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    106.
    发明专利
    未知

    公开(公告)号：DE59507795D1

    公开(公告)日：2000-03-16

    申请号：DE59507795

    申请日：1995-09-19

    Applicant: BASF AG

    Inventor： KAST JUERGEN ,  VOSSEN MARCUS ,  VON DEYN WOLFGANG ,  ENGEL STEFAN ,  HILL LUISE ,  KARDORFF UWE ,  OTTEN MARTINA ,  PLATH PETER ,  WALTER HELMUT ,  WESTPHALEN KARL-OTTO ,  MISSLITZ ULF

    IPC: C07D317/26 ,  A01N33/18 ,  A01N33/26 ,  A01N35/02 ,  A01N35/06 ,  A01N41/10 ,  A01N43/28 ,  A01N43/32 ,  C07C49/84 ,  C07C69/757 ,  C07C69/76 ,  C07C201/12 ,  C07C205/45 ,  C07C245/08 ,  C07C255/66 ,  C07C309/04 ,  C07C311/02 ,  C07C317/24 ,  C07C323/22 ,  C07D317/14 ,  C07D319/06 ,  C07D339/06 ,  C07D339/08

    Abstract: PCT No. PCT/EP95/03685 Sec. 371 Date Mar. 18, 1997 Sec. 102(e) Date Mar. 18, 1997 PCT Filed Sep. 19, 1995 PCT Pub. No. WO96/10561 PCT Pub. Date Apr. 11, 19962- Aroylcyclohexanediones I where X, Y=O or S; Ar=phenyl or heteroaryl in each case having 1-4 substituents: halogen, cyano, nitro, -N=N-Ph, C1-C4-alkoxycarbonyl, -N(R9)-COR10, -N(R9)-SO2-R11, -SO2-N(R9)R10, -S(O)m-R8 or opt. subst. C1-C4-alkyl, C1-C4-alkoxy, C1-C4-haloalkyl or C1-C4-haloalkoxy; two adjacent C atoms of the phenyl or heteroaryl ring can also be bridged by means of a chain -C(R12)=C(R13)-C(R14)=C(R15)-, -Z1-C(R12)=N-, -Z1-N=C(R12)-, -Z1-C(R12)=C(R13)-, -Z1-C(R12)=C(R13)-C(R14,R15)-, -Z1-C (R12,R13)-C(R14,R15)-, -Z1-C(R12,R13)-C(R14R15)-Z2-, -C(R12,R13)-Z1-C(R14,R15)-C(R16,R17)-, -Z1-N(R20)-Z2-, -Z1-Z2-N(R20)-, -Z1-C(R12,R13)-Z2-N(R20)-, -Z1-N(R20)-Z2-N(R21)-, -N(R21)-Z1-Z2-, -N(R20)-Z1-N=C(R12)-, -Z1-C(R12,R13)-C(=NOR22)-, -Z1-C(R12,R13)-C(R14,R15)-C(=NOR22)- or Z1-Z2-Z1; (Z1, Z2=-O-, -S-, -SO-, -SO2-, -CO-, -C(R18,R19)- or -N(R20)-; R12, R19=H, OH, halogen, C1-C4alkyl, C1-C4-alkoxy, C1-C4-alkylthio, C1-C4-alkylamino, di-(C1-C4-alkyl)amino or phenyl; R20, R21=H, C1-C4-alkyl, C1-C4-alkoxy, C1-C4-alkylcarbonyl, phenyl or benzoyl; R22=H, C1-C4-alkyl, allyl or phenyl; Ph=phenyl, which can carry 1-3 substituents: halogen, cyano, nitro, -S(O)n-R23, C1-C4-alkoxycarbonyl, -SO2-N(R24)R25, -N(R24)-COR25, -N(R24)-SO2R26 or opt. subst. C1-C4-alkyl, C1-C4-alkoxy, C1-C4-haloalkyl or C1-C4-haloalkoxy; m, n=0-2; R8, R23=opt. subst. C1-C4-alkyl or C1-C4-haloalkyl; R9,R10,R24,R25=H, C1-C4-alkyl, C1-C4-haloalkyl or opt. subst. phenyl; R11, R26=opt. subst. C1-C4-alkyl or C1-C4-haloalkyl) R1,R2,R3,R4=hydrogen or C1-C4-alkyl; R5=H, C1-C4-alkyl or C1-C4-alkoxycarbonyl; R6, R7=C1-C4-alkyl, benzyl or together are an opt. subst. ethylene or propylene chain; excluding 2-(4-chloro-2-nitrobenzoyl)-5-dimethoxymethyl-5-methylcyclohexane-1,3-dione, and the salts of I and esters of I with acids. Use: herbicides; growth regulators.

    HETAROYL CYCLOHEXANEDIONE DERIVATIVES WITH HERBICIDAL EFFECT
    107.
    发明专利
    HETAROYL CYCLOHEXANEDIONE DERIVATIVES WITH HERBICIDAL EFFECT 未知

    公开(公告)号：SK26199A3

    公开(公告)日：2000-03-13

    申请号：SK26199

    申请日：1997-09-09

    Applicant: BASF AG

    Inventor： OTTEN MARTINA ,  GOETZ NORBERT ,  DEYN WOLFGANG VON ,  ENGEL STEFAN ,  KARDORFF UWE ,  PLATH PETER ,  HILL REGINA L ,  WITSCHEL MATTHIAS ,  MISSLITZ ULF ,  WESTPHALEN KARL-OTTO ,  WALTER HELMUT

    IPC: A01N43/42 ,  C07D215/14 ,  C07D215/18 ,  C07D215/22 ,  C07D215/233 ,  C07D215/26 ,  C07D215/36 ,  C07D215/48 ,  C07D215/60 ,  C07D217/02 ,  C07D217/08 ,  C07D217/22

    Abstract: Quinoline or isoquinoline derivatives of formula (Ia)-(Id) and their salts are new. R1, R2 = H, NO2, halo, CN, rhodano, OH, SH, 1-6C alkyl, 1-6C haloalkyl, 2-6C alkenyl, 2-6C alkynyl, 1-6C alkoxy, 1-6C haloalkoxy, 2-6C alkenyloxy, 2-6C alkynyloxy, 1-6C alkylthio, 1-6C haloalkylthio, 2-6C alkenylthio, 2-6C alkynylthio, 1-6C alkylsulphinyl, 1-6C haloalkylsulphinyl, 2-6C alkenylsulphinyl, 2-6C alkynylsulphinyl, 1-6C alkylsulphonyl, 1-6C haloalkylsulphonyl, 2-6C alkenylsulphonyl, 2-6C alkynylsulphonyl, 1-6C alkoxysulphonyl, 1-6C haloalkoxysulphonyl, 2-6C alkenyloxysulphonyl, 2-6C alkynyloxysulphonyl, Ar, OAr, SAr, SOAr or SO2Ar; Ar = phenyl (optionally fully or partially halogenated and substituted by 1 - 3 NO2, CN, OH, 1-4C alkyl, 1-4C haloalkyl, 1-4C alkoxy or 1-4C haloalkoxy); R3, R5, R7, R9 = NO2, CN, OH, SH, 2-4C alkenyl, 2-4C alkynyl, 2-4C alkenyloxy, 2-4C alkynyloxy, 2-4C alkenylthio, 2-4C alkynylthio, 1-4C alkylsulphinyl, 1-4C haloalkylsulphinyl, 2-4C alkenylsulphinyl, 2-4C alkynylsulphinyl, 1-4C alkylsulphonyl, 1-4C haloalkylsulphonyl, 2-4C alkenylsulphonyl, 2-4C alkynylsulphonyl, 1-4C alkoxysulphonyl, 1-4C haloalkoxysulphonyl, 2-4C alkenyloxysulphonyl, 2-4C alkynyloxysulphonyl, NR12R13, CO2R12, CONR12R13, Ar, OAr, SAr, SOAr or SO2Ar, or as for R4; R4, R6, R8, R10 = H, halo, 1-4C alkyl, 1-4C haloalkyl, 1-4C alkoxy, 1-4C haloalkoxy, 1-4C alkylthio or 1-4C haloalkylthio; or one CR3R4, CR5R6, CR7R8 or CR9R10 group = CO or C=NR13; or R4+R6, R6+R8 or R8+R10 = bond; R11 = H, 1-6C alkyl, 1-6C haloalkyl, 3-6C alkenyl, 3-6C alkynyl, 1-6C alkylcarbonyl, 1-6C haloalkylcarbonyl, CO2R12, CONR12R13 or SO2R12; or R4+R11, R6+R11 or R8+R11; R12 = H, 1-6C alkyl, 1-6C haloalkyl, 3-6C alkenyl, 3-6C alkynyl or Ar; R13 = 1-6C alkoxy, 1-6C haloalkoxy, 3-6C alkenyloxy, 3-6C alkynyloxy or as for R12; Q = 2,6-dioxo-cyclohexyl (optionally substituted).

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