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公开(公告)号:GR3019251T3
公开(公告)日:1996-06-30
申请号:GR960400648
申请日:1996-03-07
Applicant: BASF AG
Inventor: WINGERT HORST DR , SAUTER HUBERT DR , BENOIT REMY DR , ROEHL FRANZ DR , AMMERMANN EBERHARD DR , LORENZ GISELA DR
IPC: A01N37/36 , A01N37/38 , A01N37/50 , A01N43/08 , A01N43/16 , A01N43/40 , A01N43/42 , A01N43/58 , A01N57/22 , C07C69/734 , C07C69/738 , C07C251/48 , C07C255/15 , C07C255/23 , C07C255/31 , C07C255/35 , C07C255/37 , C07C255/54 , C07C255/62 , C07D203/10 , C07D205/04 , C07D207/325 , C07D213/30 , C07D213/57 , C07D213/61 , C07D213/69 , C07D215/22 , C07D239/26 , C07D307/60 , C07D309/12 , C07D309/36 , C07D309/38 , C07D309/40 , C07D311/46 , C07D311/54 , C07D311/62 , C07D335/02 , C07F9/40
Abstract: Benzyl enol ether derivatives of the formula I in which A denotes CH2, CHCl, CH-alkyl, CH-O-alkyl, CH-S-alkyl, N-O-alkyl and B denotes OH, alkoxy, alkylthio and alkylamino, U, V and W are identical or different and denote hydrogen, halogen, alkyl and alkoxy, R , R and R are identical or different and denote hydrogen, cyano, halogen, amino, ester, amide, acyl, S(O)nR , PO(OR )2, alkyl, haloalkyl, cycloalkyl, halocycloalkyl, cycloalkyl-alkyl, alkoxy-alkyl, alkylthio-alkyl, arylthio-alkyl, alkenyl, haloalkenyl, cycloalkenyl, halocycloalkenyl, alkynyl, alkoxy, haloalkoxy, alkylthio, benzylthio, alkylcarbonyl, optionally substituted phenylcarbonyl, optionally substituted benzylcarbonyl, alkoxycarbonyl, optionally substituted phenoxycarbonyl, optionally substituted benzyloxycarbonyl, optionally substituted aryl, optionally substituted aryloxy, optionally substituted arylthio, optionally substituted arylalkyl, optionally substituted arylalkenyl, optionally substituted aryloxyalkyl, optionally substituted arylthioalkyl, optionally substituted hetaryl, optionally substituted hetaryloxy, optionally substituted hetarylthio, optionally substituted heteroarylalkyl, optionally substituted hetarylalkenyl, optionally substituted hetaryloxyalkyl, optionally substituted heterocyclyl and optionally substituted heterocyclyloxy, and the radical R denotes hydrogen and C1-C4-alkyl, and R and R together and also R and R together can in each case form a carbocyclic or heterocyclic ring which, in turn, can be benzo-fused and substituted, and fungicides containing these compounds.
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公开(公告)号:AT138906T
公开(公告)日:1996-06-15
申请号:AT92101121
申请日:1992-01-24
Applicant: BASF AG
Inventor: GRAMMENOS WASSILIOS DR , HARREUS ALBRECHT DR , SAUTER HUBERT DR , HELLENDAHL BEATE DR , DOETZER REINHARD DR , AMMERMANN EBERHARD DR , LORENZ GISELA DR
IPC: A01N37/50 , A01N43/54 , A01N43/58 , A01N43/76 , A01N43/836 , C07C69/65 , C07C69/653 , C07C69/734 , C07C69/738 , C07C251/48 , C07C251/50 , C07C251/52 , C07C251/54 , C07C251/56 , C07C251/58 , C07C251/60 , C07C251/86 , C07C255/15 , C07C255/57 , C07C255/58 , C07C255/62 , C07D213/77 , C07D239/42 , C07D241/20 , C07D263/32 , C07D333/28
Abstract: Iminoalkyl-phenylacrylic acid derivs. (I) ar new: R = H or 1-6C alkyl; R = H; 1-4C alkyl opt. substd. by halo; or opt. substd. aryl; Z ,Z = H; halo; CN; NO2;etc.;Y = O; NH; or NR ; and R = H; 1-4C alkoxycarbonyl-1-4C alkyl; or opt. substd. alkyl, cycloalkyl, etc.; or Y+R form a ring which is opt. substd. when Y = NH or NR ; R = 1-6C alkyl; X = CH-1-4C alkoxy or CH-1-4C alkylthio (also 1-4C alkylidene and 1-4C alkoxyimino in the description).
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公开(公告)号:ES2085813T3
公开(公告)日:1996-06-01
申请号:ES94114506
申请日:1994-09-15
Applicant: BASF AG
Inventor: WINGERT HORST DR , SAUTER HUBERT DR , AMMERMANN EBERHARD DR , LORENZ GISELA DR , SAUR REINHOLD DR , SCHELBERGER KLAUS
Abstract: Fungicidal mixture comprising a) the oxime ether carboxamide of the formula I and b) a phthalimide derivative selected from the group consisting of the compounds II and III in a synergistically active amount.e
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公开(公告)号:ES2085811T3
公开(公告)日:1996-06-01
申请号:ES94114504
申请日:1994-09-15
Applicant: BASF AG
Inventor: WINGERT HORST DR , SAUTER HUBERT DR , AMMERMANN EBERHARD DR , LORENZ GISELA DR , SAUR REINHOLD DR , SCHELBERGER KLAUS
Abstract: Fungicidal mixture comprising a) the oxime ether carboxamide of the formula I and b) a dithiocarbamate (II) selected from the group consisting of - manganese ethylenebis(dithiocarbamate) (zinc complex) (IIa), - manganese ethylenebis(dithiocarbamate) (IIb), - zinc ammoniate ethylenebis(dithiocarbamate) (IIc) and - zinc ethylenebis(dithiocarbamate) (IId) in a synergistically active amount.
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公开(公告)号:AT136734T
公开(公告)日:1996-05-15
申请号:AT94114505
申请日:1994-09-15
Applicant: BASF AG
Inventor: WINGERT HORST DR , SAUTER HUBERT DR , AMMERMANN EBERHARD DR , LORENZ GISELA DR , SAUR REINHOLD DR , SCHELBERGER KLAUS , HAMPEL MANFRED DR
IPC: A01N37/50 , A01N43/653 , A01N47/38 , A01N55/00 , A01N55/10
Abstract: Fungicidal mixture comprising a) the oxime ether carboxamide of the formula I and b) an azole derivative II selected from the group consisting of the compounds II.1 to II.16 - 1-[(2RS,4RS; 2RS,4SR)-4-bromo-2-(2,4-dichlorophenyl)tetrahydrofuryl]-1H-1,2,4-triaz ole (II.1) - 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)-butan-2-ol (II.2) - (+/-)-4-chloro-4-[4-methyl-2-(1H-1,2,4-triazol-1-ylmethyl)-1,3-dioxolan- 2-yl]-phenyl 4-chlorophenyl ether (II.3) - (E)-(RS)-1-(2,4-dichlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl) pent-1-ene-3-ol (II.4) - (Z)-2-(1H-1,2,4-triazol-1-ylmethyl)-2-(4-fluorophenyl)-3-(2-chlorophen yl)-oxiran (II.5) - 4-(4-chlorophenyl)-2-phenyl-2-(1H-1,2,4-triazolylmethyl)-butyronitrile (II.6) - 3-(2,4-dichlorophenyl)-6-fluoro-2-(1H-1,2,4-triazol-1-yl)quinazolin-4( 3H)-one (II.7) - bis(4-fluorophenyl)(methyl)(1H-1,2,4-triazol-1-ylmethyl)silane (II.8) - (R,S)-2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)-hexan-2-ol (II.9) - (1RS,5RS;1RS,5SR)-5-(4-chlorobenzyl)-2,2-dimethyl-1-(1H- 1,2,4-triazol-1-ylmethyl)cyclopentanol (II.10) - N-propyl-N-[2-(2,4,6-trichlorophenoxy)ethyl]imidazole-1-carboxamide (II.11) - (+/-)-1-[2-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolan-2-ylmethyl]-1H-1,2 ,4-triazole (II.12) - (R,S)-1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)- pentan-3-ol (II.13) - (+/-)-2-(2,4-dichlorophenyl)-3-(1H-1,2,4-triazolyl)-propyl 1,1,2,2-tetrafluoroethyl ether (II.14) - (E)-1-[1-[[4-chloro-2-(trifluoromethyl)-phenyl]imino]-2-propoxyethyl]- 1H-imidazole (II.15) and - (RS)-2,4'-difluoro- alpha -(1H-1,2,4-triazol-1-ylmethyl)-benzhydryl-alcohol (II.16) in a synergistically active amount.)
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公开(公告)号:DK0645091T3
公开(公告)日:1996-05-13
申请号:DK94114505
申请日:1994-09-15
Applicant: BASF AG
Inventor: AMMERMANN EBERHARD DR , HAMPEL MANFRED DR , SAUR REINHOLD DR , SCHELBERGER KLAUS , WINGERT HORST DR , SAUTER HUBERT DR , LORENZ GISELA DR
IPC: A01N37/50 , A01N43/653 , A01N47/38 , A01N55/00 , A01N55/10
Abstract: Fungicidal mixture comprising a) the oxime ether carboxamide of the formula I and b) an azole derivative II selected from the group consisting of the compounds II.1 to II.16 - 1-[(2RS,4RS; 2RS,4SR)-4-bromo-2-(2,4-dichlorophenyl)tetrahydrofuryl]-1H-1,2,4-triaz ole (II.1) - 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)-butan-2-ol (II.2) - (+/-)-4-chloro-4-[4-methyl-2-(1H-1,2,4-triazol-1-ylmethyl)-1,3-dioxolan- 2-yl]-phenyl 4-chlorophenyl ether (II.3) - (E)-(RS)-1-(2,4-dichlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl) pent-1-ene-3-ol (II.4) - (Z)-2-(1H-1,2,4-triazol-1-ylmethyl)-2-(4-fluorophenyl)-3-(2-chlorophen yl)-oxiran (II.5) - 4-(4-chlorophenyl)-2-phenyl-2-(1H-1,2,4-triazolylmethyl)-butyronitrile (II.6) - 3-(2,4-dichlorophenyl)-6-fluoro-2-(1H-1,2,4-triazol-1-yl)quinazolin-4( 3H)-one (II.7) - bis(4-fluorophenyl)(methyl)(1H-1,2,4-triazol-1-ylmethyl)silane (II.8) - (R,S)-2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)-hexan-2-ol (II.9) - (1RS,5RS;1RS,5SR)-5-(4-chlorobenzyl)-2,2-dimethyl-1-(1H- 1,2,4-triazol-1-ylmethyl)cyclopentanol (II.10) - N-propyl-N-[2-(2,4,6-trichlorophenoxy)ethyl]imidazole-1-carboxamide (II.11) - (+/-)-1-[2-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolan-2-ylmethyl]-1H-1,2 ,4-triazole (II.12) - (R,S)-1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)- pentan-3-ol (II.13) - (+/-)-2-(2,4-dichlorophenyl)-3-(1H-1,2,4-triazolyl)-propyl 1,1,2,2-tetrafluoroethyl ether (II.14) - (E)-1-[1-[[4-chloro-2-(trifluoromethyl)-phenyl]imino]-2-propoxyethyl]- 1H-imidazole (II.15) and - (RS)-2,4'-difluoro- alpha -(1H-1,2,4-triazol-1-ylmethyl)-benzhydryl-alcohol (II.16) in a synergistically active amount.)
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公开(公告)号:DK0645089T3
公开(公告)日:1996-05-13
申请号:DK94114504
申请日:1994-09-15
Applicant: BASF AG
Inventor: SAUTER HUBERT DR , LORENZ GISELA DR , AMMERMANN EBERHARD DR , HAMPEL MANFRED DR , WINGERT HORST DR , SAUR REINHOLD DR , SCHELBERGER KLAUS
Abstract: Fungicidal mixture comprising a) the oxime ether carboxamide of the formula I and b) a dithiocarbamate (II) selected from the group consisting of - manganese ethylenebis(dithiocarbamate) (zinc complex) (IIa), - manganese ethylenebis(dithiocarbamate) (IIb), - zinc ammoniate ethylenebis(dithiocarbamate) (IIc) and - zinc ethylenebis(dithiocarbamate) (IId) in a synergistically active amount.
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公开(公告)号:DE4437496A1
公开(公告)日:1996-04-25
申请号:DE4437496
申请日:1994-10-20
Applicant: BASF AG
Inventor: WAGNER OLIVER DR , MUELLER THOMAS DR , AMMERMANN EBERHARD DR , LORENZ GISELA DR
IPC: A01N47/12 , A01N47/24 , C07C271/22 , C07C271/34 , C07C271/54 , C07C271/60 , C07C269/04 , C07C269/06
Abstract: Carbamoyl carboxylic acid amide derivs. of formula (I) and their salts are new. R1 = R or N=CW1W2; R = 1-8C alkyl, 2-8C alkenyl or 2-8C alkynyl, 3-7C cycloalkyl, 3-7C cycloalkenyl, A', aryl or heteroaryl (all opt. substd.), N=CW1W2; A' = a non-aromatic 4-8 membered ring (opt. contg. 1 or 2 heteroatoms); W1 = R; W2 = H or R; R2, R5 = H, 1-8C alkyl or 3-7C cycloalkyl (these last 2 gps. opt. partially or completely halogenated); R3 = 1-8C alkyl, 3-7C cycloalkyl, (opt. substd.); R4 = H or R3; or CR3R4 = A'; X = independently 1-8C alkyl, 2-8C alkenyl, 3-7C cycloalkyl and/or 3-7C cycloalkenyl (all opt. substd.) or H; m = 0-2; A = =CY1Y2; Y1 = 3-7C cycloalkyl or 3-7C cycloalkenyl (both opt. substd.); Y2 = 1-8C alkyl, 2-8C alkenyl or aryl (all opt. substd.), Y1 or H; R6 = aryl or heteroaryl (both opt. substd.)
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公开(公告)号:ES2083217T3
公开(公告)日:1996-04-01
申请号:ES93105924
申请日:1993-04-13
Applicant: BASF AG
Inventor: WINGERT HORST DR , SAUTER HUBERT DR , BENOIT REMY DR , ROEHL FRANZ DR , AMMERMANN EBERHARD DR , LORENZ GISELA DR
IPC: A01N37/36 , A01N37/38 , A01N37/50 , A01N43/08 , A01N43/16 , A01N43/40 , A01N43/42 , A01N43/58 , A01N57/22 , C07C69/734 , C07C69/738 , C07C251/48 , C07C255/15 , C07C255/23 , C07C255/31 , C07C255/35 , C07C255/37 , C07C255/54 , C07C255/62 , C07D203/10 , C07D205/04 , C07D207/325 , C07D213/30 , C07D213/57 , C07D213/61 , C07D213/69 , C07D215/22 , C07D239/26 , C07D307/60 , C07D309/12 , C07D309/36 , C07D309/38 , C07D309/40 , C07D311/46 , C07D311/54 , C07D311/62 , C07D335/02 , C07F9/40
Abstract: Benzyl enol ether derivatives of the formula I in which A denotes CH2, CHCl, CH-alkyl, CH-O-alkyl, CH-S-alkyl, N-O-alkyl and B denotes OH, alkoxy, alkylthio and alkylamino, U, V and W are identical or different and denote hydrogen, halogen, alkyl and alkoxy, R , R and R are identical or different and denote hydrogen, cyano, halogen, amino, ester, amide, acyl, S(O)nR , PO(OR )2, alkyl, haloalkyl, cycloalkyl, halocycloalkyl, cycloalkyl-alkyl, alkoxy-alkyl, alkylthio-alkyl, arylthio-alkyl, alkenyl, haloalkenyl, cycloalkenyl, halocycloalkenyl, alkynyl, alkoxy, haloalkoxy, alkylthio, benzylthio, alkylcarbonyl, optionally substituted phenylcarbonyl, optionally substituted benzylcarbonyl, alkoxycarbonyl, optionally substituted phenoxycarbonyl, optionally substituted benzyloxycarbonyl, optionally substituted aryl, optionally substituted aryloxy, optionally substituted arylthio, optionally substituted arylalkyl, optionally substituted arylalkenyl, optionally substituted aryloxyalkyl, optionally substituted arylthioalkyl, optionally substituted hetaryl, optionally substituted hetaryloxy, optionally substituted hetarylthio, optionally substituted heteroarylalkyl, optionally substituted hetarylalkenyl, optionally substituted hetaryloxyalkyl, optionally substituted heterocyclyl and optionally substituted heterocyclyloxy, and the radical R denotes hydrogen and C1-C4-alkyl, and R and R together and also R and R together can in each case form a carbocyclic or heterocyclic ring which, in turn, can be benzo-fused and substituted, and fungicides containing these compounds.
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公开(公告)号:GR3018484T3
公开(公告)日:1996-03-31
申请号:GR950403624
申请日:1995-12-20
Applicant: BASF AG
Inventor: WINGER HORST DR , SAUTER HUBERT DR , AMMERMANN EBERHARD DR , LORENZ GISELA DR
IPC: A01N47/06 , A01N47/10 , A01N47/12 , A01N47/14 , A01N47/18 , A01N47/20 , C07C251/40 , C07C251/48 , C07C271/12 , C07C271/28 , C07C329/00 , C07C329/02 , C07C329/04 , C07C329/12 , C07C329/14 , C07C329/16 , C07C329/20 , C07C333/04 , C07C333/14 , C07C333/20 , C07C333/22 , C07C333/24 , C07D213/40 , C07D213/75 , C07D317/58 , C07D317/64
Abstract: Benzyl derivatives of the formula I in which A denotes CH2, CHCl, CH-alkyl, CH-alkoxy, CH-alkylthio, N-alkoxy, B denotes OH, alkylthio, alkylamino, U, V and W denote hydrogen, halogen, alkyl or alkoxy, D denotes the group or where R' denotes hydrogen or alkyl and R denotes hydrogen, alkyl, cycloalkyl, haloalkyl, halocycloalkyl, cycloalkylalkyl, alkoxyalkyl, alkylthioalkyl, arylthioalkyl, aryloxyalkyl, aryl, arylalkyl, hetaryl, hetarylalky, hetaryloxyalkyl, heterocyclyl, and fungicides containing these compounds.
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