公开(公告)号：KR840001108B1

公开(公告)日：1984-08-06

申请号：KR840002417

申请日：1984-05-03

Applicant: BASF AG

Inventor： ZEEH BERND ,  AMMERMAN EBERHARD ,  POMMER ERNST-HEINRICH ,  GOETY NORBERT

IPC: C07D249/08 ,  C07D233/60

公开(公告)号：KR840001136B1

公开(公告)日：1984-08-09

申请号：KR800002535

申请日：1980-06-27

Applicant: BASF AG

Inventor： ZEEH BERND ,  AMMERMAN EBERHARD ,  HEINRICH POMMER ERNST ,  GOETZ NORBERT

IPC: C07D249/08 ,  C07D233/60

公开(公告)号：WO0195721A3

公开(公告)日：2002-04-25

申请号：PCT/EP0106686

申请日：2001-06-13

Applicant: BASF AG ,  GRAMMENOS WASILIOS ,  SAUTER HUBERT ,  CULLMANN OLIVER ,  GEWEHR MARKUS ,  MUELLER BERND ,  TORMO I BLASCO JORDI ,  GOETZ NORBERT ,  VOLK THORSTEN ,  LORENZ GISELA ,  AMMERMANN EBERHARD ,  STIERL REINHARD ,  STRATHMANN SIEGFRIED

Inventor： GRAMMENOS WASILIOS ,  SAUTER HUBERT ,  CULLMANN OLIVER ,  GEWEHR MARKUS ,  MUELLER BERND ,  TORMO I BLASCO JORDI ,  GOETZ NORBERT ,  VOLK THORSTEN ,  LORENZ GISELA ,  AMMERMAN EBERHARD ,  STIERL REINHARD ,  STRATHMANN SIGFRIED

IPC: A01N37/18 ,  A01N37/36 ,  A01N37/38 ,  C07C231/02 ,  C07C233/22 ,  C07C233/69

CPC classification number: A01N37/36 ,  A01N37/18 ,  A01N37/38 ,  C07C231/02 ,  C07C233/22

Abstract: The invention relates to the use of phenethyl acrylamides of formula (I) for controlling phytopathogenic fungi, wherein the substituents of said phenethyl acrylamides have the following significations: X signifies halogen, alkyl, halogenalkyl, alkoxy halogenalkoxy and -O-C(Ra, Rb)-C C-R?6; Ra, Rb and Rc¿ have the signification given in the description; m, n independently signify 1 to 4, the radicals X or Y being potentially different if m or n is higher than 1; Y signifies halogen, nitro, cyano, alkyl, CF¿3?, alkoxy and phenyl; R?1, R2¿ independently signify hydrogen, halogen, alkyl, alkoxy, halogenalkoxy and CF¿3?; R?3, R4, R5, and R6¿ independently signify hydrogen, alkyl and alkoxy, or R?3 and R4¿ together form a cyclopropyl ring, whereby the C-R5 and C-R6 bonds can be in position E or Z in relation to each other. The invention also relates to novel phenethyl acrylamides, a method for the production thereof, and agents containing the same.

公开(公告)号：ZA9606370B

公开(公告)日：1998-03-20

申请号：ZA9606370

申请日：1996-07-26

Applicant: BASF AG

Inventor： MUELLER RUTH ,  BAYER HERBERT ,  SAUTER HUBERT ,  HARREUS ALBRECHT ,  MUELLER BERND ,  STRATHMANN SIEGFRIED ,  LORENZ GISELA ,  AMMERMAN EBERHARD ,  HARRIES VOLKER ,  GOETZ NORBERT ,  GROTE THOMAS

IPC: A01N20060101 ,  C07C20060101 ,  C07D20060101 ,  C07C ,  A01N ,  C07D

公开(公告)号：EA003136B1

公开(公告)日：2003-02-27

申请号：EA200000676

申请日：1998-12-15

Applicant: BASF AG

Inventor： SCHELBERGER KLAUS ,  SCHERER MARIA ,  EICKEN KARL ,  HAMPEL MANFRED ,  AMMERMAN EBERHARD ,  LORENZ GISELLA

IPC: A01N37/22 ,  A01N37/24 ,  A01N43/08 ,  A01N43/16 ,  A01N43/32 ,  A01N43/40 ,  A01N43/56 ,  A01N43/653 ,  A01N43/76 ,  A01N43/78 ,  A01N47/38 ,  A01N55/00 ,  A01N43/50

Abstract: Визобретенииописанафунгициднаясмесь, содержащаяв качествеактивныхкомпонентова) амидноесоединениеформулы Iбгде RозначаетгалогениRозначаетфенил, замещенныйгалогеном; иб) производноеазолов II, выбранноеизгруппы, включающейсоединения II.1-II.17:1-[(2RS,4RS;2RS,4SR)-4-бром-2-(2,4-дихлорфенил)тетрагидрофурил]-1Н-1,2,4-триазол (II.1);2-(4-хлорфенил)-3-циклопропил-1-(1Н-1,2,4-триазол-1-ил)бутан-2-ол (II.2);(±)-4-хлор-4-[4-метил-2-(1Н-1,2,4-триазол-1-илметил)-1,3-диоксолан-2-ил]фенил-4-хлорфениловыйэфир (II.3);(Е)-(R,S)-1-(2,4-дихлорфенил)-4,4-диметил-2-(1Н-1,2,4-триазол-1-ил)пент-1-ен-3-ол (II.4);(Z)-2-(1Н-1,2,4-триазол-1-илметил)-2-(4-фторфенил)-3-(2-хлорфенил)оксиран (II.5);4-(4-хлорфенил)-2-фенил-2-(1Н-1,2,4-триазолметил)бутиронитрил (II.6);3-(2,4-дихлорфенил)-6-фтор-2-(1Н-1,2,4-триазол-1-ил)хиназолин-4(3Н)-он (II.7);бис(4-фторфенил)(метил)(1Н-1,2,4-триазол-1-илметил)силан (II.8);(R,S)-2-(2,4-дихлорфенил)-1-(1Н-1,2,4-триазол-1-ил)гексан-2-ол (II.9);(1RS,5RS;1RS,5SR)-5-(4-хлорбензил)-2,2-диметил-1-(1Н-1,2,4-триазол-1-илметил)цикпопентанол (II.10);N-пропил-N-[2-(2,4,6-трихлорфенокси)этил]имидазол-1-карбоксамид (II.11);(±)-1-[2-(2,4-дихлорфенил)-4-пропил-1,3-диоксолан-2-илметил]-1Н-1,2,4-триазол (II.12);(R,S)-1-(4-хлорфенил)-4,4-диметил-3-(1Н-1,2,4-триазол-1-илметил)пентан-3-ол (II.13);(±)-2-(2,4-дихлорфенил)-3-(1Н-1,2,4-триазолил)пропил-1,1,2,2-тетрафторэтиловыйэфир (II.14) и(Е)-1-[1-[[4-хлор-2-(трифтормтеил)фенил]имино]-2-пропоксиэтил]-1Н-имидазол (II.15);(R,S)-2,4'-дифтор-α-(1Н-1,2,4-триазол-1-илметил)бензгидриловыйспирт (II.16);2-п-хлорфенил-2-(1Н-1,2,4-триазол-1-илметил)гексаненитрил (II.17)всинергетическиэффективномколичестве.Крометого, описанспособборьбыс фитопатогеннымигрибами, характеризующийсятем, чтогрибы, ихпространствопроизрастанияилиподлежащиезащитеотпораженияимиматериалы, растения, почву, семена, поверхностиилипомещенияобрабатываютфунгициднойсмесьюпоодномуизпп.1-3, причемдействующиевещества, аименноамидноесоединениеформулы Iби азолформул II.1-II.17, применяютодновременно, аименносовместноилираздельно, илипоследовательно.

公开(公告)号：HU188325B

公开(公告)日：1986-04-28

申请号：HU247482

申请日：1982-07-30

Applicant: BASF AG

Inventor： EICKEN KARL ,  SCHEIB KLAUS ,  THEOBALD HANS ,  POMMER ERNST-HEINRICH ,  AMMERMAN EBERHARD

IPC: A01N43/90 ,  A01N45/02 ,  C07D487/04

Abstract: 7-Aminoazolo[1,5-a]pyrimidine of the formula where R1 is unsubstituted or substituted alkyl, halogen, alkoxy, cyano, or cycloalkyl, or is aryl, aryloxy, arylthio, arylalkyl, arylalkoxy or arylalkylthio, each of which may be substituted, or is indane, tetrahydronaphthalene or benzene, each of which may be substituted and is fused to the phenyl ring, R2 and R3 are each hydrogen, alkyl or aryl, n is 1 or 2, A is nitrogen or a CR4 group, where R4 has the meanings of R2 and may furthermore be halogen, cyano or alkoxycarbonyl, or together with R3 is alkylene which may have up to 2 double bonds, and fungicides containing these compounds.

公开(公告)号：IN835CH1997A

公开(公告)日：2005-03-04

申请号：IN835CH1997

申请日：1997-04-23

Applicant: BASF AG

Inventor： MUELLER BERND ,  SAUTER HUBERT ,  AMMERMAN EBERHARD ,  LORENZ GISELA ,  STRATHMANN SIEGFRIED ,  SAUR REINHOLD ,  SCHELBERGER KLAUS ,  LEYENDECKER JOACHIM

IPC: A01N20060101 ,  A01N37/50 ,  A01N37/52 ,  A01N47/24 ,  A01N47/38

Abstract: Synergistic fungicidal mixture comprises: (a) a carbamate of formula (I); and at least one compound selected from: (b) an oxime ether of formula (II); (c) an oxime ether carboxylic acid ester of formula (IIIa), oxime ether carboxylic acid amide of formula (IIIb), methoxyacrylic acid ester of formula (IIIc); (d) an azole derivative (IV) selected from 1-[(2RS,4RS;2RS,4SR)-4-bromo-2-(2,4-dichlorophenyl)tetrahydrofuryl]-1H-1,2,4-triazole (IVa); 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol (IVb); (+)/(-)-4-chloro-4-[4-methyl-2-(1H-1,2,4-triazol-1-ylmethyl)-1,3-dioxolan-2-yl]phenyl-4-chlorophenylether (IVc); (E)-(R,S)-1-(2,4- dichlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pent-1-en-3-ol(IVd); (Z)-2-(1H-1,2,4-triazol-1-ylmethyl)-2-(4-fluorophenyl)-3-(2-chlorophenyl)oxirane (IVe); 4-(4-chlorophenyl)-2-phenyl-2-(1H-1,2,4-triazolylmethyl)butyronitrile (IVf); 3-(2,4-dichlorophenyl)-6-fluoro-2-(1H-1,2,4-triazol-1-yl)quinazolin-4(3H)-one (IVg); bis(4-fluorophenyl)(methyl)(1H-1,2,4-triazol-1-ylmethyl)silane (IVh); (R,S)-2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)hexan-2-ol (IVi); (1RS,5RS;1RS,5SR)-5-(4-chlorobenzyl)-2,2-dimethyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol (IVj); N-propyl-N-[2-(2,4,6-trichlorophenoxy)ethyl]imidazol-1-carboxamide (IVk); (+)/(-)-1-[2-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolan-2-ylmethyl]-1H-1,2,4-triazole (IVl); (R,S)-1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol (IVm); (+)/(-)-2-(2,4-dichlorophenyl)-3-(1H-1,2,4-triazol-1-yl)propyl-1,1,2,2-tetrafluoroethyl ether (IVn); (E)-1-[1[[4-chloro-2-(trifluoromethyl)phenyl]imino]-2-propoxyethyl]-1H-imidazole (IVo); (RS)-2,4'-difluoro-~a-(1H-1,2,4-triazol-1-ylmethyl)benzhydryl alcohol (IVp); 2-p-chlorophenyl-2-(1H-1,2,4-triazol-1-ylmethyl)hexane nitrile (IVq). T = CH or N; n = 0-2; R = halo, 1-4C alkyl or 1-4C haloalkyl; X = O or NH; Y = CH or N; Z = O, S, NH or 1-4C alkylamino; R' = 1-6C alkyl, 1-6C haloalkyl, 3-6C alkenyl, 2-6C haloalkenyl, 3-6C alkynyl, 3-6C haloalkynyl, (3-6C cycloalkyl)methyl or benzyl (optionally substituted by halo and/or 1-3 CN, 1-4C alkyl, 1-4C haloalkyl, 1-4C alkoxy, 1-4C haloalkoxy or 1-4C alkylthio).

公开(公告)号：NZ325256A

公开(公告)日：1999-11-29

申请号：NZ32525696

申请日：1996-12-16

Applicant: BASF AG

Inventor： GROTE THOMAS ,  SAUTER HUBERT ,  KIRSTGEN REINHARD ,  BAYER HERBERT ,  MULLER RUTH ,  MULLER BERND ,  OBERDORF KLAUS ,  GRAMMENOS WASSILIOS ,  GOTZ NORBERT ,  RACK MICHAEL ,  HARREUS ALBRECHT ,  ROHL FRANZ ,  AMMERMAN EBERHARD ,  HARRIES VOLKER ,  LORENZ GISELA ,  STRATHMANN SIEGFRIED

IPC: C07C249/04 ,  A01N37/50 ,  A01N43/40 ,  A01P3/00 ,  A01P7/00 ,  C07C251/50 ,  C07C251/56 ,  C07C251/58 ,  C07C251/60 ,  C07C255/40

Abstract: The present relates to 2-iminooxyphenylacetic acid derivatives of the formula 1 where the substitutents are defined in the specification, and method of treating fungi and animal pests, and process for the preparation of the compound.

公开(公告)号：ZA9703476B

公开(公告)日：1998-10-23

申请号：ZA9703476

申请日：1997-04-23

Applicant: BASF AG

Inventor： MUELLER BERND ,  SAUTER HUBERT ,  AMMERMAN EBERHARD ,  LORENZ GISELA ,  STRATHMANN SIEGFRIED ,  SAUR REINHOLD ,  SCHELBERGER KLAUS ,  LEYENDECKER JOACHIM

IPC: A01N20060101 ,  A01N47/24 ,  A01N

公开(公告)号：IN213019B

公开(公告)日：2008-03-28

申请号：IN835CH1997

申请日：1997-04-23

Applicant: BASF AG

Inventor： MUELLER BERND ,  SAUTER HUBERT ,  AMMERMAN EBERHARD ,  LORENZ GISELA ,  STRATHMANN SIEGFRIED ,  SAUR REINHOLD ,  SCHELBERGER KLAUS ,  LEYENDECKER JOACHIM

IPC: A01N20060101 ,  A01N37/50 ,  A01N37/52 ,  A01N47/24 ,  A01N47/38

Abstract: Synergistic fungicidal mixture comprises: (a) a carbamate of formula (I); and at least one compound selected from: (b) an oxime ether of formula (II); (c) an oxime ether carboxylic acid ester of formula (IIIa), oxime ether carboxylic acid amide of formula (IIIb), methoxyacrylic acid ester of formula (IIIc); (d) an azole derivative (IV) selected from 1-[(2RS,4RS;2RS,4SR)-4-bromo-2-(2,4-dichlorophenyl)tetrahydrofuryl]-1H-1,2,4-triazole (IVa); 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol (IVb); (+)/(-)-4-chloro-4-[4-methyl-2-(1H-1,2,4-triazol-1-ylmethyl)-1,3-dioxolan-2-yl]phenyl-4-chlorophenylether (IVc); (E)-(R,S)-1-(2,4- dichlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pent-1-en-3-ol(IVd); (Z)-2-(1H-1,2,4-triazol-1-ylmethyl)-2-(4-fluorophenyl)-3-(2-chlorophenyl)oxirane (IVe); 4-(4-chlorophenyl)-2-phenyl-2-(1H-1,2,4-triazolylmethyl)butyronitrile (IVf); 3-(2,4-dichlorophenyl)-6-fluoro-2-(1H-1,2,4-triazol-1-yl)quinazolin-4(3H)-one (IVg); bis(4-fluorophenyl)(methyl)(1H-1,2,4-triazol-1-ylmethyl)silane (IVh); (R,S)-2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)hexan-2-ol (IVi); (1RS,5RS;1RS,5SR)-5-(4-chlorobenzyl)-2,2-dimethyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol (IVj); N-propyl-N-[2-(2,4,6-trichlorophenoxy)ethyl]imidazol-1-carboxamide (IVk); (+)/(-)-1-[2-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolan-2-ylmethyl]-1H-1,2,4-triazole (IVl); (R,S)-1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol (IVm); (+)/(-)-2-(2,4-dichlorophenyl)-3-(1H-1,2,4-triazol-1-yl)propyl-1,1,2,2-tetrafluoroethyl ether (IVn); (E)-1-[1[[4-chloro-2-(trifluoromethyl)phenyl]imino]-2-propoxyethyl]-1H-imidazole (IVo); (RS)-2,4'-difluoro-~a-(1H-1,2,4-triazol-1-ylmethyl)benzhydryl alcohol (IVp); 2-p-chlorophenyl-2-(1H-1,2,4-triazol-1-ylmethyl)hexane nitrile (IVq). T = CH or N; n = 0-2; R = halo, 1-4C alkyl or 1-4C haloalkyl; X = O or NH; Y = CH or N; Z = O, S, NH or 1-4C alkylamino; R' = 1-6C alkyl, 1-6C haloalkyl, 3-6C alkenyl, 2-6C haloalkenyl, 3-6C alkynyl, 3-6C haloalkynyl, (3-6C cycloalkyl)methyl or benzyl (optionally substituted by halo and/or 1-3 CN, 1-4C alkyl, 1-4C haloalkyl, 1-4C alkoxy, 1-4C haloalkoxy or 1-4C alkylthio).