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公开(公告)号:ES2098849T3
公开(公告)日:1997-05-01
申请号:ES94117414
申请日:1994-11-04
Applicant: BASF AG
Inventor: WAGNER OLIVER DR , EICKEN KARL DR , GOTZ NORBERT DR , RANG HARALD DR , AMMERMANN EBERHARD DR , LORENZ GISELA DR
IPC: A01N37/24 , A01N47/06 , A01N47/22 , A01N53/00 , C07C233/60 , C07C269/02 , C07C271/40 , C07C271/42 , C07C271/44 , C07C271/58
Abstract: p-Hydroxyaniline derivatives of the formula I in which the substituents have the following meanings: R is optionally substituted bicycloalkyl or bicycloalkenyl; R and R independently of one another are halogen, alkyl, haloalkyl, alkoxy and haloalkoxy; R is optionally substituted alkyl, alkenyl, cycloalkyl, cycloalkenyl or aryl, OR or NR R , where R is optionally substituted alkyl, alkenyl, cycloalkyl, cycloalkenyl or aryl, and R is hydrogen or alkyl, and salts thereof, processes for their preparation, compositions comprising them, and their use as fungicides or pesticides.
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公开(公告)号:AT149482T
公开(公告)日:1997-03-15
申请号:AT94117414
申请日:1994-11-04
Applicant: BASF AG
Inventor: WAGNER OLIVER DR , EICKEN KARL DR , GOETZ NORBERT DR , RANG HARALD DR , AMMERMANN EBERHARD DR , LORENZ GISELA DR
IPC: A01N37/24 , A01N47/06 , A01N47/22 , A01N53/00 , C07C233/60 , C07C269/02 , C07C271/40 , C07C271/42 , C07C271/44 , C07C271/58
Abstract: p-Hydroxyaniline derivatives of the formula I in which the substituents have the following meanings: R is optionally substituted bicycloalkyl or bicycloalkenyl; R and R independently of one another are halogen, alkyl, haloalkyl, alkoxy and haloalkoxy; R is optionally substituted alkyl, alkenyl, cycloalkyl, cycloalkenyl or aryl, OR or NR R , where R is optionally substituted alkyl, alkenyl, cycloalkyl, cycloalkenyl or aryl, and R is hydrogen or alkyl, and salts thereof, processes for their preparation, compositions comprising them, and their use as fungicides or pesticides.
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公开(公告)号:DE19531813A1
公开(公告)日:1997-03-06
申请号:DE19531813
申请日:1995-08-30
Applicant: BASF AG
Inventor: EICKEN KARL DR , RANG HARALD DR , HARREUS ALBRECHT DR , GOETZ NORBERT DR , AMMERMANN EBERHARD DR , LORENZ GISELA DR , STRATHMANN SIEGFRIED DR
IPC: A01N43/40 , A01N43/56 , A01N43/78 , C07D213/82 , C07D231/14 , C07D277/20 , C07D277/56 , C07D213/80 , A01N43/00
Abstract: The invention concerns biphenylamides of general formula (I) and their salts (A = (A1), (A2) or (A3); wherein R = F; R = H, halogen, alkyl, CF3, alkoxy, alkylthio; R = Cl, CF3; R = H, CH3; R = Cl, CH3, CHF2, CF3; R = CH3, CHF2, CF3). The invention also concerns agents containing (I), the preparation of (I) and these agents, and the use of both as fungicides.
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公开(公告)号:ES2094608T3
公开(公告)日:1997-01-16
申请号:ES94114509
申请日:1994-09-15
Applicant: BASF AG
Inventor: WINGERT HORST DR , MULLER BERND DR , SAUTER HUBERT DR , AMMERMANN EBERHARD DR , LORENZ GISELA DR , SAUR REINHOLD DR
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公开(公告)号:DK0648417T3
公开(公告)日:1996-12-23
申请号:DK94114509
申请日:1994-09-15
Applicant: BASF AG
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公开(公告)号:AT145789T
公开(公告)日:1996-12-15
申请号:AT94114509
申请日:1994-09-15
Applicant: BASF AG
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公开(公告)号:DK0513580T3
公开(公告)日:1996-11-18
申请号:DK92107059
申请日:1992-04-24
Applicant: BASF AG
Inventor: SAUTER HUBERT DR , ROEHL FRANZ DR , LORENZ GISELA DR , KUENAST CHRISTOPH DR , KIRSTGEN REINHARD DR , OTTER RAINER DR , GRAMMENOS WASSILIOS DR , OBERDORF KLAUS DR , AMMERMANN EBERHARD DR , KARDORFF UWE DR
IPC: A01N35/10 , A01N43/54 , A01N43/56 , A01N43/78 , C07C59/64 , C07C69/145 , C07C69/618 , C07C69/65 , C07C69/73 , C07C69/732 , C07C69/734 , C07C69/738 , C07C69/76 , C07C69/767 , C07C69/92 , C07C69/94 , C07C251/48 , C07C251/52 , C07C251/54 , C07C323/62 , C07D207/337 , C07D209/18 , C07D209/30 , C07D213/64 , C07D231/12 , C07D231/18 , C07D235/26 , C07D235/28 , C07D239/26 , C07D239/34 , C07D239/38 , C07D239/46 , C07D239/52 , C07D239/56 , C07D239/60 , C07D239/88 , C07D239/90 , C07D261/08 , C07D261/10 , C07D261/12 , C07D261/20 , C07D263/16 , C07D263/38 , C07D263/40 , C07D263/46 , C07D263/56 , C07D263/58 , C07D271/10 , C07D271/113 , C07D275/02 , C07D277/20 , C07D277/30 , C07D277/32 , C07D277/34 , C07D277/36 , C07D277/64 , C07D277/74 , C07D285/08 , C07D285/12 , C07D285/125 , C07D307/54 , C07D317/30 , C07D333/24 , C07F9/40
Abstract: alpha -Phenylacrylic acid derivatives I in which n = 0 to 4; y = 0 or 1; R = H; alkyl; alkenyl; alkynyl; optionally substituted cycloalkyl; vinyl or ethynyl if W represents a direct bond; R = CN; alkenyl; alkynyl; optionally substituted cycloalkyl; optionally substituted alkyl; R = H; NO2; CN; halogen; alkyl; alkoxy; haloalkyl; haloalkoxy; alkylthio; or, in the event that n represents 2, 3 or 4, two adjacent substituents R together are optionally substituted 1,3-butadiene-1,4-diyl; R = H; CHO; optionally substituted alkyl; optionally substituted alkenyl; optionally substituted alkynyl; an optionally substituted saturated or unsaturated cyclic radical; (phenyl)3P-; (phenyl)2PO-; (alkoxy)2PO-; an optionally substituted (hetero)aromatic system; W = a direct bond; oxygen; sulphur; optionally substituted nitrogen; A = -O-; -C(=O)-; -O-C(=O)-; -C(=O)-O-; -S-; -S(=O)-; -O-S(=0)--S(=O)-O-; -S(=O)2-; -O-S(=O)2-; -S(=O)2-O-; -NR -; -O-NR -; -NR -C(=O)-; -C(=O)-NR -; -NR -C(=O)-NR -; -NR -S(=O)-; -S(=O)-NR -; -NR -S-(=O)-NR -; -NR -S(=O)2-; -S(=O)2-NR -; -NR -S(=O)2-NR -; -N=N-; -NR -NR -; -NR -NR -C(=O)-; -C(=O)-NR -NR -; -NR -NR -S(=O)-; -S(=O)-NR -NR -; -NR -NR -S(=O)2-; -S(=O)2-NR -NR -; -O-(alkylene)-O-; -C-(=O)-(alkylene)-O-; -O-C(=O)-(alkylene)-O-; -C(=O)-O-(alkylene)-O-; -S-(alkylene)-O-; -S(=0)2-(alkylene)-O-; -O-S-(=O)2-(alkylene)-O-; -S(=O)2-O-(alkylene)-O-; -NR -(alkylene)-O-; -O-NR -(alkylene)-O-; -NR -C(=O)-(alkylene)-O-; -C(=O)-NR -(alkylene)-O-; -NR -C(=O)-NR -(alkylene)-O-; -N=N-(alkylene)-O-; -NR -NR -(alkylene)-O-; -NR -NR -C(=O)-(alkylene)-O-; -C(=O)-NR -NR -(alkylene)-O-; optionally substituted alkylene, alkenylene or alkynylene, it being possible for these carbon chains to be interrupted by one of the following groups or to be bonded to R or to the phenyl ring by one of the following groups: O, S, NR , CO, CO-O, O-CO, SO, SO2, SO2-O, O-SO2, NR -CO, CO-NR , NR -CO-NR , N=N, NR -NR , NR -NR -CO, CO-NR -NR ; R , R = H, alkyl or alkoxy, their preparation, fungicides and pesticides containing them, and their use.
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48.
公开(公告)号:CZ281522B6
公开(公告)日:1996-10-16
申请号:CS719589
申请日:1989-12-19
Applicant: BASF AG
Inventor: WINGERT HORST DR , SAUTER HUBERT DR , SCHUETZ FRANZ DR , WENDEROTH BERND DR , BRAND SIEGBERT DR , MUELLER BERND DR , ROEHL FRANZ DR , LORENZ GISELA DR , AMMERMANN EBERHARD DR
IPC: A01N37/10 , A01N37/38 , A01N41/10 , C07C317/46 , C07C323/56 , C07C323/62
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公开(公告)号:GR3019955T3
公开(公告)日:1996-08-31
申请号:GR960401322
申请日:1996-05-17
Applicant: BASF AG
Inventor: WINGERT HORST DR , SAUTER HUBERT DR , AMMERMANN EBERHARD DR , LORENZ GISELA DR , SAUR REINHOLD DR , SCHELBERGER KLAUS , HAMPEL MANFRED DR
Abstract: Fungicidal mixture, comprising a) the oxime ether carboxamide of the formula I and b) a morpholine derivative II selected from the group consisting of the compounds IIa, IIb and IIc in a synergistically active amount.
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公开(公告)号:DE4446458A1
公开(公告)日:1996-07-04
申请号:DE4446458
申请日:1994-12-27
Applicant: BASF AG
Inventor: WAGNER OLIVER DR , WETTERICH FRANK DR , EICKEN KARL DR , HARREUS ALBRECHT DR , AMMERMANN EBERHARD DR , LORENZ GISELA DR
IPC: C07C271/22 , C07C271/34 , C07C271/54 , C07C271/60 , A01N47/12 , C07C269/04 , C07C269/06
Abstract: Carbamoyl carboxylic acid amide derivs. of formula (I) and their salts are new R = 1-8C alkyl, 2-8C alkenyl, or 2-8C alkynyl (these gps. being opt. partially or completely halogenated and/or mono-, di- or tri-substd. with T gps.); 3-7C cycloalkyl or 3-7C cycloalkyl (these last 2 gps. being opt. partially or completely halogenated and/or mono-, di- or tri-substd. with T gps. (excluding cycloalkyl, cycloalkenyl and heteroaryl) or with 1-4C alkyl or aryl(1-4C)alkyl (this last gp. itself opt. substd. with T gps. excluding cycloalkyl or cycloalkenyl)); a non-aromatic 4-8 membered ring contg. in the ring, in addition to C, 1 or 2 heteroatoms chosen from O, S and N (the ring C being opt. mono-, di- or tri-substd. with halogen, 1-4C alkyl, T gps. (excluding cycloalkyl, cycloalkenyl and heteroaryl) and the second and any further N heteroatom carrying H or 1-4C alkyl); aryl or heteroaryl (these 2 gps. opt. mono-, di- or tri-substd. with halogen, 1-4C alkyl or T gps. (excluding cycloalkyl and cycloalkenyl)) or W W C=N; W = 1-8C alkyl (opt. partially or completely halogenated and/or opt. mono-, di- or tri-substd. with T gps. (excluding alkoxycarbonyl, cycloalkyl and cycloalkenyl)), 2-8C alkenyl, 2-8C alkynyl (opt. partially or completely halogenated and opt. mono-, di- or tri-substd. with 1-4C alkyl or T gps. (excluding cycloalkyl, cycloalkenyl and heteroaryl), 3-7C cycloalkyl or 3-7C cycloalkenyl (opt. mono-, di- or tri-substd. with halogen, 1-4C alkyl, aryl(1-4C)alkyl (this last gp. itself opt. substd. with halogen, 1-4C alkyl or T gps., excluding cycloalkyl, cycloalkenyl or heteroaryl) or T gps. (excluding cycloalkyl, cycloalkenyl, aryloxy or heteroaryl)), aryl or heteroaryl (these last 2 gps. opt. substd. with T gps., excluding cycloalkyl, cycloalkenyl or heteroaryl); W = H or a gp. W ; R = H, 1-8C alkyl or 3-7C cycloalkyl (these last 2 gps. opt. partially or completely halogenated); R = 1-8C alkyl, 3-7C cycloalkyl (opt. mono-, di- or tri-substd. with halogen, 1-4C alkyl, phenyl(1-4C)alkyl (in which the Ph gp. is opt. mono-, di- or tri-substd. with halogen, 1-4C alkyl or T gps., excluding cycloalkyl, cycloalkenyl, aryl, aryloxy or heteroaryl)); R = one of the R gps.; or R and R together with the C atom to which they are attached form a 4-8 membered ring which contains, in addition to C, 1 or 2 heteroatoms chosen from O, S and N (the ring C being opt. mono- or di-substd. with halogen, 1-4C alkyl and T gps. (excluding cycloalkyl, cycloalkenyl and heteroaryl) and the N heteroatom carrying H or 1-4C alkyl); R = a R gp.; X = H, 1-8C alkyl and/or 2-8C alkenyl (these last 2 gps. opt. partially or completely halogenated and opt. mono-, di- or tri-substd. with T gps., excluding cycloalkyl, cycloalkenyl or heteroaryl), 3-7C cycloalkyl and/or 3-7C cycloalkenyl (these 2 gps. opt. partially or completely halogenated and opt. mono-, di- or tri-substd. with 1-4C alkyl, aryl(1-4C) alkyl (this last opt. substd. with halogen, 1-4C alkyl and T gps., excluding cycloalkyl, cycloalkenyl and heteroaryl), or T gps. (excluding cycloalkyl, cycloalkenyl or heteroaryl)); m = 0-2; A = 3-7C cycloalkyl or 3-7C cycloalkenyl (opt. partially or completely halogenated and/or opt. mono-, di- or tri-substd. with 1-4C alkyl, aryl(1-4C)alkyl (thus last opt. mono-, di- or tri-substd. on aryl with halogen, 1-4C alkyl or T gps., excluding cycloalkyl, cycloalkenyl and heteroaryl) or T gps. excluding cycloalkyl, cycloalkenyl, aryloxy and heteroaryl); R = aryl or heteroaryl (these gps. opt. mono-, di- or tri-substd. with halogen or T gps., excluding cycloalkyl, cycloalkenyl or heteroaryl); T = CN, 1-4C alkoxyalkyl, 1-4C haloalkyl, 1-4C alkoxy, 1-4C haloalkoxy, 1-4C alkylthio, 1-4C alkoxycarbonyl, 3-7C cycloalkyl, 3-7C cycloalkenyl, aryl, aryloxy or heteroaryl, the cyclic gps. themselves being opt. mono-, di- or tri-substd. with halogen, CN, 1-4C alkyl, 1-4C alkoxy alkyl, 1-4C haloalkyl, 1-4C alkoxy, 1-4C haloalkoxy, 1-4C alkylthio, 1-4C alkoxycarbonyl, aryl, aryloxy or heteroaryl.
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