plant defense activator, plant stress reducing, plant growth regulator, plant growth promoting and/or yield enhancing activity. The biopesticides from L5) may also have fungicidal, bactericidal, viricidal, plant defense activator, insecticidal, acaricidal, molluscidal, pheromone and/or nematicidal activity.

Many of these biopesticides have been deposited under deposition numbers mentioned herein (the prefices such as ATCC or DSM refer to the acronym of the respective culture collection, for details see e. g. here: http://www. wfcc.info/ccinfo/collection/bv acronym/), are referred to in literature, registered and/or are commercially available: mixtures of

Aureobasidium pullulans DSM 14940 and DSM 14941 isolated in 1989 in Konstanz,

Germany (e. g. blastospores in Blossom Protect® from bio-ferm GmbH, Austria), Azospirillum brasilense Sp245 originally isolated in wheat reagion of South Brazil (Passo Fundo) at least prior to 1980 (BR 11005; e. g. GELFIX® Gramineas from BASF Agricultural Specialties Ltd., Brazil), A. brasilense strains Ab-V5 and Ab-V6 (e. g. in AzoMax from Novozymes BioAg Produtos papra Agricultura Ltda., Quattro Barras, Brazil or Simbiose-Maiz® from Simbiose-Agro, Brazil; Plant Soil 331 , 413-425, 2010), Bacillus amyloliquefaciens strain AP-188 (NRRL B-50615 and B-50331 ; US 8,445,255); B. amyloliquefaciens spp. plantarum D747 isolated from air in Kikugawa-shi, Japan (US 20130236522 A1 ; FERM BP-8234; e. g. Double

Nickel™ 55 WDG from Certis LLC, USA), B. amyloliquefaciens spp. plantarum FZB24 isolated from soil in Brandenburg, Germany (also called SB3615; DSM 96-2; J. Plant Dis. Prot. 105, 181-197, 1998; e. g. Taegro® from Novozyme Biologicals, Inc., USA), B.

amyloliquefaciens ssp. plantarum FZB42 isolated from soil in Brandenburg, Germany (DSM 231 17; J. Plant Dis. Prot. 105, 181-197, 1998; e. g. RhizoVital® 42 from AbiTEP GmbH,

Germany), B. amyloliquefaciens ssp. plantarum MBI600 isolated from faba bean in Sutton Bonington, Nottinghamshire, U.K. at least before 1988 (also called 1430; NRRL B-50595;

US 2012/0149571 A1 ; e. g. Integral® from BASF Corp., USA), B. amyloliquefaciens spp. plantarum QST-713 isolated from peach orchard in 1995 in California, U.S.A. (NRRL B-21661 ; e. g. Serenade® MAX from Bayer Crop Science LP, USA), B. amyloliquefaciens spp. plantarum TJ1000 isolated in 1992 in South Dakoda, U.S.A. (also called 1 BE; ATCC BAA-390; CA 2471555 A1 ; e. g. QuickRoots™ from TJ Technologies, Watertown, SD, USA), B. firmus CNCM 1-1582, a variant of parental strain EIP-N1 (CNCM 1-1556) isolated from soil of central plain area of Israel (WO 2009/126473, US 6,406,690; e. g. Votivo® from Bayer CropScience LP, USA), B. pumilus GHA 180 isolated from apple tree rhizosphere in Mexico (IDAC 260707-01 ; e. g. PRO-MIX® BX from Premier Horticulture, Quebec, Canada), B. pumilus INR-7 otherwise referred to as BU-F22 and BU-F33 isolated at least before 1993 from cucumber infested by Erwinia tracheiphila (NRRL B-50185, NRRL B-50153; US

8,445,255), B. pumilus QST 2808 was isolated from soil collected in Pohnpei, Federated States of Micronesia, in 1998 (NRRL B-30087; e. g. Sonata® or Ballad® Plus from Bayer Crop Science LP, USA), B. simplex ABU 288 (NRRL B-50304; US 8,445,255), B. subtilis FB17 also called UD 1022 or UD10-22 isolated from red beet roots in North America (ATCC PTA-11857; System. Appl. Microbiol. 27, 372-379, 2004; US 2010/0260735;

WO 201 1/109395); B. thuringiensis ssp. aizawai ABTS-1857 isolated from soil taken from a lawn in Ephraim, Wisconsin, U.S.A., in 1987 (also called ABG-6346; ATCC SD-1372; e. g. XenTari® from BioFa AG, Munsingen, Germany), B. t. ssp. ku rsta ki ABTS-351 identical to HD-1 isolated in 1967 from diseased Pink Bollworm black larvae in Brownsville, Texas, U.S.A. (ATCC SD-1275; e. g. Dipel® DF from Valent BioSciences, IL, USA), B. t. ssp.

tenebrionis NB-176-1 , a mutant of strain NB-125, a wild type strain isolated in 1982 from a dead pupa of the beetle Tenebrio molitor (DSM 5480; EP 585 215 B1 ; e. g. Novodor® from Valent BioSciences, Switzerland), Beauveria bassiana GHA (ATCC 74250; e. g.

BotaniGard® 22WGP from Laverlam Int. Corp., USA), B. bassiana JW-1 (ATCC 74040; e. g. Naturalis® from CBC (Europe) S.r.l., Italy), Bradyrhizobium elkanii strains SEMIA 5019 (also called 29W) isolated in Rio de Janeiro, Brazil and SEMIA 587 isolated in 1967 in the State of Rio Grande do Sul, from an area previously inoculated with a North American isolate, and used in commercial inoculants since 1968 (Appl. Environ. Microbiol. 73(8), 2635, 2007; e. g. GELFIX 5 from BASF Agricultural Specialties Ltd., Brazil), B. japonicum 532c isolated from Wisconsin field in U.S.A. (Nitragin 61A152; Can. J. Plant. Sci. 70, 661-666, 1990; e. g. in Rhizoflo®, Histick®, Hicoat® Super from BASF Agricultural Specialties Ltd., Canada), B. japonicum E-109 variant of strain USDA 138 (INTA E109, SEMIA 5085; Eur. J. Soil Biol. 45, 28-35, 2009; Biol. Fertil. Soils 47, 81-89, 2011 ); B. japonicum strains deposited at SEMIA known from Appl. Environ. Microbiol. 73(8), 2635, 2007: SEMIA 5079 isolated from soil in Cerrados region, Brazil by Embrapa-Cerrados used in commercial inoculants since 1992 (CPAC 15; e. g. GELFIX 5 or ADHERE 60 from BASF Agricultural Specialties Ltd., Brazil), B. japonicum SEMIA 5080 obtained under lab condtions by Embrapa-Cerrados in Brazil and used in commercial inoculants since 1992, being a natural variant of SEMIA 586 (CB1809) originally isolated in U.S.A. (CPAC 7; e. g. GELFIX 5 or ADHERE 60 from BASF Agricultural Specialties Ltd., Brazil); Burkholderia sp. A396 isolated from soil in Nikko, Japan, in 2008 (NRRL B-50319; WO 2013/032693; Marrone Bio Innovations, Inc., USA), Coniothyrium minitans CON/M/91-08 isolated from oilseed rape (WO 1996/021358; DSM 9660; e. g.

Contans® WG, Intercept® WG from Bayer CropScience AG, Germany), harpin (alpha-beta) protein (Science 257, 85-88, 1992; e. g. Messenger™ or HARP-N-Tek from Plant Health Care pic, U.K.), Helicoverpa armigera nucleopolyhedrovirus (HearNPV) (J. Invertebrate Pathol. 107, 112-126, 2011 ; e. g. Helicovex® from Adermatt Biocontrol, Switzerland;

Diplomata® from Koppert, Brazil; Vivus® Max from AgBiTech Pty Ltd., Queensland,

Australia), Helicoverpa zea single capsid nucleopolyhedrovirus (HzSNPV) (e. g. Gemstar® from Certis LLC, USA), Helicoverpa zea nucleopolyhedrovirus ABA-NPV-U (e. g. Heligen® from AgBiTech Pty Ltd., Queensland, Australia), Heterorhabditis bacteriophora (e. g.

Nemasys® G from BASF Agricultural Specialities Limited, UK), Isaria fumosorosea Apopka-97 isolated from mealy bug on gynura in Apopka, Florida, U.S.A. (ATCC 20874; Biocontrol Science Technol. 22(7), 747-761 , 2012; e. g. PFR-97™ or PreFeRal® from Certis LLC,

USA), Metarhizium anisopliae var. anisopliae F52 also called 275 or V275 isolated from codling moth in Austria (DSM 3884, ATCC 90448; e. g. Met52® Novozymes Biologicals BioAg Group, Canada), Metschnikowia fructicola 277 isolated from grapes in the central part of Israel (US 6,994,849; NRRL Y-30752; e. g. formerly Shemer® from Agrogreen, Israel), Paecilomyces ilacinus 251 isolated from infected nematode eggs in the Philippines (AGAL 89/030550; W01991/02051 ; Crop Protection 27, 352-361 , 2008; e. g. BioAct®from Bayer CropScience AG, Germany and MeloCon® from Certis, USA), Pasteuria nishizawae Pn1 isolated from a soybean field in the mid-2000s in Illinois, U.S.A. (ATCC SD-5833; Federal Register 76(22), 5808, February 2, 201 1 ; e.g. Clariva™ PN from Syngenta Crop Protection, LLC, USA), Penicillium bilaiae (also called P. bilaii ) strains ATCC 18309 (= ATCC 74319), ATCC 20851 and/or ATCC 22348 (= ATCC 74318) originally isolated from soil in Alberta, Canada (Fertilizer Res. 39, 97-103, 1994; Can. J. Plant Sci. 78(1 ), 91-102, 1998;

US 5,026,417, WO 1995/017806; e. g. Jump Start®, Provide® from Novozymes Biologicals BioAg Group, Canada), Reynoutria sachalinensis extract (EP 0307510 B1 ; e. g. Regalia®

SC from Marrone Bioinnovations, Davis, CA, USA or Milsana® from BioFa AG, Germany), Steinernema carpocapsae (e. g. Millenium® from BASF Agricultural Specialities Limited,

UK), S. feltiae (e. g. Nemashield® from BioWorks, Inc., USA; Nemasys® from BASF

Agricultural Specialities Limited, UK), Streptomyces microflavus NRRL B-50550

(WO 2014/124369; Bayer CropScience, Germany), T. harzianum T-22 also called KRL-AG2 (ATCC 20847; BioControl 57, 687-696, 2012; e. g. Plantshield® from BioWorks Inc., USA or SabrEx™ from Advanced Biological Marketing Inc., Van Wert, OH, USA).

According to the invention, the solid material (dry matter) of the biopesticides (with the exception of oils such as Neem oil) are considered as active components (e.g. to be obtained after drying or evaporation of the extraction or suspension medium in case of liquid formulations of the microbial pesticides).

In accordance with the present invention, the weight ratios and percentages used herein for a biological extract such as Quillay extract are based on the total weight of the dry content (solid material) of the respective extract(s).

The total weight ratios of compositions comprising at least one microbial pesticide in the form of viable microbial cells including dormant forms, can be determined using the amount of CFU of the respective microorganism to calculate the total weight of the respective active component with the following equation that 1 x 1010 CFU equals one gram of total weight of the respective active component. Colony forming unit is measure of viable microbial cells, in particular fungal and bacterial cells. In addition, here“CFU” may also be understood as the number of (juvenile) individual nematodes in case of (entomopathogenic) nematode biopesticides, such as Steinernema feltiae.

When mixtures comprising microbial pesticides are employed in crop protection, the application rates preferably range from about 1 x 106 to 5 x 1015 (or more) CFU/ha, preferably from about 1 x 108 to about 1 x 1013 CFU/ha, and even more preferably from about 1 x 109 to about 1 x 1012 CFU/ha. In the case of (entomopathogenic) nematodes as microbial pesticides (e. g. Steinernema feltiae), the application rates preferably range inform about 1 x 105 to 1 x 1012 (or more), more preferably from 1 x 108 to 1 x 1011 , even more preferably from 5 x 108 to 1 x 1010 individuals (e. g. in the form of eggs, juvenile or any other live stages, preferably in an infetive juvenile stage) per ha.

When mixtures comprising microbial pesticides are employed in seed treatment, the application rates with respect to plant propagation material preferably range from about 1 x 106 to 1 x 1012 (or more) CFU/seed. Preferably, the concentration is about 1 x 106 to about 1 x 109 CFU/seed. In the case of the microbial pesticides II, the application rates with respect to plant propagation material also preferably range from about 1 x 107 to 1 x 1014 (or more) CFU per 100 kg of seed, preferably from 1 x 109 to about 1 x 1012 CFU per 100 kg of seed.

The invention also relates to agrochemical compositions comprising an auxiliary and at least one compound of the present invention or a mixture thereof.

An agrochemical composition comprises a pesticidally effective amount of a compound of the present invention or a mixture thereof. The term "pesticidally effective amount" is defined below.

The compounds of the present invention or the mixtures thereof can be converted into customary types of agro-chemical compositions, e. g. solutions, emulsions, suspensions, dusts, powders, pastes, granules, pressings, capsules, and mixtures thereof. Examples for composition types are suspensions (e.g. SC, OD, FS), emulsifiable concentrates (e.g. EC), emulsions (e.g. EW, EO, ES, ME), capsules (e.g. CS, ZC), pastes, pastilles, wettable powders or dusts (e.g. WP, SP, WS, DP, DS), pressings (e.g. BR, TB, DT), granules (e.g. WG, SG, GR, FG, GG, MG), insecticidal articles (e.g. LN), as well as gel formulations for the treatment of plant propagation materials such as seeds (e.g. GF). These and further compositions types are defined in the“Catalogue of pesticide formulation types and international coding system”, Technical Mono-graph No. 2, 6th Ed. May 2008, CropLife International.

The compositions are prepared in a known manner, such as described by Mollet and Grube-mann, Formulation technology, Wiley VCH, Weinheim, 2001 ; or Knowles, New developments in crop protection product formulation, Agrow Reports DS243, T&F Informa, London, 2005.

Examples for suitable auxiliaries are solvents, liquid carriers, solid carriers or fillers, surfac tants, dispersants, emulsifiers, wetters, adjuvants, solubilizers, penetration enhancers, protec-tive colloids, adhesion agents, thickeners, humectants, repellents, attractants, feeding stimu-lants, compatibilizers, bactericides, anti-freezing agents, anti-foaming agents, colorants, tackifi-ers and binders.

Suitable solvents and liquid carriers are water and organic solvents, such as mineral oil frac-tions of medium to high boiling point, e.g. kerosene, diesel oil; oils of vegetable or animal origin; aliphatic, cyclic and aromatic hydrocarbons, e. g. toluene, paraffin,

tetrahydronaphthalene, al-kylated naphthalenes; alcohols, e.g. ethanol, propanol, butanol, benzylalcohol, cyclo^hexanol; glycols; DMSO; ketones, e.g. cyclohexanone; esters, e.g. lactates, carbonates, fatty acid esters, gamma-butyrolactone; fatty acids; phosphonates; amines; amides, e.g. N-methylpyrrolidone, fatty acid dimethylamides; and mixtures thereof.

Suitable solid carriers or fillers are mineral earths, e.g. silicates, silica gels, talc, kaolins, limestone, lime, chalk, clays, dolomite, diatomaceous earth, bentonite, calcium sulfate, magnesium sulfate, magnesium oxide; polysaccharide powders, e.g. cellulose, starch;

fertilizers, e.g. ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas; products of vegetable origin, e.g. cereal meal, tree bark meal, wood meal, nutshell meal, and mixtures thereof.

Suitable surfactants are surface-active compounds, such as anionic, cationic, nonionic and amphoteric surfactants, block polymers, polyelectrolytes, and mixtures thereof. Such surfactants can be used as emusifier, dispersant, solubilizer, wetter, penetration enhancer, protective colloid, or adjuvant. Examples of surfactants are listed in McCutcheon’s, Vol.1 : Emulsifiers & Detergents, McCutcheon’s Directories, Glen Rock, USA, 2008 (International Ed. or North American Ed.).

Suitable anionic surfactants are alkali, alkaline earth or ammonium salts of sulfonates, sul fates, phosphates, carboxylates, and mixtures thereof. Examples of sulfonates are alkylaryl-sulfonates, diphenylsulfonates, alpha-olefin sulfonates, lignine sulfonates, sulfonates of fatty acids and oils, sulfonates of ethoxylated alkylphenols, sulfonates of alkoxylated arylphenols, sulfonates of condensed naphthalenes, sulfonates of dodecyl- and tridecylbenzenes, sulfonates of naphthalenes and alkyhnaphthalenes, sulfosuccinates or sulfosuccinamates. Examples of sulfates are sulfates of fatty acids and oils, of ethoxylated alkylphenols, of alcohols, of ethox-ylated alcohols, or of fatty acid esters. Examples of phosphates are phosphate esters. Exam-pies of carboxylates are alkyl carboxylates, and carboxylated alcohol or alkylphenol eth-oxylates.

Suitable nonionic surfactants are alkoxylates, N-subsituted fatty acid amides, amine oxides, esters, sugar-based surfactants, polymeric surfactants, and mixtures thereof. Examples of alkoxylates are compounds such as alcohols, alkylphenols, amines, amides, arylphenols, fatty acids or fatty acid esters which have been alkoxylated with 1 to 50 equivalents. Ethylene oxide and/or propylene oxide may be employed for the alkoxylation, preferably ethylene oxide. Exam-pies of N-subsititued fatty acid amides are fatty acid glucamides or fatty acid alkanolamides. Examples of esters are fatty acid esters, glycerol esters or monoglycerides. Examples of sugar-based surfactants are sorbitans, ethoxylated sorbitans, sucrose and glucose esters or alkylpolyglucosides. Examples of polymeric surfactants are homo- or copolymers of vinylpyrrolidone, vinylalcohols, or vinylacetate.

Suitable cationic surfactants are quaternary surfactants, for example quaternary ammonium compounds with one or two hydrophobic groups, or salts of long-chain primary amines.

Suitable amphoteric surfactants are alkylbetains and imidazolines. Suitable block polymers are block polymers of the A-B or A-B-A type comprising blocks of polyethylene oxide and polypropylene oxide, or of the A-B-C type comprising alkanol, polyethylene oxide and polypropylene oxide. Suitable polyelectrolytes are polyacids or polybases. Examples of polyacids are alkali salts of polyacrylic acid or polyacid comb polymers. Examples of polybases are polyvinylamines or polyethyleneamines.

Suitable adjuvants are compounds, which have a neglectable or even no pesticidal activity themselves, and which improve the biological performance of the compounds of the present invention on the target. Examples are surfactants, mineral or vegetable oils, and other

auxilaries. Further examples are listed by Knowles, Adjuvants and additives, Agrow Reports DS256, T&F Informa UK, 2006, chapter 5.

Suitable thickeners are polysaccharides (e.g. xanthan gum, carboxymethylcellulose), anorganic clays (organically modified or unmodified), polycarboxylates, and silicates.

Suitable bactericides are bronopol and isothiazolinone derivatives such as alkylisothiazoli-nones and benzisothiazolinones.

Suitable anti-freezing agents are ethylene glycol, propylene glycol, urea and glycerin.

Suitable anti-foaming agents are silicones, long chain alcohols, and salts of fatty acids.

Suitable colorants (e.g. in red, blue, or green) are pigments of low water solubility and water-soluble dyes. Examples are inorganic colorants (e.g. iron oxide, titan oxide, iron hexacyanofer-rate) and organic colorants (e.g. alizarin-, azo- and phthalocyanine colorants).

Suitable tackifiers or binders are polyvinylpyrrolidons, polyvinylacetates, polyvinyl alcohols, polyacrylates, biological or synthetic waxes, and cellulose ethers.

Examples for composition types and their preparation are:

i) Water-soluble concentrates (SL, LS)

10-60 wt% of a compound I according to the invention and 5-15 wt% wetting agent (e.g. alcohol alkoxylates) are dissolved in water and/or in a water-soluble solvent (e.g. alcohols) up to 100 wt%. The active substance dissolves upon dilution with water.

ii) Dispersible concentrates (DC)

5-25 wt% of a compound I according to the invention and 1-10 wt% dispersant (e. g. polyvi nylpyrrolidone) are dissolved in up to 100 wt% organic solvent (e.g. cyclohexanone). Dilution with water gives a dispersion.

iii) Emulsifiable concentrates (EC)

15-70 wt% of a compound I according to the invention and 5-10 wt% emulsifiers (e.g. calcium dodecylbenzenesulfonate and castor oil ethoxylate) are dissolved in up to 100 wt% water-insoluble organic solvent (e.g. aromatic hydrocarbon). Dilution with water gives an emulsion.

iv) Emulsions (EW, EO, ES)

5-40 wt% of a compound I according to the invention and 1-10 wt% emulsifiers (e.g.

calcium dodecylbenzenesulfonate and castor oil ethoxylate) are dissolved in 20-40 wt% water-insoluble organic solvent (e.g. aromatic hydrocarbon). This mixture is introduced into up to 100 wt% water by means of an emulsifying machine and made into a homogeneous emulsion. Dilution with water gives an emulsion.

v) Suspensions (SC, OD, FS)

In an agitated ball mill, 20-60 wt% of a compound I according to the invention are comminuted with addition of 2-10 wt% dispersants and wetting agents (e.g. sodium lignosulfonate and alcohol ethoxylate), 0,1-2 wt% thickener (e.g. xanthan gum) and up to 100 wt% water to give a fine active substance suspension. Dilution with water gives a stable suspension of the active sub-stance. For FS type composition up to 40 wt% binder (e.g. polyvinylalcohol) is added.

vi) Water-dispersible granules and water-soluble granules (WG, SG)

50-80 wt% of a compound I according to the invention are ground finely with addition of up to 100 wt% dispersants and wetting agents (e.g. sodium lignosulfonate and alcohol ethoxylate) and prepared as water-dispersible or water-soluble granules by means of technical appliances (e. g. extrusion, spray tower, fluidized bed). Dilution with water gives a stable dispersion or solution of the active substance.

vii) Water-dispersible powders and water-soluble powders (WP, SP, WS)

50-80 wt% of a compound I according to the invention are ground in a rotor-stator mill with ad-dition of 1-5 wt% dispersants (e.g. sodium lignosulfonate), 1-3 wt% wetting agents (e.g. alcohol ethoxylate) and up to 100 wt% solid carrier, e.g. silica gel. Dilution with water gives a stable dis-persion or solution of the active substance.

viii) Gel (GW, GF)

In an agitated ball mill, 5-25 wt% of a compound I according to the invention are comminuted with addition of 3-10 wt% dispersants (e.g. sodium lignosulfonate), 1-5 wt% thickener (e.g. car-boxymethylcellulose) and up to 100 wt% water to give a fine suspension of the active sub-stance. Dilution with water gives a stable suspension of the active substance.

ix) Microemulsion (ME)

5-20 wt% of a compound I according to the invention are added to 5-30 wt% organic solvent blend (e.g. fatty acid dimethylamide and cyclohexanone), 10-25 wt% surfactant blend (e.g. alkohol ethoxylate and arylphenol ethoxylate), and water up to 100 %. This mixture is stirred for 1 h to produce spontaneously a thermodynamically stable microemulsion.

x) Microcapsules (CS)

An oil phase comprising 5-50 wt% of a compound I according to the invention, 0-40 wt% water insoluble organic solvent (e.g. aromatic hydrocarbon), 2-15 wt% acrylic monomers (e.g. methylmethacrylate, methacrylic acid and a di- or triacrylate) are dispersed into an aqueous solution of a protective colloid (e.g. polyvinyl alcohol). Radical polymerization initiated by a radi-cal initiator results in the formation of poly(meth)acrylate microcapsules. Alternatively, an oil phase comprising 5-50 wt% of a compound I according to the invention, 0-40 wt% water insolu-ble organic solvent (e.g. aromatic hydrocarbon), and an isocyanate monomer (e.g. diphenylme-thene-4,4’-diisocyanatae) are dispersed into an aqueous solution of a protective colloid (e.g. polyvinyl alcohol). The addition of a polyamine (e.g.

hexamethylenediamine) results in the for-mation of a polyurea microcapsule. The monomers amount to 1-10 wt%. The wt% relate to the total CS composition.

xi) Dustable powders (DP, DS)

1-10 wt% of a compound I according to the invention are ground finely and mixed intimately with up to 100 wt% solid carrier, e.g. finely divided kaolin.

xii) Granules (GR, FG)

0.5-30 wt% of a compound I according to the invention is ground finely and associated with up to 100 wt% solid carrier (e.g. silicate). Granulation is achieved by extrusion, spray-drying or the fluidized bed.

xiii) Ultra-low volume liquids (UL)

1-50 wt% of a compound I according to the invention are dissolved in up to 100 wt% organic solvent, e.g. aromatic hydrocarbon.

The compositions types i) to xi) may optionally comprise further auxiliaries, such as 0.1-1 wt% bactericides, 5-15 wt% anti-freezing agents, 0.1-1 wt% anti-foaming agents, and 0.1-1 wt% col-orants.

The agrochemical compositions generally comprise between 0.01 and 95%, preferably be tween 0.1 and 90%, and most preferably between 0.5 and 75%, by weight of active sub stance. The active substances are employed in a purity of from 90% to 100%, preferably from 95% to 100% (according to NMR spectrum).

Various types of oils, wetters, adjuvants, fertilizer, or micronutrients, and other pesticides (e.g. herbicides, insecticides, fungicides, growth regulators, safeners) may be added to the active substances or the compositions cormprising them as premix or, if appropriate not until immediately prior to use (tank mix). These agents can be admixed with the compositions according to the invention in a weight ratio of 1 :100 to 100:1 , preferably 1 :10 to 10:1.

The user applies the composition according to the invention usually from a predosage de vice, a knapsack sprayer, a spray tank, a spray plane, or an irrigation system. Usually, the agrochemical composition is made up with water, buffer, and/or further auxiliaries to the desired application concentration and the ready-to-use spray liquor or the agrochemical composition according to the invention is thus obtained. Usually, 20 to 2000 liters, preferably 50 to 400 liters, of the ready-to-use spray liquor are applied per hectare of agricultural useful area.

According to one embodiment, individual components of the composition according to the in-vention such as parts of a kit or parts of a binary or ternary mixture may be mixed by the user himself in a spray tank and further auxiliaries may be added, if appropriate.

In a further embodiment, either individual components of the composition according to the invention or partially premixed components, e. g. components comprising compounds of the present invention and/or mixing partners as defined above, may be mixed by the user in a spray tank and further auxiliaries and additives may be added, if appropriate.

In a further embodiment, either individual components of the composition according to the in-vention or partially premixed components, e. g. components comprising compounds of the present invention and/or mixing partners as defined above, can be applied jointly (e.g. after tank mix) or consecutively.

The compounds of the present invention are suitable for use in protecting crops, plants, plant propagation materials, such as seeds, or soil or water, in which the plants are growing, from attack or infestation by animal pests. Therefore, the present invention also relates to a plant protection method, which comprises contacting crops, plants, plant propagation materials, such as seeds, or soil or water, in which the plants are growing, to be protected from attack or infestation by animal pests, with a pesticidally effective amount of a compound of the present invention.

The compounds of the present invention are also suitable for use in combating or controlling animal pests. Therefore, the present invention also relates to a method of combating or controlling animal pests, which comprises contacting the animal pests, their habitat, breeding ground, or food supply, or the crops, plants, plant propagation materials, such as seeds, or soil, or the area, material or environment in which the animal pests are growing or may grow, with a pesticidally effective amount of a compound of the present invention.

The compounds of the present invention are effective through both contact and ingestion. Furthermore, the compounds of the present invention can be applied to any and all developmental stages, such as egg, larva, pupa, and adult.

The compounds of the present invention can be applied as such or in form of compositions comprising them as defined above. Furthermore, the compounds of the present invention can be applied together with a mixing partner as defined above or in form of compositions comprising said mixtures as defined above. The components of said mixture can be applied simultaneously, jointly or separately, or in succession, that is immediately one after another and thereby creating the mixture“in situ” on the desired location, e.g. the plant, the sequence, in the case of separate application, generally not having any effect on the result of the control measures.

The application can be carried out both before and after the infestation of the crops, plants, plant propagation materials, such as seeds, soil, or the area, material or environment by the pests.

Suitable application methods include inter alia soil treatment, seed treatment, in furrow application, and foliar application. Soil treatment methods include drenching the soil, drip irrigation (drip application onto the soil), dipping roots, tubers or bulbs, or soil injection. Seed treatment techniques include seed dressing, seed coating, seed dusting, seed soaking, and seed pelleting. In furrow applications typically include the steps of making a furrow in

cultivated land, seeding the furrow with seeds, applying the pesticidally active compound to the furrow, and closing the furrow. Foliar application refers to the application of the pesticidally active compound to plant foliage, e.g. through spray equipment. For foliar applications, it can be advantageous to modify the behavior of the pests by use of pheromones in combination with the compounds of the present invention. Suitable pheromones for specific crops and pests are known to a skilled person and publicly available from databases of pheromones and semiochemicals, such as http://www.pherobase.com.

As used herein, the term "contacting" includes both direct contact (applying the

compounds/compositions directly on the animal pest or plant - typically to the foliage, stem or roots of the plant) and indirect contact (applying the compounds/compositions to the locus, i.e. habitat, breeding ground, plant, seed, soil, area, material or environment in which a pest is growing or may grow, of the animal pest or plant).

The term“animal pest” includes arthropods, gastropods, and nematodes. Preferred animal pests according to the invention are arthropods, preferably insects and arachnids, in particular insects. Insects, which are of particular relevance for crops, are typically referred to as crop insect pests.

The term "crop" refers to both, growing and harvested crops.

The term“plant” includes cereals, e.g. durum and other wheat, rye, barley, triticale, oats, rice, or maize (fodder maize and sugar maize / sweet and field corn); beet, e.g. sugar beet or fodder beet; fruits, such as pomes, stone fruits or soft fruits, e.g. apples, pears, plums, peaches, nectarines, almonds, cherries, papayas, strawberries, raspberries, blackberries or gooseberries; leguminous plants, such as beans, lentils, peas, alfalfa or soybeans; oil plants, such as rapeseed (oilseed rape), turnip rape, mustard, olives, sunflowers, coconut, cocoa beans, castor oil plants, oil palms, ground nuts or soybeans; cucurbits, such as squashes, pumpkins, cucumber or melons; fiber plants, such as cotton, flax, hemp or jute; citrus fruit, such as oranges, lemons, grapefruits or mandarins; vegetables, such as eggplant, spinach, lettuce (e.g. iceberg lettuce), chicory, cabbage, asparagus, cabbages, carrots, onions, garlic, leeks, tomatoes, potatoes, cucurbits or sweet peppers; lauraceous plants, such as avocados, cinnamon or camphor; energy and raw material plants, such as corn, soybean, rapeseed, sugar cane or oil palm; tobacco; nuts, e.g. walnuts; pistachios; coffee; tea; bananas; vines (table grapes and grape juice grape vines); hop; sweet leaf (also called Stevia); natural rubber plants or ornamental and forestry plants, such as flowers (e.g. carnation, petunias, geranium/pelargoniums, pansies and impatiens), shrubs, broad-leaved trees (e.g. poplar) or evergreens, e.g. conifers; eucalyptus; turf; lawn; grass such as grass for animal feed or ornamental uses. Preferred plants include potatoes sugar beets, tobacco, wheat, rye, barley, oats, rice, corn, cotton, soybeans, rapeseed, legumes, sunflowers, coffee or sugar cane; fruits; vines; ornamentals; or vegetables, such as cucumbers, tomatoes, beans or squashes.

The term“plant” is to be understood as including wild type plants and plants, which have been modified by either conventional breeding, or mutagenesis or genetic engineering, or by a combination thereof.

Plants, which have been modified by mutagenesis or genetic engineering, and are of particular commercial importance, include alfalfa, rapeseed (e.g. oilseed rape), bean, carnation, chicory, cotton, eggplant, eucalyptus, flax, lentil, maize, melon, papaya, petunia, plum, poplar, potato, rice, soybean, squash, sugar beet, sugarcane, sunflower, sweet pepper, tobacco, tomato, and cereals (e.g. wheat), in particular maize, soybean, cotton, wheat, and rice. In plants, which have been modified by mutagenesis or genetic engineering, one or more genes have been mutagenized or integrated into the genetic material of the plant. The one or more mutagenized or integrated genes are preferably selected from pat, epsps, crylAb, bar, cry1 Fa2, crylAc, cry34Ab1 , cry35AB1 , cry3A, cryF, cry1 F, mcry3a, cry2Ab2, cry3Bb1 , cry1A.105, dfr, barnase, vip3Aa20, barstar, als, bxn, bp40, asn1 , and ppo5. The mutagenesis or integration of the one or more genes is performed in order to improve certain properties of the plant. Such properties, also known as traits, include abiotic stress tolerance, altered growth/yield, disease resistance, herbicide tolerance, insect resistance, modified product quality, and pollination control. Of these properties, herbicide tolerance, e.g. imidazolinone tolerance, glyphosate tolerance, or glufosinate tolerance, is of particular importance. Several plants have been rendered tolerant to herbicides by mutagenesis, for example Clearfield® oilseed rape being tolerant to imidazolinones, e.g. imazamox. Alternatively, genetic engineering methods have been used to render plants, such as soybean, cotton, corn, beets and oil seed rape, tolerant to herbicides, such as glyphosate and glufosinate, some of which are commercially available under the trade names RoundupReady® (glyphosate) and LibertyLink® (glufosinate). Furthermore, insect resistance is of importance, in particular lepidopteran insect resistance and coleopteran insect resistance. Insect resistance is typically achieved by modifying plants by integrating cry and/or vip genes, which were isolated from Bacillus thuringiensis (Bt), and code for the respective Bt toxins. Genetically modified plants with insect resistance are commercially available under trade names including WideStrike®, Bollgard®, Agrisure®, Herculex®, YieldGard®, Genuity®, and Intacta®. Plants may be modified by mutagenesis or genetic engineering either in terms of one property (singular traits) or in terms of a combination of properties (stacked traits). Stacked traits, e.g. the combination of herbicide tolerance and insect resistance, are of increasing importance. In general, all relevant modified plants in connection with singular or stacked traits as well as detailed information as to the

mutagenized or integrated genes and the respective events are available from websites of the organizations“International Service for the Acquisition of Agri-biotech Applications

(ISAAA)” (http://www.isaaa.org/gmapprovaldatabase) and“Center for Environmental Risk Assessment (CERA)” (http://cera-qmc.org/GMCropDatabase)·

It has surprisingly been found that the pesticidal activity of the compounds of the present invention may be enhanced by the insecticidal trait of a modified plant. Furthermore, it has been found that the compounds of the present invention are suitable for preventing insects to become resistant to the insecticidal trait or for combating pests, which already have become resistant to the insecticidal trait of a modified plant. Moreover, the compounds of the present invention are suitable for combating pests, against which the insecticidal trait is not effective, so that a complementary insecticidal activity can advantageously be used.

The term "plant propagation material" refers to all the generative parts of the plant such as seeds and vegetative plant material such as cuttings and tubers (e.g. potatoes), which can be used for the multiplication of the plant. This includes seeds, roots, fruits, tubers, bulbs, rhizomes, shoots, sprouts and other parts of plants. Seedlings and young plants, which are to be transplanted after germination or after emergence from soil, may also be included. These plant propagation materials may be treated prophylactically with a plant protection compound either at or before planting or transplanting.

The term“seed” embraces seeds and plant propagules of all kinds including but not limited to true seeds, seed pieces, suckers, corms, bulbs, fruit, tubers, grains, cuttings, cut shoots and the like, and means in a preferred embodiment true seeds.

In general, "pesticidally effective amount" means the amount of active ingredient needed to achieve an observable effect on growth, including the effects of necrosis, death, retardation, prevention, and removal, destruction, or otherwise diminishing the occurrence and activity of the target organism. The pesticidally effective amount can vary for the various

compounds/compositions used in the invention. A pesticidally effective amount of the compositions will also vary according to the prevailing conditions such as desired pesticidal effect and duration, weather, target species, locus, mode of application, and the like.

In the case of soil treatment, in furrow application or of application to the pests dwelling place or nest, the quantity of active ingredient ranges from 0.0001 to 500 g per 100 m2, preferably from 0.001 to 20 g per 100 m2.

For use in treating crop plants, e.g. by foliar application, the rate of application of the active ingredients of this invention may be in the range of 0.0001 g to 4000 g per hectare, e.g. from 1 g to 2 kg per hectare or from 1 g to 750 g per hectare, desirably from 1 g to 100 g per hectare, more desirably from 10 g to 50 g per hectare, e.g., 10 to 20 g per hectare, 20 to 30 g per hectare, 30 to 40 g per hectare, or 40 to 50 g per hectare.

The compounds of the present invention are particularly suitable for use in the treatment of seeds in order to protect the seeds from insect pests, in particular from soil-living insect pests, and the resulting seedling’s roots and shoots against soil pests and foliar insects. The present invention therefore also relates to a method for the protection of seeds from insects, in particular from soil insects, and of the seedling's roots and shoots from insects, in particular from soil and foliar insects, said method comprising treating the seeds before sowing and/or after pregermination with a compound of the present invention. The protection of the seedling's roots and shoots is preferred. More preferred is the protection of seedling’s shoots from piercing and sucking insects, chewing insects and nematodes.

The term“seed treatment” comprises all suitable seed treatment techniques known in the art, such as seed dressing, seed coating, seed dusting, seed soaking, seed pelleting, and in furrow application methods. Preferably, the seed treatment application of the active compound is carried out by spraying or by dusting the seeds before sowing of the plants and before emergence of the plants.

The present invention also comprises seeds coated with or containing the active compound. The term "coated with and/or containing" generally signifies that the active ingredient is for the most part on the surface of the propagation product at the time of application, although a greater or lesser part of the ingredient may penetrate into the propagation product, depending on the method of application. When the said propagation product is (re)planted, it may absorb the active ingredient.

Suitable seed is for example seed of cereals, root crops, oil crops, vegetables, spices, ornamentals, for example seed of durum and other wheat, barley, oats, rye, maize (fodder maize and sugar maize / sweet and field corn), soybeans, oil crops, crucifers, cotton, sunflowers, bananas, rice, oilseed rape, turnip rape, sugarbeet, fodder beet, eggplants, potatoes, grass, lawn, turf, fodder grass, tomatoes, leeks, pumpkin/squash, cabbage, iceberg lettuce, pepper, cucumbers, melons, Brassica species, melons, beans, peas, garlic, onions, carrots, tuberous plants such as potatoes, sugar cane, tobacco, grapes, petunias, geranium/pelargoniums, pansies and impatiens.

In addition, the active compound may also be used for the treatment of seeds from plants, which have been modified by mutagenisis or genetic engineering, and which e.g. tolerate the action of herbicides or fungicides or insecticides. Such modified plants have been described in detail above.

Conventional seed treatment formulations include for example flowable concentrates FS, solutions LS, suspoemulsions (SE), powders for dry treatment DS, water dispersible powders for slurry treatment WS, water-soluble powders SS and emulsion ES and EC and gel formulation GF. These formulations can be applied to the seed diluted or undiluted.

Application to the seeds is carried out before sowing, either directly on the seeds or after having pregerminated the latter. Preferably, the formulations are applied such that germination is not included.

The active substance concentrations in ready-to-use formulations, which may be obtained after two-to-tenfold dilution, are preferably from 0.01 to 60% by weight, more preferably from 0.1 to 40 % by weight.

In a preferred embodiment a FS formulation is used for seed treatment. Typically, a FS formulation may comprise 1-800 g/l of active ingredient, 1-200 g/l Surfactant, 0 to 200 g/l antifreezing agent, 0 to 400 g/l of binder, 0 to 200 g/l of a pigment and up to 1 liter of a solvent, preferably water.

Especially preferred FS formulations of the compounds of the present invention for seed treatment usually comprise from 0.1 to 80% by weight (1 to 800 g/l) of the active ingredient, from 0.1 to 20 % by weight (1 to 200 g/l) of at least one surfactant, e.g. 0.05 to 5 % by weight of a wetter and from 0.5 to 15 % by weight of a dispersing agent, up to 20 % by weight, e.g. from 5 to 20 % of an anti-freeze agent, from 0 to 15 % by weight, e.g. 1 to 15 % by weight of a pigment and/or a dye, from 0 to 40 % by weight, e.g. 1 to 40 % by weight of a binder (sticker /adhesion agent), optionally up to 5 % by weight, e.g. from 0.1 to 5 % by weight of a thickener, optionally from 0.1 to 2 % of an anti-foam agent, and optionally a preservative such as a biocide, antioxidant or the like, e.g. in an amount from 0.01 to 1 % by weight and a filler/vehicle up to 100 % by weight.

In the treatment of seed, the application rates of the compounds of the invention are generally from 0.1 g to 10 kg per 100 kg of seed, preferably from 1 g to 5 kg per 100 kg of seed, more preferably from 1 g to 1000 g per 100 kg of seed and in particular from 1 g to 200 g per 100 kg of seed, e.g. from 1 g to 100 g or from 5 g to 100 g per 100 kg of seed.

The invention therefore also relates to seed comprising a compound of the present invention, or an agriculturally useful salt thereof, as defined herein. The amount of the compound of the present invention or the agriculturally useful salt thereof will in general vary from 0.1 g to 10 kg per 100 kg of seed, preferably from 1 g to 5 kg per 100 kg of seed, in particular from 1 g to 1000 g per 100 kg of seed. For specific crops such as lettuce the rate can be higher.

The invention also relates to composition comprising seed and a compound of the present invention, or an agriculturally useful salt thereof, as defined herein. The amount of the compound of the present invention or the agriculturally useful salt thereof will in general vary from 0.1 g to 10 kg per 100 kg of seed, preferably from 1 g to 5 kg per 100 kg of seed, in particular from 1 g to 1000 g per 100 kg of seed. For specific crops such as lettuce the rate can be higher.

The compounds of the present invention may also be used for improving the health of a plant. Therefore, the present invention also relates to a method for improving plant health by treating a plant, plant propagation material and/or the locus where the plant is growing or is to grow with an effective and non-phytotoxic amount of a compound of the present invention.

As used herein“an effective and non-phytotoxic amount” means that the compound is used in a quantity which allows to obtain the desired effect but which does not give rise to any phytotoxic symptom on the treated plant or on the plant grown from the treated propagule or treated soil.

The terms“plant” and“plant propagation material” are defined above.

"Plant health" is defined as a condition of the plant and/or its products which is determined by several aspects alone or in combination with each other such as yield (for example increased biomass and/or increased content of valuable ingredients), quality (for example improved content or composition of certain ingredients or shelf life), plant vigour (for example improved plant growth and/or greener leaves (“greening effect”), tolerance to abiotic (for example drought) and/or biotic stress (for example disease) and production efficiency (for example, harvesting efficiency, processability).

The above identified indicators for the health condition of a plant may be interdependent and may result from each other. Each indicator is defined in the art and can be determined by methods known to a skilled person.

The compounds of the invention are also suitable for use against non-crop insect pests. For use against said non-crop pests, compounds of the present invention can be used as bait composition, gel, general insect spray, aerosol, as ultra-low volume application and bed net (impregnated or surface applied). Furthermore, drenching and rodding methods can be used.

As used herein, the term“non-crop insect pest” refers to pests, which are particularly relevant for non-crop targets, such as ants, termites, wasps, flies, ticks, mosquitos, crickets, or cockroaches.

The bait can be a liquid, a solid or a semisolid preparation (e.g. a gel). The bait employed in the composition is a product, which is sufficiently attractive to incite insects such as ants, termites, wasps, flies, mosquitos, crickets etc. or cockroaches to eat it. The attractiveness can be manipulated by using feeding stimulants or sex pheromones. Food stimulants are chosen, for example, but not exclusively, from animal and/or plant proteins (meat-, fish- or blood meal, insect parts, egg yolk), from fats and oils of animal and/or plant origin, or mono-, oligo- or polyorganosaccharides, especially from sucrose, lactose, fructose, dextrose, glucose, starch, pectin or even molasses or honey. Fresh or decaying parts of fruits, crops, plants, animals, insects or specific parts thereof can also serve as a feeding stimulant. Sex pheromones are known to be more insect specific. Specific pheromones are described in the literature (e.g. http://www.pherobase.com), and are known to those skilled in the art.

For use in bait compositions, the typical content of active ingredient is from 0.001 weight % to 15 weight %, desirably from 0.001 weight % to 5% weight % of active compound.

Formulations of the compounds of the present invention as aerosols (e.g in spray cans), oil sprays or pump sprays are highly suitable for the non-professional user for controlling pests such as flies, fleas, ticks, mosquitos or cockroaches. Aerosol recipes are preferably composed of the active compound, solvents, furthermore auxiliaries such as emulsifiers, perfume oils, if appropriate stabilizers, and, if required, propellants.

The oil spray formulations differ from the aerosol recipes in that no propellants are used.

For use in spray compositions, the content of active ingredient is from 0.001 to 80 weights %, preferably from 0.01 to 50 weight % and most preferably from 0.01 to 15 weight %.

The compounds of the present invention and its respective compositions can also be used in mosquito and fumigating coils, smoke cartridges, vaporizer plates or long-term vaporizers and also in moth papers, moth pads or other heat-independent vaporizer systems.

Methods to control infectious diseases transmitted by insects (e.g. malaria, dengue and yellow fever, lymphatic filariasis, and leishmaniasis) with compounds of the present invention and its respective compositions also comprise treating surfaces of huts and houses, air spraying and impregnation of curtains, tents, clothing items, bed nets, tsetse-fly trap or the like. Insecticidal compositions for application to fibers, fabric, knitgoods, nonwovens, netting material or foils and tarpaulins preferably comprise a mixture including the insecticide, optionally a repellent and at least one binder.

The compounds of the present invention and its compositions can be used for protecting wooden materials such as trees, board fences, sleepers, frames, artistic artifacts, etc. and buildings, but also construction materials, furniture, leathers, fibers, vinyl articles, electric wires and cables etc. from ants and/or termites, and for controlling ants and termites from doing harm to crops or human being (e.g. when the pests invade into houses and public facilities).

Customary application rates in the protection of materials are, for example, from 0.001 g to 2000 g or from 0.01 g to 1000 g of active compound per m2 treated material, desirably from 0.1 g to 50 g per m2.

Insecticidal compositions for use in the impregnation of materials typically contain from 0.001 to 95 weight %, preferably from 0.1 to 45 weight %, and more preferably from 1 to 25 weight % of at least one repellent and/or insecticide.

The compounds of the the present invention are especially suitable for efficiently combating animal pests such as arthropods, gastropods and nematodes including but not limited to: insects from the order of Lepidoptera, for example Achroia grisella, Acleris spp. such as A. fimbriana, A. gloverana, A. variana; Acrolepiopsis assectella, Acronicta major, Adoxophyes spp. such as A. cyrtosema, A. orana; Aedia leucomelas, Agrotis spp. such as A.

exclamationis, A. fucosa, A. ipsilon, A. orthogoma, A. segetum, A. subterranea; Alabama argillacea, Aleurodicus dispersus, Alsophila pometaria, Ampelophaga rubiginosa, Amyelois

transitella, Anacampsis sarcitella, Anagasta kuehniella, Anarsia lineatella, Anisota senatoria, Antheraea pernyi, Anticarsia (=Thermesia) spp. such as A. gemmatalis; Apamea spp., Aproaerema modicella, Archips spp. such as A. argyrospila, A. fuscocupreanus, A. rosana,

A. xyloseanus; Argyresthia conjugella, Argyroploce spp., Argyrotaenia spp. such as A.

velutinana; Athetis mindara, Austroasca viridigrisea, Autographa gamma, Autographa nigrisigna, Barathra brassicae, Bedellia spp., Bonagota salubricola, Borbo cinnara,

Bucculatrix thurberiella, Bupalus piniarius, Busseola spp., Cacoecia spp. such as C.

murinana, C. podana; Cactoblastis cactorum, Cadra cautella, Calingo braziliensis, Caloptilis theivora, Capua reticulana, Carposina spp. such as C. niponensis, C. sasakii; Cephus spp., Chaetocnema aridula, Cheimatobia brumata, Chilo spp. such as C. Indicus, C. suppressalis,

C. partellus; Choreutis pariana, Choristoneura spp. such as C. conflictana, C. fumiferana, C. longicellana, C. murinana, C. occidentalis, C. rosaceana; Chrysodeixis (=Pseudoplusia) spp. such as C. eriosoma, C. includens; Cirphis unipuncta, Clysia ambiguella, Cnaphalocerus spp., Cnaphalocrocis medinalis, Cnephasia spp., Cochylis hospes, Coleophora spp., Colias eurytheme, Conopomorpha spp., Conotrachelus spp., Copitarsia spp., Corcyra cephalonica, Crambus caliginosellus, Crambus teterrellus, Crocidosema (=Epinotia) aporema, Cydalima (=Diaphania) perspectalis, Cydia (=Carpocapsa) spp. such as C. pomonella, C. latiferreana; Dalaca noctuides, Datana integerrima, Dasychira pinicola, Dendrolimus spp. such as D. pini,

D. spectabilis, D. sibiricus; Desmia funeralis, Diaphania spp. such as D. nitidalis, D.

hyalinata; Diatraea grandiosella, Diatraea saccharalis, Diphthera festiva, Earias spp. such as

E. insulana, E. vittella; Ecdytolopha aurantianu, Egira (=Xylomyges) curialis, Elasmopalpus lignosellus, Eldana saccharina, Endopiza viteana, Ennomos subsignaria, Eoreuma loftini, Ephestia spp. such as £. cautella, E. elutella, E. kuehniella; Epinotia aporema, Epiphyas postvittana, Erannis tiliaria, Erionota thrax, Etiella spp., Eulia spp., Eupoecilia ambiguella, Euproctis chrysorrhoea, Euxoa spp., Evetria bouliana, Faronta albilinea, Feltia spp. such as

F. subterranean; Galleria mellonella, Gracillaria spp., Grapholita spp. such as G. funebrana,

G. molesta, G. inopinata; Halysidota spp., Harrisina americana, Hedylepta spp., Helicoverpa spp. such as H. armigera (=Heliothis armigera), H. zea (=Heliothis zea); Heliothis spp. such as H. assulta, H. subflexa, H. virescens; Hellula spp. such as H. undalis, H. rogatalis;

Helocoverpa gelotopoeon, Flemileuca oliviae, Herpetogramma licarsisalis, Hibernia defoliaria, Hofmannophila pseudospretella, Homoeosoma electellum, Homona magnanima, Hypena scabra, Hyphantria cunea, Hyponomeuta padella, Hyponomeuta malinellus, Kakivoria flavofasciata, Keiferia lycopersicella, Lam bd in a fiscellaria fiscellaria, Lambdina fiscellaria lugubrosa, Lamprosema indicata, Laspeyresia molesta, Leguminivora

glycinivorella, Lerodea eufala, Leucinodes orbonalis, Leucoma salicis, Leucoptera spp. such as L. coffeella, L. scitella; Leuminivora lycinivorella, Lithocolletis blancardella, Lithophane antennata, Llattia octo (=Amyna axis), Lobesia botrana, Lophocampa spp., Loxagrotis

albicosta, Loxostege spp. such as L. sticticalis, L cereralis; Lymantria spp. such as L. dispar,

L. monacha; Lyonetia clerkella, Lyonetia prunifoliella, Malacosoma spp. such as M.

americanum, M. californicum, M. constrictum, M. neustria; Mamestra spp. such as M.

brassicae, M. configurata; Mamstra brassicae, Manduca spp. such as M. quinquemaculata,

M. sexta; Marasmia spp, Marmara spp., Maruca testulalis, Megalopyge lanata, Melanchra picta, Melanitis leda, Mods spp. such as M. lapites, M. repanda; Mods latipes, Monochroa fragariae, Mythimna separata, Nemapogon doacella, Neoleudnodes elegantalis, Nepytia spp., Nymphula spp., Oiketicus spp., Omiodes indicata, Omphisa anastomosalis,

Operophtera brumata, Orgyia pseudotsugata, Oria spp., Orthaga thyrisalis, Ostrinia spp. such as O. nubilalis; Oulema oryzae, Paleacrita vernata, Panolis flammea, Parnara spp., Papaipema nebris, Papilio cresphontes, Paramyelois transitella, Paranthrene regalis, Paysandisia archon, Pedinophora spp. such as P. gossypiella; Peridroma sauda,

Peri leu coptera spp., such as P. coffeella; Phalera bucephala, Phryganidia californica, Phthorimaea spp. such as P. operculella; Phyllocnistis dtrella, Phyllonoryder spp. such as P. blancardella, P. crataegella, P. issikii, P. ringoniella; Pieris spp. such as P. brassicae, P. rapae, P. napi; Pilocrocis tripunctata, Plathypena scabra, Platynota spp. such as P.

flavedana, P. idaeusalis, P. stultana; Platyptilia carduidactyla, Plebejus argus, Plodia interpunctella, Plusia spp, Plutella maculipennis, Plutella xylostella, Pontia protodica, Prays spp., Prodenia spp., Proxenus lepigone, Pseudaletia spp. such as P. sequax, P. unipuncta; Pyrausta nubilalis, Rachiplusia nu, Richia albicosta, Rhizobius ventralis, Rhyacionia frustrana, Sabulodes aegrotata, Schizura concinna, Schoenobius spp., Schreckensteinia festaliella, Scirpophaga spp. such as S. incertulas, S. innotata; Scotia segetum, Sesamia spp. such as S. inferens, Seudyra subflava, Sitotroga cerealella, Sparganothis pilleriana, Spilonota lechriaspis, S. ocellana, Spodoptera (=Lamphygma) spp. such as S. cosmoides, S. eridania, S. exigua, S. frugiperda, S. latisfascia, S. littoralis, S. litura, S. omithogalli; Stigmella spp., Stomopteryx subsecivella, Strymon bazochii, Sylepta derogata, Synanthedon spp. such as S. exitiosa, Tecia solanivora, Telehin licus, Thaumatopoea pityocampa, Thaumatotibia (=Cryptophlebia) leucotreta, Thaumetopoea pityocampa, Theda spp., Theresimima ampelophaga, Thyrinteina spp, Tildenia inconspicuella, Tinea spp. such as T doacella, T pellionella; Tineola bisselliella, Tortrix spp. such as T viridana; Trichophaga tapetzella, Trichoplusia spp. such as T. ni; Tuta (=Scrobipalpula) absoluta, Udea spp. such as U.

rubigalis, U. rubigalis; Virachola spp., Yponomeuta padella, and Zeiraphera canadensis; insects from the order of Coleoptera, for example Acalymma vittatum, Acanthoscehdes obtectus, Adoretus spp., Agelastica alni, Agrilus spp. such as A. anxius, A. planipennis, A. sinuatus; Agriotes spp. such as A. fuscicollis, A. lineatus, A. obscurus; Alphitobius

diaperinus, Amphimallus solstitialis, Anisandrus dispar, Anisoplia austriaca, Anobium punctatum, Anomala corpulenta, Anomala rufocuprea, Anoplophora spp. such as A.

glabripennis; Anthonomus spp. such as A. eugenii, A. grandis, A. pomorum; Anthren us spp., Aphthona euphoridae, Apion spp., Apogonia spp., Athous haemorrhoidalis, Atomaria spp. such as A. linearis; Attagenus spp., Aulacophora femoralis, Blastophagus piniperda,

Blitophaga undata, Bruchidius obtectus, Bruchus spp. such as B. lentis, B. pisorum, B.

rufimanus; Byctiscus betulae, Callidiellum rufipenne, Callopistria floridensis, Callosobruchus chinensis, Cameraria ohridella, Cassida nebulosa, Cerotoma trifurcata, Cetonia aurata, Ceuthorhynchus spp. such as C. assimilis, C. napi; Chaetocnema tibialis, Cleonus mendicus, Conoderus spp. such as C. vespertinus; Conotrachelus nenuphar, Cosmopolites spp., Costelytra zealandica, Crioceris asparagi, Cryptolestes ferrugineus, Cryptorhynchus lapathi, Ctenicera spp. such as C. destructor; Curculio spp., Cylindrocopturus spp., Cyclocephala spp., Dactylispa balyi, Dectes texanus, Dermestes spp., Diabrotica spp. such as D.

undecimpunctata, D. speciosa, D. longicornis, D. semipunctata, D. virgifera; Diaprepes abbreviates, Dichocrocis spp., Dicladispa armigera, Diloboderus abderus, Diocalandra frumenti (Diocalandra stigmaticollis), Enaphalodes rufulus, Epilachna spp. such as E.

varivestis, E. vigintioctomaculata; Epitrix spp. such as E. hirtipennis, E. similaris; Eutheola humilis, Eutinobothrus brasiliensis, Faustinus cubae, Gibbium psylloides, Gnathocerus cornutus, Hellula undalis, Heteronychus arator, Hylamorpha elegans, Hylobius abietis, Hylotrupes bajulus, Hypera spp. such as H. brunneipennis, H. postica; Hypomeces squamosus, Hypothenemus spp., Ips typographus, Lachnosterna consanguinea, Lasioderma serricorne, Latheticus oryzae, Lathridius spp., Lema spp. such as L bilineata, L. melanopus; Leptinotarsa spp. such as L. decemlineata; Leptispa pygmaea, Limonius californicus, Lissorhoptrus oryzophilus, Lixus spp., Luperodes spp., Lyctus spp. such as L bruneus;

Liogenys fuscus, Macrodactylus spp. such as M. subspinosus; Maladera matrida,

Megaplatypus mutates, Megascelis spp., Melanotus communis, Meligethes spp. such as M. aeneus; Melolontha spp. such as M. hippocastani, M. melolontha; Metamasius hemipterus, Microtheca spp., Migdolus spp. such as M. fryanus, Monochamus spp. such as M.

alternatus; Naupactus xanthographus, Niptus hololeucus, Oberia brevis, Oemona hirta, Oryctes rhinoceros, Oryzaephilus surinamensis, Oryzaphagus oryzae, Otiorrhynchus sulcatus, Otiorrhynchus ovatus, Otiorrhynchus sulcatus, Oulema melanopus, Oulema oryzae, Oxycetonia jucunda, Phaedon spp. such as P. brassicae, P. cochleariae;

Phoracantha recurva, Phyllobius pyri, Phyllopertha horticola, Phyllophaga spp. such as P. helleri; Phyllotreta spp. such as P. chrysocephala, P. nemorum, P. striolata, P. vittula;

Phyllopertha horticola, Popillia japonica, Premnotrypes spp., Psacothea hilaris, Psylliodes chrysocephala, Prostephanus truncates, Psylliodes spp., Ptinus spp., Pulga saltona,

Rhizopertha dominica, Rhynchophorus spp. such as R. billineatus, R. ferrugineus, R.

palmarum, R. phoenicis, R. vulneratus; Saperda Candida, Scolytus schevyrewi,

Scyphophorus acupunctatus, Sitona lineatus, Sitophilus spp. such as S. granaria, S. oryzae, S. zeamais; Sphenophorus spp. such as S. tews; Stegobium paniceum, Sternechus spp. such as S. subsignatus; Strophomorphus ctenotus, Symphyletes spp., Tanymecus spp., Tenebrio molitor, Tenebrioides mauretanicus, Tribolium spp. such as T. castaneum;

Trogoderma spp., Tychius spp., Xylotrechus spp. such as X. pyrrhoderus; and, Zabrus spp. such as Z. tenebrioides;

insects from the order of Diptera for example Aedes spp. such as A. aegypti, A. albopictus, A. vexans; Anastrepha ludens, Anopheles spp. such as A. albimanus, A. crucians, A.

freeborni, A. gambiae, A. leucosphyrus, A. maculipennis, A. minimus, A. quadrimaculatus, A. sinensis; Bactrocera invadens, Bibio hortulanus, Calliphora erythrocephala, Calliphora vicina, Ceratitis capitata, Chrysomyia spp. such as C. bezziana, C. hominivorax, C. macellaria; Chrysops atlanticus, Chrysops discalis, Chrysops silacea, Cochliomyia spp. such as C.

hominivorax; Contarinia spp. such as C. sorghicola; Cordylobia anthropophaga, Culex spp. such as C. nigripalpus, C. pipiens, C. quinquefasciatus, C. tarsalis, C. tritaeniorhynchus; Culicoides furens, Culiseta inornata, Culiseta melanura, Cuterebra spp., Dacus cucurbitae, Dacus oleae, Dasineura brassicae, Dasineura oxycoccana, Delia spp. such as D. antique, D. coarctata, D. platura, D. radicum; Dermatobia hominis, Drosophila spp. such as D. suzukii, Fannia spp. such as F. canicularis; Gastraphilus spp. such as G. intestinalis; Geomyza tipunctata, Glossina spp. such as G. fuscipes, G. morsitans, G. palpalis, G. tachinoides; Haematobia irritans, Haplodiplosis equestris, Hippelates spp., Hylemyia spp. such as H. platura; Hypoderma spp. such as H. lineata; Hyppobosca spp., Hydrellia philippina,

Leptoconops torrens, Liriomyza spp. such as L. sativae, L trifolii; Lucilia spp. such as L caprina, L cuprina, L. sericata; Lycoria pectoralis, Mansonia titillanus, Mayetiola spp. such as M. destructor; Musca spp. such as M. autumnalis, M. domestica; Muscina stabulans, Oestrus spp. such as O. ovis; Opomyza florum, Oscinella spp. such as O. frit; Orseolia oryzae, Pegomya hysocyami, Phlebotomus argentipes, Phorbia spp. such as P. antiqua, P. brassicae, P. coarctata; Phytomyza gymnostoma, Prosimulium mixtum, Psila rosae,

Psorophora columbiae, Psorophora discolor, Rhagoletis spp. such as R. cerasi, R. cingulate, R. indifferens, R. mendax, R. pomonella; Rivellia quadrifasciata, Sarcophaga spp. such as S. haemorrhoidalis; Simulium vittatum, Sitodiplosis mosellana, Stomoxys spp. such as S.

calcitrans; Tabanus spp. such as T. atratus, T. bovinus, T. lineola, T. similis; Tannia spp., Thecodiplosis japonensis, Tipula oleracea, Tipula paludosa, and Wohlfahrtia spp;

insects from the order of Thysanoptera for example, Baliothrips biformis, Dichromothrips corbetti, Dichromothrips ssp., Echinothrips americanus, Enneothrips flavens, Frankliniella spp. such as F. fusca, F. occidentalis, F. tritici; Heliothrips spp., Hercinothrips femoralis, Kakothrips spp., Microcephalothrips abdominalis, Neohydatothrips samayunkur, Pezothrips kellyanus, Rhipiphorothrips cruentatus, Scirtothrips spp. such as S. citri, S. dorsalis, S. perseae; Stenchaetothrips spp, Taeniothrips cardamoni, Taeniothrips inconsequens, Thrips spp. such as T. imagines, T. hawaiiensis, T. oryzae, T. palmi, T. parvispinus, T. tabaci;

insects from the order of Hemiptera for example, Acizzia jamatonica, Acrosternum spp. such as A. hilare; Acyrthosipon spp. such as A. onobrychis, A. pisum; Adelges laricis, Adelges tsugae, Adelphocoris spp., such as A. rapidus, A. superbus; Aeneolamia spp., Agonoscena spp., Aulacorthum solani, Aleurocanthus woglumi, Aleurodes spp., Aleurodicus disperses, Aleurolobus barodensis, Aleurothrixus spp., Amrasca spp., Anasa tristis,

Antestiopsis spp., Anuraphis cardui, Aonidiella spp., Aphanostigma piri, Aphidula nasturtii, Aphis spp. such as A. craccivora, A. fabae, A. forbesi, A. gossypii, A. grossulariae, A.

maidiradicis, A. pomi, A. sambuci, A. schneideri, A. spiraecola; Arboridia apicalis, Arilus critatus, Aspidiella spp., Aspidiotus spp., Atanus spp., Aulacaspis yasumatsui, Aulacorthum solani, Bactericera cockerelli (Paratrioza cockerelli), Bemisia spp. such as B. argentifolii, B. tabaci (Aleurodes tabaci); Blissus spp. such as B. leucopterus; Brachycaudus spp. such as B. cardui, B. helichrysi, B. persicae, B. prunicola; Brachycolus spp., Brachycorynella asparagi, Brevicoryne brassicae, Cacopsylla spp. such as C. fulguralis, C. pyricola (Psylla piri); Calligypona marginata, Calocoris spp., Campylomma livida, Capitophorus horni, Carneocephala fulgida, Cavelerius spp., Ceraplastes spp., Ceratovacuna lanigera,

Ceroplastes ceriferus, Cerosipha gossypii, Chaetosiphon fragaefolii, Chionaspis tegalensis, Chlorita onukii, Chromaphis juglandicola, Chrysomphalus ficus, Cicadulina mbila, Cimex spp. such as C. hemipterus, C. lectularius; Coccomytilus halli, Coccus spp. such as C.

hesperidum, C. pseudomagnoliarum ; Corythucha arcuata, Creontiades dilutus, Cryptomyzus ribis, Chrysomphalus aonidum, Cryptomyzus ribis, Ctenarytaina spatulata, Cyrtopeltis notatus, Dalbulus spp., Dasynus piperis, Dialeurodes spp. such as D. citrifolii; Dalbulus maidis, Diaphorina spp. such as D. citri; Diaspis spp. such as D. bromeliae; Dichelops furcatus, Diconocoris hewetti, Doralis spp., Dreyfusia nordmannianae, Dreyfusia piceae, Drosicha spp., Dysaphis spp. such as D. plantaginea, D. pyri, D. radicola; Dysaulacorthum pseudosolani, Dysdercus spp. such as D. cingulatus, D. intermedius; Dysmicoccus spp., Edessa spp., Geocoris spp., Empoasca spp. such as E. fabae, E. solana; Epidiaspis leperii, Eriosoma spp. such as E. lanigerum, E. pyricola; Erythroneura spp., Eurygaster spp. such as E. integriceps; Euscelis bilobatus, Euschistus spp. such as E. heros, E. impictiventris, E. servus; Fiorinia theae, Geococcus coffeae, Glycaspis brimblecombei, Halyomorpha spp. such as H. halys; Heliopeltis spp., Homalodisca vitripennis (=H. coagulata), Horcias nobilellus, Hyalopterus pruni, Hyperomyzus lactucae, lcerya spp. such as I. purchase;

Idiocerus spp., Idioscopus spp., Laodelphax striatellus, Lecanium spp., Lecanoideus floccissimus, Lepidosaphes spp. such as L. ulmi; Leptocorisa spp., Leptoglossus phyllopus, Lipaphis erysimi, Lygus spp. such as L hesperus, L lineolaris, L pratensis; Maconellicoccus hirsutus, Marchalina hellenica, Macropes excavatus, Macrosiphum spp. such as M. rosae, M.

avenae, M. euphorbiae; Macrosteles quadrilineatus, Mahanarva fimbriolata, Megacopta cribraria, Megoura viciae, Melanaphis pyrarius, Melanaphis sacchari, Melanocallis

(=Tinocallis) caryaefoliae, Metcafiella spp., Metopolophium dirhodum, Monellia costalis, Monelliopsis pecanis, Myzocallis coryli, Murgantia spp., Myzus spp. such as M. ascalonicus, M. cerasi, M. nicotianae, M. persicae, M. varians; Nasonovia ribis-nigri, Neotoxoptera formosana, Neomegalotomus spp, Nephotettix spp. such as N. malayanus, N. nigropictus, N. parvus, N. virescens; Nezara spp. such as N. viridula; Nilaparvata lugens, Nysius huttoni, Oebalus spp. such as O. pugnax; Oncometopia spp., Orthezia praelonga, Oxycaraenus hyalinipennis, Parabemisia myricae, Parlatoria spp., Parthenolecanium spp. such as P. corni, P. persicae; Pemphigus spp. such as P. bursarius, P. populivenae; Peregrinus maidis, Perkinsiella saccharicida, Phenacoccus spp. such as P. aceris, P. gossypii; Phloeomyzus passerinii, Phorodon humuli, Phylloxera spp. such as P. devastatrix, Piesma quadrata, Piezodorus spp. such as P. guildinii; Pinnaspis aspidistrae, Planococcus spp. such as P. citri, P. ficus; Prosapia bicincta, Protopulvinaria pyriformis, Psallus seriatus, Pseudacysta persea, Pseudaulacaspis pentagona, Pseudococcus spp. such as P. comstocki; Psylla spp. such as P. mali; Pteromalus spp., Pulvinaria amygdali, Pyrilla spp., Quadraspidiotus spp., such as Q. perniciosus; Quesada gigas, Rastrococcus spp., Reduvius senilis, Rhizoecus americanus, Rhodnius spp., Rhopalomyzus ascalonicus, Rhopalosiphum spp. such as R.

pseudobrassicas, R. insertum, R. maidis, R. padi; Sagatodes spp., Sahlbergella singularis, Saissetia spp., Sappaphis mala, Sappaphis mali, Scaptocoris spp., Scaphoides titanus, Schizaphis graminum, Schizoneura lanuginosa, Scotinophora spp., Selenaspidus articulatus, Sitobion avenae, Sogata spp., Sogatella furcifera, Solubea insularis, Spissistilus festinus (=Stictocephala festina), Stephanitis nashi, Stephanitis pyrioides, Stephanitis takeyai, Tenalaphara malayensis, Tetraleurodes perseae, Therioaphis maculate, Thyanta spp. such as T. accerra, T. perditor; Tibraca spp., Tomaspis spp., Toxoptera spp. such as T. aurantii; Trialeurodes spp. such as T. abutilonea, T. ricini, T. vaporariorum; Triatoma spp., Trioza spp., Typhlocyba spp., Unaspis spp. such as U. citri, U. yanonensis; and Viteus vitifolii,

Insects from the order Hymenoptera for example Acanthomyops interjectus, Athalia rosae, Atta spp. such as A. capiguara, A. cephalotes, A. cephalotes, A. laevigata, A. robusta, A. sexdens, A. texana, Bombus spp., Brachymyrmex spp., Camponotus spp. such as C.

floridanus, C. pennsylvanicus, C. modoc; Cardiocondyla nuda, Chalibion sp, Crematogaster spp., Dasymutilla occidentalis, Diprion spp., Dolichovespula maculata, Dorymyrmex spp., Dryocosmus kuriphilus, Formica spp., Hoplocampa spp. such as H. minuta, H. testudinea; Iridomyrmex humilis, Lasius spp. such as L. niger, Linepithema humile, Liometopum spp., Leptocybe invasa, Monomorium spp. such as M. pharaonis, Monomorium, Nylandria fulva, Pachycondyla chinensis, Paratrechina longicornis, Paravespula spp., such as P. germanica, P. pennsylvanica, P. vulgaris; Pheidole spp. such as P. megacephala; Pogonomyrmex spp.

such as P. barbatus, P. californicus, Polistes rubiginosa, Prenolepis impairs, Pseudomyrmex gracilis, Schelipron spp., Si rex cyaneus, Solenopsis spp. such as S. geminata, S.invicta, S. molesta, S. richteri, S. xyloni, Sphecius speciosus, Sphex spp., Tapinoma spp. such as T. melanocephalum, T. sessile; Tetramorium spp. such as T. caespitum, T. bicarinatum, Vespa spp. such as V. crabro; Vespula spp. such as V. squamosal; Wasmannia auropunctata, Xylocopa sp;

Insects from the order Orthoptera for example Acheta domesticus, Calliptamus italicus, Chortoicetes terminifera, Ceuthophilus spp., Diastrammena asynamora, Dociostaurus maroccanus, Gryllotalpa spp. such as G. africana, G. gryllotalpa; Gryllus spp., Hieroglyph us daganensis, Kraussaria angulifera, Locusta spp. such as L. migratoria, L pardalina;

Melanoplus spp. such as M. bivittatus, M. femurrubrum, M. mexicanus, M. sanguinipes, M. spretus; Nomadacris septemfasciata, Oedaleus senegalensis, Scapteriscus spp.,

Schistocerca spp. such as S. americana, S. gregaria, Stemopelmatus spp., Tachycines asynamorus, and Zonozerus variegatus;

Pests from the Class Arachnida for example Acari,e.g. of the families Argasidae, Ixodidae and Sarcoptidae, such as Amblyomma spp. (e.g. A. americanum, A. variegatum, A.

maculatum), Argas spp. such as A. persicu), Boophilus spp. such as B. annulatus, B.

decoloratus, B. microplus, Dermacentor spp. such as D.silvarum, D. andersoni, D. variabilis, Hyalomma spp. such as H. truncatum, Ixodes spp. such as I. ricinus, I. rubicundus, I.

scapularis, I. holocyclus, I. pacificus, Rhipicephalus sanguineus, Ornithodorus spp. such as O. moubata, O. hermsi, O. turicata, Ornithonyssus bacoti, Otobius megnini, Dermanyssus gallinae, Psoroptes spp. such as P. ovis, Rhipicephalus spp. such as R. sanguineus, R. appendiculatus, Rhipicephalus evertsi, Rhizoglyphus spp., Sarcoptes spp. such asS.

Scabiei ; and Family Eriophyidae including Aceria spp. such as A. sheldoni, A. anthocoptes, Acallitus spp., Aculops spp. such as A. lycopersici, A. pelekassr, Aculus spp. such as A. schlechtendali; Colomerus vitis, Epitrimerus pyri, Phyllocoptruta oleivora; Eriophytes ribis and Eriophyes spp. such as Eriophyes sheldoni ; Family Tarsonemidae including

Hemitarsonemus spp., Phytonemus pallidus and Polyphagotarsonemus latus,

Stenotarsonemus spp. Steneotarsonemus spinkr', Family Tenuipalpidae including

Brevipalpus spp. such as B. phoenicis ; Family Tetranychidae including Eotetranychus spp., Eutetranychus spp., Oligonychus spp., Petrobia latens, Tetranychus spp. such as T.

cinnabarinus, T. evansi, T. kanzawai, T, pacificus, T. phaseulus, T. telarius and T. urticae ; Bryobia praetiosa ; Panonychus spp. such as P. ulmi, P. citrr', Metatetranychus spp. and Oligonychus spp. such as O. pratensis, O. perseae, Vasates lycopersici, Raoiella indica, Family Carpoglyphidae including Carpoglyphus spp.; Penthaleidae spp. such as Halotydeus destructor, Family Demodicidae with species such as Demodex spp.; Family Trombicidea including Trombicula spp.; Family Macronyssidae including Ornothonyssus spp.; Family

Pyemotidae including Pyemotes triticr, Tyrophagus putrescentiae\ Family Acaridae including Acarus s/'ro; Family Araneida including Latrodectus mactans, Tegenaria agrestis,

Chiracanthium sp, Lycosa sp Achaearanea tepidariorum and Loxosceles reclusa ;

Pests from the Phylum Nematoda, for example, plant parasitic nematodes such as root-knot nematodes, Meloidogyne spp. such as M. hapla, M. incognita, M. javanica; cyst-forming nematodes, Globodera spp. such as G. rostochiensis; Heterodera spp. such as H. avenae,

H. glycines, H. schachtii, H. trifolii; Seed gall nematodes, Anguina spp.; Stem and foliar nematodes, Aphelenchoides spp. such as A. besseyi; Sting nematodes, Belonolaimus spp. such as B. longicaudatus; Pine nematodes, Bursaphelenchus spp. such as B. lignicolus, B. xylophilus; Ring nematodes, Criconema spp., Criconemella spp. such as C. xenoplax and C. ornata; and, Criconemoides spp. such as Criconemoides informis; Mesocriconema spp.; Stem and bulb nematodes, Ditylenchus spp. such as D. destructor, D. dipsaci; Awl nematodes, Dolichodorus spp.; Spiral nematodes, Heliocotylenchus multicinctus; Sheath and sheathoid nematodes, Hemicycliophora spp. and Hemicriconemoides spp.; Hirshmanniella spp.; Lance nematodes, Hoploaimus spp.; False rootknot nematodes, Nacobbus spp.;

Needle nematodes, Longidorus spp. such as L. elongatus; Lesion nematodes, Pratylenchus spp. such as P. brachyurus, P. neglectus, P. penetrans, P. curvitatus, P. goodeyi; Burrowing nematodes, Radopholus spp. such as R. similis; Rhadopholus spp.; Rhodopholus spp.;

Reniform nematodes, Rotylenchus spp. such as R. robustus, R. reniformis; Scutellonema spp.; Stubby-root nematode, Trichodorus spp. such as T. obtusus, T. primitivus;

Paratrichodorus spp. such as P. minor; Stunt nematodes, Tylenchorhynchus spp. such as T. claytoni, T. dubius; Citrus nematodes, Tylenchulus spp. such as T. semipenetrans; Dagger nematodes, Xiphinema spp.; and other plant parasitic nematode species;

Insects from the order Isoptera for example Calotermes flavicollis, Coptotermes spp. such as C. formosanus, C. gestroi, C. acinaciformis; Cornitermes cumulans, Cryptotermes spp. such as C. brevis, C. cavifrons; Globitermes sulfureus, Heterotermes spp. such as H. aureus,

H. longiceps, H. tenuis; Leucotermes flavipes, Odontotermes spp., Incisitermes spp. such as

I. minor, I. Snyder, Marginitermes hubbardi, Mastotermes spp. such as M. darwiniensis Neocapritermes spp. such as N. opacus, N. parvus; Neotermes spp., Procornitermes spp., Zootermopsis spp. such as Z. angusticollis, Z. nevadensis, Reticulitermes spp. such as R. hesperus, R. tibialis, R. speratus, R. flavipes, R. grassei, R. lucifugus, R. santonensis, R. virginicus; Termes natalensis,

Insects from the order Blattaria for example Blatta spp. such as B. orientalis, B. lateralis; Blattella spp. such as B. asahinae, B. germanica; Leucophaea maderae, Panchlora nivea, Periplaneta spp. such as P. americana, P. australasiae, P. brunnea, P. fuligginosa, P.

japonica; Supella longipalpa, Parcoblatta pennsylvanica, Eurycotis floridana, Pycnoscelus surinamensis,

Insects from the order Siphonoptera for example Cediopsylla simples, Ceratophyllus spp., Ctenocephalides spp. such as C. felis, C. canis, Xenopsylla cheopis, Pulex irritans,

Trichodectes canis, Tunga penetrans, and Nosopsyllus fasciatus,

Insects from the order Thysanura for example Lepisma saccharina, Ctenolepisma urbana, and Thermobia domestica,

Pests from the class Chilopoda for example Geophilus spp., Scutigera spp. such as Scutigera coleoptrata,

Pests from the class Diplopoda for example Blaniulus guttulatus, Julus spp., Narceus spp., Pests from the class Symphyla for example Scutigerella immaculata,

Insects from the order Dermaptera, for example Forficula auricularia,

Insects from the order Collembola, for example Onychiurus spp., such as Onychiurus armatus,

Pests from the order Isopoda for example, Armadillidium vulgare, Oniscus asellus, Porcellio scaber,

Insects from the order Phthiraptera, for example Damalinia spp., Pediculus spp. such as Pediculus humanus capitis, Pediculus humanus corporis, Pediculus humanus humanus; Pthirus pubis, Haematopinus spp. such as Haematopinus eurysternus, Haematopinus suis ; Linognathus spp. such as Linognathus vituli; Bovicola bovis, Menopon gallinae,

Menacanthus stramineus and Solenopotes capillatus, Trichodectes spp.,

Examples of further pest species which may be controlled by compounds of fomula (I) include: from the Phylum Mollusca, class Bivalvia, for example, Dreissena spp.; class Gastropoda, for example, Arion spp., Biomphalaria spp., Bulinus spp., Deroceras spp., Galba spp., Lymnaea spp., Oncomelania spp., Pomacea canaliclata, Succinea spp.; from the class of the helminths, for example, Ancylostoma duodenale, Ancylostoma ceylanicum,

Acylostoma braziliensis, Ancylostoma spp., Ascaris lubricoides, Ascaris spp., Brugia malayi, Brugia timori, Bunostomum spp., Chabertia spp., Clonorchis spp., Cooperia spp.,

Dicrocoelium spp., Dictyocaulus filaria, Diphyllobothrium latum, Dracunculus medinensis, Echinococcus granulosus, Echinococcus multilocularis, Enterobius vermicularis, Faciola spp., Haemonchus spp. such as Haemonchus contortus; Heterakis spp., Hymenolepis nana, Hyostrongulus spp., Loa Loa, Nematodirus spp., Oesophagostomum spp., Opisthorchis spp., Onchocerca volvulus, Ostertagia spp., Paragonimus spp., Schistosomen spp., Strongyloides fuelleborni, Strongyloides stercora lis, Stronyloides spp., Taenia saginata, Taenia solium, Trichinella spiralis, Trichinella nativa, Trichinella britovi, Trichinella nelsoni, Trichinella pseudopsiralis, Trichostrongulus spp., Trichuris trichuria, Wuchereria bancrofti.

The compounds of the present invention are suitable for use in treating or protecting animals against infestation or infection by parasites. Therefore, the present invention also relates to the use of a compound of the present invention for the manufacture of a

medicament for the treatment or protection of animals against infestation or infection by parasites. Furthermore, the present invention relates to a method of treating or protecting animals against infestation and infection by parasites, which comprises orally, topically or parenterally administering or applying to the animals a parasiticidally effective amount of a compound of the present invention.

The present invention also relates to the non-therapeutic use of compounds of the present invention for treating or protecting animals against infestation and infection by parasites. Moreover, the present invention relates to a non-therapeutic method of treating or protecting animals against infestation and infection by parasites, which comprises applying to a locus a parasiticidally effective amount of a compound of the present invention.

The compounds of the present invention are further suitable for use in combating or controlling parasites in and on animals. Furthermore, the present invention relates to a method of combating or controlling parasites in and on animals, which comprises contacting the parasites with a parasitically effective amount of a compound of the present invention.

The present invention also relates to the non-therapeutic use of compounds of the present invention for controlling or combating parasites. Moreover, the present invention relates to a non-therapeutic method of combating or controlling parasites, which comprises applying to a locus a parasiticidally effective amount of a compound of the present invention.

The compounds of the present invention can be effective through both contact (via soil, glass, wall, bed net, carpet, blankets or animal parts) and ingestion (e.g. baits). Furthermore, the compounds of the present invention can be applied to any and all developmental stages.

The compounds of the present invention can be applied as such or in form of compositions comprising the compounds of the present invention.

The compounds of the present invention can also be applied together with a mixing partner, which acts against pathogenic parasites, e.g. with synthetic coccidiosis compounds, polyetherantibiotics such as Amprolium, Robenidin, Toltrazuril, Monensin, Salinomycin, Maduramicin, Lasalocid, Narasin or Semduramicin, or with other mixing partners as defined above, or in form of compositions comprising said mixtures.

The compounds of the present invention and compositions comprising them can be applied orally, parenterally or topically, e.g. dermally. The compounds of the present invention can be systemically or non-systemically effective.

The application can be carried out prophylactically, therapeutically or non-therapeutically. Furthermore, the application can be carried out preventively to places at which occurrence of the parasites is expected.

As used herein, the term "contacting" includes both direct contact (applying the

compounds/compositions directly on the parasite, including the application directly on the animal or excluding the application directly on the animal, e.g. at it's locus for the latter) and indirect contact (applying the compounds/compositions to the locus of the parasite). The contact of the parasite through application to its locus is an example of a non-therapeutic use of the compounds of the present invention.

The term "locus" means the habitat, food supply, breeding ground, area, material or environment in which a parasite is growing or may grow outside of the animal.

As used herein, the term“parasites” includes endo- and ectoparasites. In some

embodiments of the present invention, endoparasites can be preferred. In other

embodiments, ectoparasites can be preferred. Infestations in warm-blooded animals and fish include, but are not limited to, lice, biting lice, ticks, nasal bots, keds, biting flies, muscoid flies, flies, myiasitic fly larvae, chiggers, gnats, mosquitoes and fleas.

The compounds of the present invention are especially useful for combating parasites of the following orders and species, respectively:

fleas (Siphonaptera), e.g. Ctenocephalides felis, Ctenocephalides canis, Xenopsylla cheopis, Pulex irritans, Tunga penetrans, and Nosopsyllus fasciatus; cockroaches (Blattaria -Blattodea), e.g. Blattella germanica, Blattella asahinae, Periplaneta americana, Periplaneta japonica, Periplaneta brunnea, Periplaneta fuligginosa, Periplaneta australasiae, and Blatta orientalis; flies, mosquitoes (Diptera), e.g. Aedes aegypti, Aedes albopictus, Aedes vexans, Anastrepha ludens, Anopheles maculipennis, Anopheles crucians, Anopheles albimanus, Anopheles gambiae, Anopheles freeborni, Anopheles leucosphyrus, Anopheles minimus, Anopheles quadrimaculatus, Calliphora vicina, Chrysomya bezziana, Chrysomya

hominivorax, Chrysomya macellaria, Chrysops discalis, Chrysops silacea, Chrysops atlanticus, Cochliomyia hominivorax, Cordylobia anthropophaga, Culicoides furens, Culex pipiens, Culex nigripalpus, Culex quinquefasciatus, Culex tarsalis, Culiseta inornata, Culiseta melanura, Dermatobia hominis, Fannia canicularis, Gasterophilus intestinalis, Glossina morsitans, Glossina palpalis, Glossina fuscipes, Glossina tachinoides, Haematobia irritans, Haplodiplosis equestris, Hippelates spp., Hypoderma lineata, Leptoconops torrens, Lucilia caprina, Lucilia cuprina, Lucilia sericata, Lycoria pectoralis, Mansonia spp., Musca domestica, Muscina stabulans, Oestrus ovis, Phlebotomus argentipes, Psorophora columbiae, Psorophora discolor, Prosimulium mixtum, Sarcophaga haemorrhoidalis, Sarcophaga sp., Simulium vittatum, Stomoxys calcitrans, Tabanus bovinus, Tabanus atratus, Tabanus lineola, and Tabanus similis; lice (Phthiraptera), e.g. Pediculus humanus capitis, Pediculus humanus corporis, Pthirus pubis, Haematopinus eurysternus, Haematopinus suis, Linognathus vituli, Bovicola bovis, Menopon gallinae, Menacanthus stramineus and

Solenopotes capillatus; ticks and parasitic mites (Parasitiformes): ticks (Ixodida), e.g. Ixodes scapularis, Ixodes holocyclus, Ixodes pacificus, Rhiphicephalus sanguineus, Dermacentor andersoni, Dermacentor variabilis, Amblyomma americanum, Ambryomma maculatum, Ornithodorus hermsi, Ornithodorus turicata and parasitic mites (Mesostigmata), e.g.

Ornithonyssus bacoti and Dermanyssus gallinae ; Actinedida (Prostigmata) und Acaridida (Astigmata), e.g. Acarapis spp., Cheyletiella spp., Ornithocheyletia spp., Myobia spp., Psorergates spp., Demodex spp., Trombicula spp., Listrophorus spp., Acarus spp.,

Tyrophagus spp., Caloglyphus spp., Hypodectes spp., Pterolichus spp., Psoroptes spp., Chorioptes spp., Otodectes spp., Sarcoptes spp., Notoedres spp.,Knemidocoptes spp., Cytodites spp., and Laminosioptes spp; Bugs (Heteropterida): Cimex lectularius, Cimex hemipterus, Reduvius senilis, Triatoma spp., Rhodnius ssp., Panstrongylus ssp., and Arilus critatus; Anoplurida, e.g. Haematopinus spp., Linognathus spp., Pediculus spp., Phtirus spp., and Solenopotes spp.; Mallophagida (suborders Arnblycerina and Ischnocerina), e.g.

Trimenopon spp., Menopon spp., Trinoton spp., Bovicola spp., Werneckiella spp.,

Lepikentron spp., Trichodectes spp., and Felicola spp.; Roundworms Nematoda: Wipeworms and Trichinosis (Trichosyringida), e.g. Trichinellidae (Trichinella spp.), (Trichuridae) Trichuris spp., Capillaria spp.; Rhabditida, e.g. Rhabditis spp., Strongyloides spp., Helicephalobus spp.; Strongylida, e.g. Strongylus spp., Ancylostoma spp., Necator americanus,

Bunostomum spp. (Hookworm), Trichostrongylus spp., Haemonchus contortus, Ostertagia spp., Cooperia spp., Nematodirus spp., Dictyocaulus spp., Cyathostoma spp.,

Oesophagostomum spp., Stephanurus dentatus, Ollulanus spp., Chabertia spp.,

Stephanurus dentatus, Syngamus trachea, Ancylostoma spp., Uncinaria spp.,

Globocephalus spp., Necator spp., Metastrongylus spp., Muellerius capillaris,

Protostrongyius spp., Angiostrongylus spp., Parelaphostrongylus spp., Aleurostrongylus abstrusus, and Dioctophyma renale; Intestinal roundworms (Ascaridida), e.g. Ascaris lumbricoides, Ascaris suum, Ascaridia galli, Parascaris equorum, Enterobius vermicularis (Threadworm), Toxocara canis, Toxascaris leonine, Skrjabinema spp., and Oxyuris equi; Camallanida, e.g. Dracunculus medinensis (guinea worm); Spirurida, e.g. Thelazia spp., Wuchereria spp., Brugia spp., Onchocerca spp., Dirofilari spp. a, Dipetalonema spp., Setaria spp., Elaeophora spp., Spirocerca lupi, and Habronema spp.; Thorny headed worms

(Acanthocephala), e.g. Acanthocephalus spp., Macracanthorhynchus hirudinaceus and Oncicola spp.; Planarians (Plathelminthes): Flukes (Trematoda), e.g. Faciola spp.,

Fascioloides magna, Paragonimus spp., Dicrocoelium spp., Fasciolopsis buski, Clonorchis sinensis, Schistosoma spp., Trichobilharzia spp., Alaria alata, Paragonimus spp., and Nanocyetes spp., Cercomeromorpha, in particular Cestoda (Tapeworms), e.g.

Diphyllobothrium spp., Tenia spp., Echinococcus spp., Dipylidium caninum, Multiceps spp., Hymenolepis spp., Mesocestoides spp., Vampirolepis spp., Moniezia spp., Anoplocephala spp., Sirometra spp., Anoplocephala spp., and Hymenolepis spp..

As used herein, the term“animal” includes warm-blooded animals (including humans) and fish. Preferred are mammals, such as cattle, sheep, swine, camels, deer, horses, pigs, poultry, rabbits, goats, dogs and cats, water buffalo, donkeys, fallow deer and reindeer, and also in fur-bearing animals such as mink, chinchilla and raccoon, birds such as hens, geese, turkeys and ducks and fish such as fresh- and salt-water fish such as trout, carp and eels. Particularly preferred are domestic animals, such as dogs or cats.

In general, "parasiticidally effective amount" means the amount of active ingredient needed to achieve an observable effect on growth, including the effects of necrosis, death, retardation, prevention, and removal, destruction, or otherwise diminishing the occurrence and activity of the target organism. The parasiticidally effective amount can vary for the various compounds/compositions used in the invention. A parasiticidally effective amount of the compositions will also vary according to the prevailing conditions such as desired parasiticidal effect and duration, target species, mode of application, and the like.

Generally, it is favorable to apply the compounds of the present invention in total amounts of 0.5 mg/kg to 100 mg/kg per day, preferably 1 mg/kg to 50 mg/kg per day.

For oral administration to warm-blooded animals, the formula I compounds may be formulated as animal feeds, animal feed premixes, animal feed concentrates, pills, solutions, pastes, suspensions, drenches, gels, tablets, boluses and capsules. In addition, the formula I compounds may be administered to the animals in their drinking water. For oral

administration, the dosage form chosen should provide the animal with 0.01 mg/kg to 100 mg/kg of animal body weight per day of the formula I compound, preferably with 0.5 mg/kg to 100 mg/kg of animal body weight per day.

Alternatively, the formula I compounds may be administered to animals parenterally, for example, by intraruminal, intramuscular, intravenous or subcutaneous injection. The formula I compounds may be dispersed or dissolved in a physiologically acceptable carrier for subcutaneous injection. Alternatively, the formula I compounds may be formulated into an implant for subcutaneous administration. In addition the formula I compound may be transdermally administered to animals. For parenteral administration, the dosage form chosen should provide the animal with 0.01 mg/kg to 100 mg/kg of animal body weight per day of the formula I compound.

The formula I compounds may also be applied topically to the animals in the form of dips, dusts, powders, collars, medallions, sprays, shampoos, spot-on and pour-on formulations and in ointments or oil-in-water or water-in-oil emulsions. For topical application, dips and sprays usually contain 0.5 ppm to 5,000 ppm and preferably 1 ppm to 3,000 ppm of the formula I compound. In addition, the formula I compounds may be formulated as ear tags for animals, particularly quadrupeds such as cattle and sheep.

Suitable preparations are:

- Solutions such as oral solutions, concentrates for oral administration after dilution, solutions for use on the skin or in body cavities, pouring-on formulations, gels;

- Emulsions and suspensions for oral or dermal administration; semi-solid preparations; - Formulations wherein the active compound is processed in an ointment base or in an oil-in-water or water-in-oil emulsion base;

- Solid preparations such as powders, premixes or concentrates, granules, pellets, tablets, boluses, capsules; aerosols and inhalants, and active compound-containing shaped articles.

Compositions suitable for injection are prepared by dissolving the active ingredient in a suitable solvent and optionally adding further auxiliaries such as acids, bases, buffer salts, preservatives, and solubilizers. Suitable auxiliaries for injection solutions are known in the art. The solutions are filtered and filled sterile.

Oral solutions are administered directly. Concentrates are administered orally after prior dilution to the use concentration. Oral solutions and concentrates are prepared according to the state of the art and as described above for injection solutions, sterile procedures not being necessary.

Solutions for use on the skin are trickled on, spread on, rubbed in, sprinkled on or sprayed on. Solutions for use on the skin are prepared according to the state of the art and according to what is described above for injection solutions, sterile procedures not being necessary.

Gels are applied to or spread on the skin or introduced into body cavities. Gels are prepared by treating solutions which have been prepared as described in the case of the injection solutions with sufficient thickener that a clear material having an ointment-like consistency results. Suitable thickeners are known in the art.

Pour-on formulations are poured or sprayed onto limited areas of the skin, the active compound penetrating the skin and acting systemically. Pour-on formulations are prepared by dissolving, suspending or emulsifying the active compound in suitable skin-compatible solvents or solvent mixtures. If appropriate, other auxiliaries such as colorants,

bioabsorption-promoting substances, antioxidants, light stabilizers, adhesives are added. Suitable such auxiliaries are known in the art.

Emulsions can be administered orally, dermally or as injections. Emulsions are either of the water-in-oil type or of the oil-in-water type. They are prepared by dissolving the active compound either in the hydrophobic or in the hydrophilic phase and homogenizing this with the solvent of the other phase with the aid of suitable emulsifiers and, if appropriate, other auxiliaries such as colorants, absorption-promoting substances, preservatives, antioxidants, light stabilizers, viscosity-enhancing substances. Suitable hydrophobic phases (oils), suitable hydrophilic phases, suitable emulsifiers, and suitable further auxiliaries for emulsions are known in the art.

Suspensions can be administered orally or topically/dermally. They are prepared by suspending the active compound in a suspending agent, if appropriate with addition of other auxiliaries such as wetting agents, colorants, bioabsorption-promoting substances,

preservatives, antioxidants, light stabilizers. Suitable suspending agents, and suitable other auxiliaries for suspensions including wetting agents are known in the art.

Semi-solid preparations can be administered orally or topically/dermally. They differ from the suspensions and emulsions described above only by their higher viscosity.

For the production of solid preparations, the active compound is mixed with suitable excipients, if appropriate with addition of auxiliaries, and brought into the desired form.

Suitable auxiliaries for this purpose are known in the art.

The compositions which can be used in the invention can comprise generally from about 0.001 to 95% of the compound of the present invention.

Ready-to-use preparations contain the compounds acting against parasites, preferably ectoparasites, in concentrations of 10 ppm to 80 per cent by weight, preferably from 0.1 to 65 per cent by weight, more preferably from 1 to 50 per cent by weight, most preferably from 5 to 40 per cent by weight.

Preparations which are diluted before use contain the compounds acting against ectoparasites in concentrations of 0.5 to 90 per cent by weight, preferably of 1 to 50 per cent by weight.

Furthermore, the preparations comprise the compounds of formula I against endoparasites in concentrations of 10 ppm to 2 per cent by weight, preferably of 0.05 to 0.9 per cent by weight, very particularly preferably of 0.005 to 0.25 per cent by weight.

Topical application may be conducted with compound-containing shaped articles such as collars, medallions, ear tags, bands for fixing at body parts, and adhesive strips and foils.

Generally it is favorable to apply solid formulations which release compounds of the present invention in total amounts of 10 mg/kg to 300 mg/kg, preferably 20 mg/kg to 200 mg/kg, most preferably 25 mg/kg to 160 mg/kg body weight of the treated animal in the course of three weeks.

Examples:

With appropriate modification of the starting materials, the procedures as described in the preparation examples below were used to obtain further compounds of formula I. The compounds obtained in this manner are listed in the table that follows, together with physical data.

Compounds can be characterized e.g. by coupled High Performance Liquid

Chromatography /mass spectrometry (HPLC/MS), by 1H-NMR and/or by their melting points.

Analytical HPLC/MS - Method 1 : Agilent Eclipse Plus C18, 50 X 4,6 mm, ID 5pm; Elution: A = 10 mM Amm. Formate (0.1 % Formic Acid), B = Acetonitrile (0.1 % Formic Acid), Flow =

1.25 ml/min. at 40 °C; Gradient : 10 % B to 100 % B - 1.5 min, hold for 1 min, 1 min - 100% B. Run Time = 3.5 min.

Analytical HPLC/MS - Method 2: Kinetex XB C18 1 ,7m 50 x 2,1 mm; A = Water + 0.1 %

TFA, B = Acetonitrile, Flow = 0.8 ml/min - 1.0 ml/min in 1.5 min. at 60 °C; Gradient : 5 % B to 100 % B - 1.5 min.

1H-NMR: The signals are characterized by chemical shift (ppm, 5[delta]) vs.

tetramethylsilane respectively, CDC for 13C-NMR, by their multiplicity and by their integral (relative number of hydrogen atoms given). The following abbreviations are used to characterize the multiplicity of the signals: m = multiplet, h = heptet, q = quartet, t = triplet, d = doublet and s = singlet.

Abbreviations used are: d for day(s), h for hour(s), min for minute(s), r.t./room temperature for 20 - 25 °C, Rt for retention time; DMSO for dimethyl sulfoxide, OAc for acetate, EtOAc for ethyl acetate, THF for tetrahydrofuran, t-BuOH for tert-butanol, dppfPdCI for [1 ,1 -Bis(diphenylphosphino)ferrocene]dichloropalladium(ll), DIPEA for diisopropylethylamine,

DCM for dichloromethane and DMAP for 4-Dimethylaminopyridine

Preparation examples:

Example C-1 : 6-[(E)-[(2-isopropylphenyl)carbamothioylhydrazono]methyl]-N-[4-(trifluoromethoxy)phenyl]isoquinoline-1 -carboxamide (C-1 )

Step 1 : 6-bromo-N-[4-(trifluoromethoxy)phenyl]isoquinoline-1 -carboxamide

To a stirred solution of 6-bromoisoquinoline-1 -carboxylic acid (1.68 g) and 4-(trifluoromethoxy)aniline (1.2 g) in CH2CI2 (20 mL) were added EDCI (1.53 g) and DMAP (0.81 g) and the reaction mixture was stirred at r.t. for 16 h. An additional portion of and 4-(trifluoromethoxy)aniline (0.9 mL) and EDCI (0.2 g) were added and the reaction was stirred for an additional 20 h. The reaction mixture was then quenched with a solution of aq. HCI (1 M) then extracted with CFhCh. The organic phase was dried over MgS04, filtered and concentrated and used without further purification (2.5 g). LC/MS (method 1 ): Rt : 1.47 min; MS: m / z = 410 (M+).

Step 2: 6-[(E)-prop-1 -enyl]-N-[4-(trifluoromethoxy)phenyl]isoquinoline-1 -carboxamide A stirred suspension of 6-bromo-N-[4-(trifluoromethoxy)phenyl]isoquinoline-1 -carboxamide (2.5 g, 6.1 mmol), [(E)-prop-1-enyl]boronic acid (0.79 g), dppfPdCh (0.22 g), K2CO3 (1.69 g) in DME/H2O (25 mL, 2:1 ) was heated at 110°C for 16 h. The reaction mixture was allowed to cool to r.t. then extracted with EtOAc. The organic phase was dried over MgS04, filtered and concentrated. Purification by silica gel chromatography eluting with a gradient of CH/EE afforded the title compound (2.0 g). LC/MS (method 1 ): Rt : 1.54 min; MS: m / z = 373 (M+). Step 3: 6-formyl-N-[4-(trifluoromethoxy)phenyl]isoquinoline-1 -carboxamide

To a stirred solution of 6-[(E)-prop-1-enyl]-N-[4-(trifluoromethoxy)phenyl]isoquinoline-1-carboxamide (2.0 g) and OSO4 (1.3 mL, 2.5% in t-BuOH) in THF/H2O (80 mL, 1 :1 ) at 0°C was added Nal04 (2.3 g) and the reaction mixture was stirred from 0°C to r.t. over 16 h. The reaction mixture was then diluted with water and a saturated solution of NaS2C>3 (100 mL)

then extracted with EtOAc. The organic phase was dried over MgS04, filtered and concentrated and the resultant crude material was purified by trituration with diisopropyl ether to afford 6-formyl-N-[4-(trifluoromethoxy)phenyl]isoquinoline-1 -carboxamide (1 .55 g, 80% yield). LC/MS (method 1 ): Rt : 1.27 min; MS: m / z = 361 (M+).

Step 4: 6-[(E)-[(2-isopropylphenyl)carbamothioylhydrazono]methyl]-N-[4-(trifluoromethoxy)phenyl]isoquinoline-1 -carboxamide

A solution of 6-formyl-N-[4-(trifluoromethoxy)phenyl]isoquinoline-1 -carboxamide (1 .55 g) and 1 -amino-3-(2-isopropylphenyl)thiourea (1 .1 g) in EtOH (30 ml_) was stirred at 60°C for 4 h. The reaction mixture was then allowed to cool to r.t. and the crude product was isolated by filtration and purified by trituration with diisopropyl ether to afford 6-[(E)-[(2-isopropylphenyl)carbamothioylhydrazono]methyl]-N-[4-(trifluoromethoxy)phenyl]isoquinoline-1 -carboxamide (C-1 ) (1 .81 g, 76% yield). LC/MS (method 1 ): Rt : 1 .45 min; MS: m / z = 552 (M+). 1H NMR (400 MHz, THF-de) d 1 1.13 (s, 1 H), 10.66 (s, 1 H), 9.63 - 9.55 (m, 2H), 8.58 (d, J = 5.5 Hz, 1 H), 8.36 (dd, J = 9.2, 1 .7 Hz, 1 H), 8.18 (d, J = 2.6 Hz, 2H), 8.07 - 7.93 (m, 3H), 7.42 (dd, J = 7.8, 1.4 Hz, 1 H), 7.36 - 7.25 (m, 3H), 7.25 - 7.12 (m, 2H), 3.58 (dp, J =

2.3, 1.1 Hz, 6H), 3.26 (p, J = 6.9 Hz, 1 H), 2.51 (s, 4H), 1.72 (pt, J = 2.0, 0.9 Hz, 8H), 1.27 (d,

J = 6.9 Hz, 6H).

Example C-2: 6-[(E)-[(Z)-[3-(2-isopropylphenyl)-4-oxo-thiazolidin-2-ylidene]hydrazono]methyl]-N-[4-(trifluoromethoxy)phenyl]isoquinoline-1 -carboxamide:

A solution of 6-[(E)-[(2-isopropylphenyl)carbamothioylhydrazono]methyl]-N-[4-(trifluoromethoxy)phenyl]isoquinoline-1 -carboxamide (C-1 ) (1.65 g), methyl bromoacetate (0.59 mL) and NaOAc (0.98 g) in EtOH (100 mL) was stirred at 50°C for 16 h. The resultant precipate was isolated by filtration to afford 6-[(E)-[(Z)-[3-(2-isopropylphenyl)-4-oxo-thiazolidin-2-ylidene]hydrazono]methyl]-N-[4-(trifluoromethoxy)phenyl]isoquinoline-1 -carboxamide (1 .44 g, 81 % yield). LC/MS (method 1 ): Rt : 1.49 min; MS: m / z = 592 (M+). 1H NMR (400 MHz, THF-c/s) d 10.65 (s, 1 H), 9.60 (dd, J = 9.2, 0.9 Hz, 1 H), 8.57 (d, J = 5.5 Hz,

1 H), 8.24 (dd, J = 9.1 , 1.7 Hz, 1 H), 8.13 - 8.08 (m, 1 H), 8.07 - 7.96 (m, 3H), 7.50 - 7.37 (m, 2H), 7.28 (ddd, J = 14.8, 7.5, 1 .3 Hz, 3H), 7.16 (dd, J = 7.9, 1.3 Hz, 1 H), 4.14 - 3.99 (m, 2H), 3.57 (dq, J = 2.2, 1.1 Hz, 6H), 2.88 (hept, J = 6.9 Hz, 1 H), 2.51 (s, 5H), 1 .72 (ddp, J = 3.1 , 2.0, 1 .0 Hz, 8H), 1.20 (dd, J = 7.9, 6.9 Hz, 6H).




Biological examples

If not otherwise specified, the test solutions are prepared as follows:

The active compound is dissolved at the desired concentration in a mixture of 1 :1 (vokvol) distilled water : acetone. The test solution is prepared at the day of use.

Test solutions are prepared in general at concentrations of 1000 ppm, 500 ppm, 300 ppm, 100 ppm and 30 ppm (wt/vol).

B.1. Boll weevil ( Anthonomus grandis)

For evaluating control of boll weevil ( Anthonomus grandis) the test unit consisted of 96-well-microtiter plates containing an insect diet and 5-10 A. grandis eggs.

The compounds were formulated using a solution containing 75% v/v water and 25% v/v DMSO. Different concentrations of formulated compounds were sprayed onto the insect diet at 5 mI, using a custom built micro atomizer, at two replications.

After application, microtiter plates were incubated at about 25 + 1 °C and about 75 + 5 % relative humidity for 5 days. Egg and larval mortality was then visually assessed.

In this test, the following compounds at 800 ppm showed over 75% mortality in comparison with untreated controls: C-1 , C-2, C-3.

B.2. Diamond back moth ( Plutella xylostella)

The active compound is dissolved at the desired concentration in a mixture of 1 : 1 (vokvol) distilled water : acetone. Surfactant (Alkamuls® EL 620) is added at a rate of 0.1%

(vol/vol).The test solution is prepared at the day of use.

Leaves of cabbage were dipped in test solution and air-dried. Treated leaves were placed in petri dish enlined with moist filter paper and inoculated with ten 3rd instar larvae. Mortality was recorded 72 hours after treatment. Feeding damages were also recorded using a scale of 0-100%.

In this test, the following compounds at 300 ppm showed over 75% mortality in comparison with untreated controls: C-1 , C-2, C-3, C-4, C-6, C-8, C-9, C-10, C-1 1 , C-12, C-13, C-14.

B.3 Silverleaf whitefly ( Bemisia argentifolii) (adults)

The active compounds were formulated in cyclohexanone as a 10,000 ppm solution supplied in tubes. The tubes were inserted into an automated electrostatic sprayer equipped with an atomizing nozzle and they served as stock solutions for which lower dilutions were made in 50% acetone:50% water (v/v). A non-ionic surfactant (Kinetic®) was included in the solution at a volume of 0.01% (v/v).

Cotton plants at the cotyledon stage (one plant per pot) were sprayed by an automated electrostatic plant sprayer equipped with an atomizing spray nozzle. The plants were dried in the sprayer fume hood and then removed from the sprayer. Each pot was placed into a plastic cup and about 10 to 12 whitefly adults (approximately 3-5 days old) were introduced. The insects were collected using an aspirator and a nontoxic Tygon® tubing connected to a barrier pipette tip. The tip, containing the collected insects, was then gently inserted into the soil containing the treated plant, allowing insects to crawl out of the tip to reach the foliage for feeding. Cups were covered with a reusable screened lid. Test plants were maintained in a growth room at about 25°C and about 20-40% relative humidity for 3 days, avoiding direct exposure to fluorescent light (24-hour photoperiod) to prevent trapping of heat inside the cup. Mortality was assessed 3 days after treatment, compared to untreated control plants.

In this test, the following compounds at 300 ppm showed over 75% mortality in comparison with untreated controls: C-2.

B.4. Southern armyworm ( Spodoptera eridania), 2nd instar larvae

The active compounds were formulated in cyclohexanone as a 10,000 ppm solution supplied in tubes. The tubes were inserted into an automated electrostatic sprayer equipped with an atomizing nozzle and they served as stock solutions for which lower dilutions were made in 50% acetone:50% water (v/v). A nonionic surfactant (Kinetic®) was included in the solution at a volume of 0.01% (v/v).

Lima bean plants (variety Sieva) were grown 2 plants to a pot and selected for treatment at the 1st true leaf stage. Test solutions were sprayed onto the foliage by an automated electrostatic plant sprayer equipped with an atomizing spray nozzle. The plants were dried in the sprayer fume hood and then removed from the sprayer. Each pot was placed into perforated plastic bags with a zip closure. About 10 to 1 1 armyworm larvae were placed into the bag and the bags zipped closed. Test plants were maintained in a growth room at about 25°C and about 20-40% relative humidity for 4 days, avoiding direct exposure to fluorescent light (24 hour photoperiod) to prevent trapping of heat inside the bags. Mortality and reduced feeding were assessed 4 days after treatment, compared to untreated control plants.

In this test, the following compounds at 300 ppm showed over 75% mortality in comparison with untreated controls: C-1 , C-2.

B.5. Tobacco budworm ( Heliothis virescens)

For evaluating control of tobacco budworm ( Heliothis virescens) the test unit consisted of 96-well-microtiter plates containing an insect diet and 15-25 H. virescens eggs.

The compounds were formulated using a solution containing 75% v/v water and 25% v/v DMSO. Different concentrations of formulated compounds were sprayed onto the insect diet at 10 pi, using a custom built micro atomizer, at two replications.

After application, microtiter plates were incubated at about 28 + 1 °C and about 80 + 5 % relative humidity for 5 days. Egg and larval mortality was then visually assessed.

In this test, the following compounds at 800 ppm showed over 75% mortality in comparison with untreated controls: C-1 , C-2, C-3, C-6, C-7, C-8, C-9, C-10, C-1 1 , C-12, C-13, C-14.

B.6. Yellow fever mosquito (Aedes aegypti)

For evaluating control of yellow fever mosquito ( Aedes aegypti) the test unit consisted of 96-well-microtiter plates containing 200mI of tap water per well and 5-15 freshly hatched A. aegypti larvae. The active compounds were formulated using a solution containing 75% (v/v) water and 25% (v/v) DMSO. Different concentrations of formulated compounds or mixtures

were sprayed onto the insect diet at 2.5mI, using a custom built micro atomizer, at two replications.

After application, microtiter plates were incubated at 28 + 1 °C, 80 + 5 % RH for 2 days. Larval mortality was then visually assessed.

In this test, the following compounds at 800 ppm showed over 75% mortality in comparison with untreated controls: C-1 , C-2, C-9, C-10, C-11 , C-13, C-14.

B.7. Orchid thrips ( dichromothrips corbetti)

Dichromothrips corbetti adults used for bioassay were obtained from a colony maintained continuously under laboratory conditions. For testing purposes, the test compound is diluted in a 1 :1 mixture of acetone:water (vokvol), plus Kinetic® HV at a rate of 0.01 % v/v.

Thrips potency of each compound was evaluated by using a floral-immersion technique. All petals of individual, intact orchid flowers were dipped into treatment solution and allowed to dry in Petri dishes. Treated petals were placed into individual re-sealable plastic along with about 20 adult thrips. All test arenas were held under continuous light and a temperature of about 28°C for duration of the assay. After 3 days, the numbers of live thrips were counted on each petal. The percent mortality was recorded 72 hours after treatment.

In this test, the following compounds at 300 ppm showed over 75% mortality in comparison with untreated controls: C-1 , C-2, C-10, C-1 1 , C-12, C-13, C-14.

B.9. Western flower thrips (Frankliniella occidentalis)

The active compounds were formulated by a Tecan liquid handler in 100% cyclohexanone as a 10,000 ppm solution supplied in tubes. The 10,000 ppm solution was serially diluted in 100% cyclohexanone to make interim solutions. These served as stock solutions for which final dilutions were made by the Tecan in 50% acetone:50% water (v/v) into 10or 20ml glass vials. A nonionic surfactant (Kinetic®) was included in the solution at a volume of 0.01%

(v/v). The vials were then inserted into an automated electrostatic sprayer equipped with an atomizing nozzle for application to plants/insects.

Small (~2” in height) cotton plants are sprayed with test compounds at concentrations ranging from 300 to 0.01 ppm in acetone / water through the automated VPS. After drying, cotton leaves are removed and circular leaf discs (~1 cm diameter) are punched from the treated surface and transferred to clean 20 mL scintillation vials. Ten Western flower thrips (FRANOC) are aspirated into each scintillation vial. The vials with the leaf discs and thrips are kept in an upright incubator at 25°C and 50% relative humidity with a 14:10 lighhdark photoperiod. Each treatment is replicated twice.

Thrips mortality is assessed at 2 DAT (days after treatment), counting all thrips both dead and alive. [The average absolute mortality is calculated for each treatment.]

In this test, the following compounds at 300 ppm showed over 75% mortality in comparison with untreated controls: C-1 , C-2, C-10.