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.

公开(公告)号：DE59108229D1

公开(公告)日：1996-10-31

申请号：DE59108229

申请日：1991-12-10

Applicant: BASF AG

Inventor： WINGERT HORST DR ,  WOLF BERND DR ,  BENOIT REMY DR ,  SAUTER HUBERT DR ,  HEPP MICHAEL DR ,  GRAMMENOS WASSILIOS DR ,  KUEKENHOEHNER THOMAS DR

IPC: C07C69/736 ,  C07C20060101 ,  C07C51/09 ,  C07C51/367 ,  C07C59/68 ,  C07C65/21 ,  C07C65/24 ,  C07C67/22 ,  C07C69/738 ,  C07C69/76 ,  C07C235/34 ,  C07C235/78 ,  C07C249/08 ,  C07C251/48 ,  C07C253/14 ,  C07C255/17 ,  C07C255/40 ,  C07C317/24

Abstract: Prepn. of 2-phenoxymethyl benzoic acid derivs. of formula (I) comprises (a) converting a phenol of formula (II) to the phenolate in the presence of a basic diluent; (b) mixing the mixt. with a lactone of formula (III); (c) distilling off the diluent; (d) reacting the mixt. at 50-250 degrees C in the melt; and (e) dissolving the liq. melt with water and acidifying. X, Y = halogen, 1-4C alkyl, 1-4C alkoxy or CF3; m = 0-4; n = 0-3.

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

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

IPC: A01N37/50 ,  A01N43/40 ,  A01N43/84

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.

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.

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).

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

IPC: A01N47/04 ,  A01N37/50

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

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

IPC: A01N25/00 ,  A01N37/50 ,  A01N47/14

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.

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.)

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.)