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1. (WO1999005130) SUBSTITUTED 3-PHENYL ISOXAZOLINES
Latest bibliographic data on file with the International Bureau   

Pub. No.: WO/1999/005130 International Application No.: PCT/EP1998/004489
Publication Date: 04.02.1999 International Filing Date: 20.07.1998
Chapter 2 Demand Filed: 22.12.1998
IPC:
C07D 261/04 (2006.01)
Applicants: MENKE, Olaf[DE/DE]; DE (UsOnly)
MENGES, Markus[DE/DE]; DE (UsOnly)
HAMPRECHT, Gerhard[DE/DE]; DE (UsOnly)
REINHARD, Robert[DE/DE]; DE (UsOnly)
SCHÄFER, Peter[DE/DE]; DE (UsOnly)
ZAGAR, Cyrill[DE/DE]; DE (UsOnly)
WESTPHALEN, Karl-Otto[DE/DE]; DE (UsOnly)
MISSLITZ, Ulf[DE/DE]; DE (UsOnly)
WALTER, Helmut[DE/DE]; DE (UsOnly)
BASF AKTIENGESELLSCHAFT[DE/DE]; D-67056 Ludwigshafen, DE (AL, AM, AT, AU, AZ, BE, BG, BR, BY, CA, CH, CN, CY, CZ, DE, DK, ES, FI, FR, GB, GE, GR, HU, ID, IE, IL, IT, JP, KG, KR, KZ, LT, LU, LV, MC, MD, MX, NL, NO, NZ, PL, PT, RO, RU, SE, SG, SI, SK, TJ, TM, TR, UA)
Inventors: MENKE, Olaf; DE
MENGES, Markus; DE
HAMPRECHT, Gerhard; DE
REINHARD, Robert; DE
SCHÄFER, Peter; DE
ZAGAR, Cyrill; DE
WESTPHALEN, Karl-Otto; DE
MISSLITZ, Ulf; DE
WALTER, Helmut; DE
Agent: BASF AKTIENGESELLSCHAFT; D-67056 Ludwigshafen, DE
Common
Representative:
BASF AKTIENGESELLSCHAFT; D-67056 Ludwigshafen, DE
Priority Data:
197 31 513.523.07.1997DE
Title (EN) SUBSTITUTED 3-PHENYL ISOXAZOLINES
(FR) 3-PHENYLISOXAZOLINE SUBSTITUEE
(DE) SUBSTITUIERTE 3-PHENYLISOXAZOLINE
Abstract: front page image
(EN) The invention relates to substituted 3-phenyl isoxazolines of formula (I) and salts and enol ethers thereof, and to their use as herbicides. In said formula (I), X represents -O-, -S-, -N(R9)-; R1 represents CN, C1-C4alkyl, C1-C4alkyl halide, C1-C4halogen alkoxy, C1-C4alkyl sulfonyl; R2 represents H or optionally, substituted C1-C6 alkyl, (C1-C6 alkyl) carbonyl, C1-C6alkyl sulfonyl, C2-C6 alkenyl, (C2-C6 alkenyl) carbonyl, C2-C6alkinyl, (C2-C6alkinyl) carbonyl; R3 represents H, halogen; R4 represents CN, halogen, C1-C3 alkyl halide; R5 represents H, CN, halogen, C1-C3alkyl halide; R6 represents H, CN, halogen, C1-C3 alkyl halide or optionally, substituted C1-C6 alkoxy; R7 represents CN, halogen; R8 is at $g(a) when R7 is at $g(b), or at $g(b) when R7 is at $g(a) and represents: 1) H, OH, SH, CH, NO2, halogen, C1-C6alkyl, C1-C6alkyl halide, C1-C6halogen alkoxy, C1-C6 halogenalkylthio, C1-C6 alkylthio (C1-C6alkyl) carbonyl, (C1-C6 alkyl) iminooxycarbonyl, C1-C6alkoxy C1-C6alkyl, C1-C6alkoxyamino C1-C6alkyl, C1-C6alkoxy C1-C6alkylamino C1-C6alkyl, 2) optionally, substituted C1-C6alkoxy, C1-C6 alkylthio, C3-C6 cycloalkoxy, C3-C6 cycloalkylthio, C2-C6 alkenyloxy, C2-C6alkenylthio, C2-C6 alkinyloxy, C2-C6 alkinylthio, (C1-C6 alkyl) carbonyloxy, (C1-C6 alkyl) carbonylthio, (C1-C6 alkoxy) carboxyloxy, (C2-C6 alkenyl) carbonyloxy, (C2-C6 alkenyl) carbonylthio, (C2-C6 alkinyl) carbonyloxy, (C2-C6 alkinyl) carbonylthio, C1-C6 alkylsulfonyloxy or C1-C6 alkylsulfonyl and 3) 29 other radicals; and R9 represents H, C1-C6 alkyl, C3-C6 cycloalkyl, C3-C6 alkenyl, C3-C6 alkinyl, C1-C6 alkoxy C1-C6alkyl, (C3-C6 alkenyloxy) carbonyl C1-C6alkyl and optionally, substituted phenyl or phenyl C1-C6alkyl.
(FR) L'invention concerne des 3-phénylisoxazoline substituées représentés par la formule (I), ainsi que les sels et enoléthers de ces dernières, utilisés comme herbicides. Dans la formule (I), X = -O-, -S-, -N(R9)-; R1 = CN, alkyle C1-C4, halogénalkyle C1-C4, halogénalkoxy C1-C4, Alkylsulfonyle C1-C4; R2 = H ou éventuellement alkyle C1-C6, (alkyl C1-C6)carbonyle, alkylsulfonyle C1-C6, alcényle C2-C6, (alcényl C2-C6)carbonyle, alcynyle C2-C6, (alcynyl C2-C6)carbonyle; R3 = H, halogène; R4 = CN, halogène, halogénalkyle C1-C3; R5 = H, CN, halogène, halogénalkyle C1-C3, R6 = H, CN, halogène, halogénalkyle C1-C3 ou éventuellement alkoxy C1-C6 substitué; R7 = CN, halogène; R8 est en $g(a), lorsque R7 est en $g(b), ou R8 est en $g(b) lorsque R7 est en $g(a): 1) H, OH, SH, CN, NO2, halogène, alkyle C1-C6, halogénalkyle C1-C6, halogénalcoxy C1-C6, halogénalkylthio C1-C6, alkylthio C1-C6-(alkyl C1-C6)-carbonyle, (alkyl C1-C6)imino-oxycarbonyle, alcoxy C1-C6-alkyle C1-C6, alcoxy C1-C6-amino-alkyle C1-C6, alcoxy C1-C6-alkylamino-alkyle C1-C6, 2) éventuellement alcoxy C1-C6, alkylthio C1-C6, cycloalkoxy C3-C6, cycloalkylthio C3-C6, alcényloxy C2-C6, alcénylthio C2-C6, alcynyloxy C2-C6, alcynylthio C2-C6, (alkyl C1-C6)carbonyloxy, (alkyl C1-C6)carbonylthio, (alkoxy C1-C6)carboxyloxy, (alcényl C2-C6)carbonyloxy, (alcényl C2-C6)carbonylthio, (alcynyl C2-C6)carbonyloxy, (alcynyl C2-C6)carbonylthio, alkylsulfonyloxy C1-C6 ou Alkylsulfonyl C1-C6 substitués, 3) 29 groupes additionnels; R9 = H, alkyle C1-C6, cycloalkyle C3-C6, alcényle C3-C6, alcynyle C3-C6, alkoxy C1-C6-alkyle C1-C6, (alkoxy C1-C6)carbonyl-alkyle C1-C6, (alcényloxy C3-C6)carbonyle-alkyle C1-C6, éventuellement phényle substitué ou phényl-alkyle C1-C6.
(DE) Substituierte 3-Phenylisoxazoline der Formel (I), deren Salze und Enolether als Herbizide, wobei X = -O-, -S-, -N(R9)-; R1 = CN, C1-C4-Alkyl, C1-C4-Halogenalkyl, C1-C4-Halogenalkoxy, C1-C4-Alkylsulfonyl; R2 = H oder gegebenenfalls substituiertes C1-C6-Alkyl, (C1-C6-Alkyl)carbonyl, C1-C6-Alkylsulfonyl, C2-C6-Alkenyl, (C2-C6-Alkenyl)carbonyl, C2-C6-Alkinyl, (C2-C6-Alkinyl)-carbonyl; R3 = H, Halogen; R4 = CN, Halogen, C1-C3-Halogenalkyl; R5 = H, CN, Halogen, C1-C3-Halogenalkyl; R6 = H, CN, Halogen, C1-C3-Halogenalkyl oder gegebenenfalls subst. C1-C6-Alkoxy; R7 = CN, Halogen; R8 an $g(a), wobei R7 dann an $g(b) steht, oder an $g(b), wobei R7 dann an $g(a) steht; 1) H, OH, SH, CN, NO2, Halogen, C1-C6-Alkyl, C1-C6-Halogenalkyl, C1-C6-Halogenalkoxy, C1-C6-Halogenalkylthio, C1-C6-Alkylthio-(C1-C6-alkyl)-carbonyl, (C1-C6-Alkyl)iminooxycarbonyl, C1-C6-Alkoxy-C1-C6-alkyl, C1-C6-Alkoxyamino-C1-C6-alkyl, C1-C6-Alkoxy-C1-C6-alkylamino-C1-C6-alkyl, 2) gegebenenfalls substituiertes C1-C6-Alkoxy, C1-C6-Alkylthio, C3-C6-Cycloalkoxy, C3-C6-Cycloalkylthio, C2-C6-Alkenyloxy, C2-C6-Alkenylthio, C2-C6-Alkinyloxy, C2-C6-Alkinylthio, (C1-C6-Alkyl)carbonyloxy, (C1-C6-Alkyl)carbonylthio, (C1-C6-Alkoxy)carboxyloxy, (C2-C6-Alkenyl)carbonyloxy, (C2-C6-Alkenyl)carbonylthio, (C2-C6-Alkinyl)carbonyloxy, (C2-C6-Alkinyl)carbonylthio, C1-C6-Alkylsulfonyloxy oder C1-C6-Alkylsulfonyl, 3) 29 weitere Reste; R9 = H, C1-C6-Alkyl, C3-C6-Cycloalkyl, C3-C6-Alkenyl, C3-C6-Alkinyl, C1-C6-Alkoxy-C1-C6-alkyl, (C1-C6-Alkoxy)carbonyl-C1-C6-alkyl, (C3-C6-Alkenyloxy)carbonyl-C1-C6-alkyl, gegebenenfalls substituiertes Phenyl oder Phenyl-C1-C6-alkyl.
Designated States: AL, AU, BG, BR, BY, CA, CN, CZ, GE, HU, ID, IL, JP, KR, KZ, LT, LV, MX, NO, NZ, PL, RO, RU, SG, SI, SK, TR, UA, US
Eurasian Patent Office (AM, AZ, BY, KG, KZ, MD, RU, TJ, TM)
European Patent Office (EPO) (AT, BE, CH, CY, DE, DK, ES, FI, FR, GB, GR, IE, IT, LU, MC, NL, PT, SE)
Publication Language: German (DE)
Filing Language: German (DE)