42.
    发明专利
    未知

    公开(公告)号:BR9708047A

    公开(公告)日:1999-07-27

    申请号:BR9708047

    申请日:1997-03-06

    Applicant: BASF AG

    Abstract: The invention concerns a process for preparing nitrobiphenylene of formula (I) wherein m stands for 1 or 2, R means halogen, R' or OR', R' being a C-organic group which can carry groups which are inert in the reaction conditions, n stands for 0, 1, 2 or 3 and, if n is 2 or 3, the R groups can also be different. According to the invention, a chloronitrobenzene of formula (II) is reacted in the presence of a palladium catalyst and a base in a solvent with a phenyl boric acid (IIIa), one of its alkyl esters of formula (IIIb), R meaning C1-C6 alkyl, or one of its anhydrides. The compounds (I) are suitable as initial products for biphenylamines which are in turn intermediate products for fungicidal plant-growth substances.

    Substituted 3-phenyl isoxazolines
    46.
    发明专利

    公开(公告)号:AU8977398A

    公开(公告)日:1999-02-16

    申请号:AU8977398

    申请日:1998-07-20

    Applicant: BASF AG

    Abstract: PCT No. PCT/EP98/04489 Sec. 371 Date Jan. 21, 2000 Sec. 102(e) Date Jan. 21, 2000 PCT Filed Jul. 20, 1998 PCT Pub. No. WO99/05130 PCT Pub. Date Feb. 4, 1999Substituted 3-phenylisoxazolines I, and their salts and enol ethers, are described as herbicides where X=-O-, -S-, -N(R9)-; R1=CN, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-haloalkoxy, C1-C4-alkylsulfonyl; R2=H or unsubstituted or substituted C1-C6-alkyl, (C1-C6-alkyl)carbonyl, C1-C6-alkylsulfonyl, C2-C6-alkenyl, (C2-C6-alkenyl)carbonyl, C2-C6-alkynyl, (C2-C6-alkynyl)carbonyl; R3=H, halogen; R4=CN, halogen, C1-C3-haloalkyl; R5=H, CN, halogen, C1-C3-haloalkyl; R6=H, CN, halogen, C1-C3-haloalkyl or unsubstituted or substituted C1-C6-alkoxy; R7=CN, halogen; R8 in position alpha , R7 in this case being in position beta , or in position beta , R7 in this case being in position alpha , is 1) H, OH, SH, CN, NO2, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-haloalkoxy, C1-C6-haloalkylthio, 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) unsubstituted or substituted C1-C6-alkoxy, C1-C6-alkylthio, C3-C6-cycloalkoxy, C3-C6-cycloalkylthio, C2-C6-alkenyloxy, C2-C6-alkenylthio, C2-C6-alkynyloxy, C2-C6-alkynylthio, (C1-C6-alkyl)carbonyloxy, (C1-C6-alkyl)carbonylthio, (C1-C6-alkoxy)carboxyloxy, (C2-C6-alkenyl)carbonyloxy, (C2-C6-alkenyl)carbonylthio, (C2-C6-alkynyl)carbonyloxy, (C2-C6-alkynyl)carbonylthio, C1-C6-alkylsulfonyloxy or C1-C6-alkylsulfonyl, 3) 29 further radicals; R9=H, C1-C6-alkyl, C3-C6-cycloalkyl, C3-C6-alkenyl, C3-C6-alkynyl, C1-C6-alkoxy-C1-C6-alkyl, (C1-C6-alkoxy)carbonyl-C1-C6-alkyl, (C3-C6-alkenyloxy)carbonyl-C1-C6-alkyl, unsubstituted or substituted phenyl or phenyl-C1-C6-alkyl.

    Substituted 2-benz(o)ylpyridines, their preparation and their use as herbicides

    公开(公告)号:AU6829298A

    公开(公告)日:1998-10-20

    申请号:AU6829298

    申请日:1998-03-09

    Applicant: BASF AG

    Abstract: Substituted 2-benz(o)ylpyridines Iand salts thereof wheren=0, 1;X=CO, CH2, CH(C1-C4-alkyl), CH-OH, CH-CN, CH-halogen, C(halogen)2, CH-CONH2, CH-CO-O(C1-C4-alkyl), CH-O(C1-C4-alkyl), C(CN)(C1-C4-alkyl);R1=halogen, C1-C4-haloalkyl, C1-C4-alkylthio, C1-C4-alkylsulfinyl, C1-C4-alkylsulfonyl;R2=H, halogen;R3=H, NO2, OH, halogen, C1-C4-alkoxy;R4=H, NO2, OH, halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy;R5=H, NO2, CN, halogen, C1-C8-alkyl, C3-C8-alkenyl, C3-C8-alkynyl, C3-C8-cycloalkyl, C1-C8-haloalkyl, C2-C8-haloalkenyl, C2-C8-haloalkinyl, C1-C4-alkoxy-C1-C4-alkyl, C2-C4-alkenyloxy-C1-C4-alkyl, C2-C4-alkynyloxy-C1-C4-alkyl, C1-C4-alkylthio-C1-C4-alkyl, C1-C4-alkylsulfinyl-C1-C4-alkyl, C1-C4-alkylsulfonyl-C1-C4-alkyl, cyano-C1-C8-alkyl, cyano-C2-C8-alkenyl, cyano-C3-C8-alkynyl, unsubstituted or substituted OH, SH, SO-H, -SO2-H, COOH or NH-COOH, -SO2Cl, -N(R9,R10), -NH-SO2-(C1-C8-alkyl), -N[-SO2-(C1-C8-alkyl)]2, -N(C1-C8-alkyl)[-SO2-(C1-C8-alkyl)], -SO2-N(R9,R10), -O-CO-NH-R9, unsubstituted or substituted CHO, -O-CHO or -NH-CHO, -NH-CO-NH-R9, -O-CS-NH2, -O-CS-N(C1-

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