|1.||WO||WO/2005/048711 - COMBINATION OF ACTIVE SUBSTANCES WITH INSECTICIDAL PROPERTIES||02.06.2005||
|PCT/EP2004/012328||BAYER CROPSCIENCE AKTIENGESELLSCHAFT||FUNKE, Christian|
the invention relates to novel combinations of insecticidal active substances, containing compounds which are effective as insecticides on nicotinergic acetyl choline receptors as agonists and antagonists, and at least one active substance from the group of anthrilic acid amides, which are suitable for protecting plants against pests.
|2.||WO||WO/2005/048712 - ACTIVE AGENT COMBINATIONS WITH INSECTICIDAL AND ACARICIDAL PROPERTIES||02.06.2005||
|PCT/EP2004/012329||BAYER CROPSCIENCE AKTIENGESELLSCHAFT||FUNKE, Christian|
The invention relates to novel insecticidal agent combinations, comprising cyclic ketoenols or other acaricidal agents and further insecticidal agents, from the group of anthranilamides, which are particularly suitable for the prevention of animal pests such as insects and undesirable mites.
|3.||WO||WO/2005/047239 - PENTAFLUOROSULFANYL BENZOYLGUANIDINES, METHOD FOR THEIR PRODUCTION, THEIR USE AS MEDICAMENTS OR DIAGNOSTIC AGENTS AND MEDICAMENT CONTAINING THE SAME||26.05.2005||
|PCT/EP2004/012393||SANOFI-AVENTIS DEUTSCHLAND GMBH||KLEEMANN, Heinz-Werner|
The invention relates to pentafluorosulfanyl benzoylguanidines of formula (I), in which R1 to R4 are defined as cited in the claims. Said substances are suitable for use as anti-arrhythmic medicaments comprising cardio-protective components for the prophylaxis and treatment of infarcts, in addition to the treatment of angina pectoris. They also preventatively inhibit the pathophysiological events that occur during ischaemically induced traumas, in particular during the triggering of ischaemically induced cardiac arrhythmia.
|4.||WO||WO/2005/041653 - SYNERGISTIC FUNGICIDAL ACTIVE COMBINATIONS||12.05.2005||
|PCT/EP2004/011403||BAYER CROPSCIENCE AKTIENGESELLSCHAFT||WACHENDORFF-NEUMANN, Ulrike|
The novel active ingredient combinations made of a carboxamide of general formula (I) (group 1) (I) wherein A, R1 and R2 have the meaning cited in the description, and active ingredient groups (2) (24) which are disclosed in the description, have excellent fungicidal characteristics.
|5.||WO||WO/2005/037783 - USE OF TRICYCLIC COMPOUNDS AS GLYCINE TRANSPORT INHIBITORS||28.04.2005||
The invention relates to a compound having general formula (I), wherein: R represents a hydrogen atom or a vinyl group; n represents 0, 1 or 2; X represents a groups having formula CH or a nitrogen atom; R1 represents a phenyl or naphthyl group, or a cyclohexyl group, or a heteroaryl group; R2 represents a hydrogen atom, or one or more substituents selected from among the halogen atoms and the trifluoromethyl, alkyl, alkoxy, thienyl, phenyloxy, hydroxy, mercapto, thioalkyl, cyano groups or a group having general formula -NR4R5, SO2NR4R5, -SO2-alkyl, -SO2-phenyl, -CONR4R5, -COOR7, -CO-alkyl, -CO-phenyl, -NHCOR8, -NHSO2-alkyl, -NHSO2-phenyl and -NHSO2NR4R5 or a divalent group having formula -OCF2O-; and R4 and R5 each represent a hydrogen atom or an alkyl group or R4 and R5, together with the nitrogen atom bearing same, form a pyrrolidine, piperidine or morpholine ring. Compounds having formula (I) have a unique activity as specific inhibitors of glyt1 and/or glyt2 transporters.
|6.||WO||WO/2005/036966 - SYNERGISTIC INSECTICIDE MIXTURES||28.04.2005||
|PCT/EP2004/010912||BAYER CROPSCIENCE AKTIENGESELLSCHAFT||ANDERSCH, Wolfram|
The invention relates to insecticide mixtures respectively containing two compounds, as active ingredients, from the family of chloronicotinyl insecticides, and to the use of said mixtures for controlling animal parasites.
|7.||WO||WO/2005/034599 - A PROTECTIVE BOX-LIKE CABINET WITH COOLING ARRANGEMENTS||14.04.2005||
|PCT/SE2004/000932||ERIKSSON, Ulf, Jörgen||ERIKSSON, Ulf, Jörgen|
A protective shelter or cabinet related arrangement, wherein a first cabinet (10) is adapted to enclose electronic equipment (1a, 1b, 1c) which develops heat inside said first cabinet during operation, and a first air conditioning unit (11), adapted to regulate the temperature inside said first cabinet (10) and a standby battery assembly (2), wherein said standby battery assembly is enclosed in a further, a second, cabinet (20), whereby said further cabinet (20) is allotted a further, a second, air conditioning unit (21), each unit (11, 21) being adapted to regulate and keep the temperature within its related cabinet at a pre-selected level, and wherein said second air conditioning unit (21) is a thermo-electrically operated unit disposed with its cooling section (21a) facing towards said second cabinet (20) and with its heating section (21b) facing towards said first cabinet (10).
|8.||WO||WO/2005/028462 - DIMETHOXY DOCETAXEL ACETONE SOLVATE ET METHOD FOR THE PREPARATION THEREOF||31.03.2005||
|PCT/FR2004/002344||AVENTIS PHARMA S.A.||DIDIER, Eric|
The invention relates to dimethoxy docetaxel acetone solvate or (2R,3S)-3-tert-butoxycarbonylamino-2-hydroxy-3-phenyl-propionate of 4-acetoxy-2α-benzoyloxy-5?,20-epoxy-1-hydroxy-7β,10β-dimethoxy-9-oxo-tax-11-ene-13α-yle and to the preparation thereof by crystallisation from a hydro-acetone solution.
|9.||WO||WO/2005/028485 - SILICON COMPOUNDS WITH MICROBIOCIDAL ACTIVITY||31.03.2005||
|PCT/EP2004/010009||SYNGENTA PARTICIPATIONS AG||EHRENFREUND, Josef|
Fungicidal compounds of formula (I): where X is O or S; RING is phenyl or thienyl; Het is a 5- or 6-membered heterocyclic ring containing one to three heteroatoms, each independently selected from oxygen, nitrogen and sulphur, the ring being substituted by one to four groups R4 ; R1 is hydrogen, optionally substituted (C1-4)alkyl, formyl, optionally substituted (C1-4)alkylC(=O), optionally substituted (C1-4)alkylC(=O)O, optionally substituted (C1-4)alkoxy(C1-4)alkyl, optionally substituted allyl, optionally substituted propargyl or optionally substituted allenyl; each R2 is, independently, halogen, optionally substituted (C1-4)alkyl, optionally substituted (C1-4)alkoxy or optionally substituted (C1-4)alkoxy(C1-4)alkyl; R3 is (CRaRb)m_Cy-(CRCRd )n-Y; each R4 is, independently, selected from halogen, C1-3 alkyl, C1-3 haloalkyl, C1-3 alkoxy(C1-3)alkyl and cyano; Ra, Rb, Rc and Rd are each, independently, hydrogen or optionally substituted (C1-4)alkyl; Cy is an optionally substituted carbocyclic or heterocyclic 3-7 membered ring which may be saturated, unsaturated or aromatic and which optionally contains a silicon atom as a ring member; (CRaRb)m and (CRcRd)n may be bound either to the same carbon or silicon atom of Cy or to different atoms separated by 1, 2 or 3 ring members; Y is Si(OpZ1)(Oq Z2)(OsZ) and provided that Cy contains a silicon atom as a ring member then Y may also be hydrogen; Z is C1-4 alkyl or C2-4 alkenyl (each of which is optionally interrupted by one heteroatom selected from O, S and N and is optionally substituted by one to three independently selected halogen atoms); Z1 and Z2 are, independently, methyl or ethyl; in and n are each, independently, 0, 1, 2 or 3; p, q and s are each, independently, 0 or 1; and r is 0, 1 or 2; or an N-oxide thereof; novel intermediates used in the preparation of these compounds, agrochemical compositions which comprise at least one of the novel compounds as active ingredient and the use of the active ingredients or compositions in agriculture or horticulture for controlling or preventing infestation of plants by phytopathogenic microorganisms, preferably fungi.
|10.||WO||WO/2005/027638 - USE OF FUNGICIDES FOR DISINFECTING CEREAL SEED||31.03.2005||
|PCT/EP2004/009672||BAYER CROPSCIENCE AKTIENGESELLSCHAFT||SUTY-HEINZE, Anne|
The invention relates to the use of active ingredient combinations containing prothioconazole and tebuconazole, for disinfecting seed against an attack by phytopathogenic fungi.