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    Fungicide mixtures
    42.
    发明授权
    Fungicide mixtures 失效
    杀菌剂混合物

    公开(公告)号：US06211236B1

    公开(公告)日：2001-04-03

    申请号：US09171619

    申请日：1998-10-22

    申请人： Ruth Müller ,  Herbert Bayer ,  Hubert Sauter ,  Eberhard Ammermann ,  Gisela Lorenz ,  Siegfried Strathmann ,  Klaus Schelberger ,  Reinhold Saur

    发明人： Ruth Müller ,  Herbert Bayer ,  Hubert Sauter ,  Eberhard Ammermann ,  Gisela Lorenz ,  Siegfried Strathmann ,  Klaus Schelberger ,  Reinhold Saur

    IPC分类号： A01N3712

    CPC分类号： A01N37/52 ,  A01N55/00 ,  A01N47/38 ,  A01N43/653 ,  A01N43/54 ,  A01N37/50 ,  A01N2300/00

    摘要： A fungicidal mixture comprising a) an oxime ether of the formula I where the substituents have the following meanings: X is oxygen or amino (NH); Y is CH or N; Z is oxygen, sulfur, amino (NH) or C1-C4-alkylamino (N-alkyl); R′ is alkyl, haloalkyl, alkenyl, haloalkenyl, alkynyl, haloalkynyl, cycloalkylmethyl, or, if desired, substituted benzyl; a) an oxime ether of the formula I where the substituents have the following meanings: X is oxygen or amino (NH); Y is CH or N; Z is oxygen, sulfur, amino (NH) or C1-C4-alkylamino (N—C1-C4-alkyl); R′ is C1-C6-alkyl, C1-C6-haloalkyl, C3-C6-alkenyl, C2-C6-haloalkenyl, C3-C6-alkynyl, C3-C6-haloalkynyl, C3-C6-cycloalkylmethyl, or is benzyl which can be partially or fully halogenated and/or can have attached to it one to three of the following radicals: cyano, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-haloalkoxy and C1-C4-alkylthio; and at least one compound from groups b)-c): b.1) the oxime ether carboxylate of the formula IIa, b.2) the oxime ether carboxamide of the formula IIb, b.3) the methoxyacrylate of the formula IIc, c) one or more azole derivatives in a synergistically active amount.

    摘要翻译： 一种杀真菌混合物，其包含a）式I的肟醚，其中取代基具有以下含义：X是氧或氨基（NH）; Y是CH或N; Z是氧，硫，氨基（NH）或C 1 -C 4 - 烷基氨基 （N-烷基）; R'是烷基，卤代烷基，烯基，卤代烯基，炔基，卤代炔基，环烷基甲基，或如果需要，取代的苄基; a）式I的肟醚，其中取代基具有以下含义：X是氧 或氨基（NH）; Y是CH或N; Z是氧，硫，氨基（NH）或C 1 -C 4 - 烷基氨基（N-C 1 -C 4 - 烷基）; R'是C 1 -C 6烷基， - 卤代烷基，C 3 -C 6 - 烯基，C 2 -C 6 - 卤代烯基，C 3 -C 6 - 炔基，C 3 -C 6 - 卤代炔基，C 3 -C 6环烷基甲基，或者是可部分或完全卤化和/ 氰基，C 1 -C 4 - 烷基，C 1 -C 4卤代烷基，C 1 -C 4 - 烷氧基，C 1 -C 4 - 卤代烷氧基和C 1 -C 4 - 烷硫基中的一至三个基团;和至少一种基团b） -c）：b.1）式IIa的肟醚羧酸酯，b.2）肟醚羧酸酯 de的式IIb，b.3）式IIc的甲氧基丙烯酸酯，c）一种或多种协同活性量的唑衍生物。

    Fungicidal mixtures
    43.
    发明授权
    Fungicidal mixtures 失效

    公开(公告)号：US5994382A

    公开(公告)日：1999-11-30

    申请号：US983253

    申请日：1998-01-20

    申请人： Barbara Schwalge ,  Ruth Muller ,  Herbert Bayer ,  Hubert Sauter ,  Reinhold Saur ,  Klaus Schelberger ,  Eberhard Ammermann ,  Gisela Lorenz ,  Siegfried Strathmann

    发明人： Barbara Schwalge ,  Ruth Muller ,  Herbert Bayer ,  Hubert Sauter ,  Reinhold Saur ,  Klaus Schelberger ,  Eberhard Ammermann ,  Gisela Lorenz ,  Siegfried Strathmann

    IPC分类号： A01N37/50 ,  A01N43/647 ,  A01N55/10 ,  A01N37/18 ,  A01N43/50 ,  A01N43/54 ,  A01N55/00

    CPC分类号： A01N37/50

    摘要： Fungicidal mixture, comprisinga) an oxime ether carboxamide of the formula I ##STR1## where R is hydrogen or halogen and b) an azole derivative II selected from the group of the compounds II.1 to II.171-[(2RS,4RS;2RS,4SR)-4-bromo-2-(2,4-dichlorophenyl)-tetrahydrofuryl]-1H-1,2,4-triazole (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-yl-methyl)-1,3-dioxolan-2-yl]phenyl 4-chlorophenyl ether (II.3)(E)-(R,S)-1-(2,4-dichlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pent-1-en-3-ol (II.4)(Z)-2-(1H-1,2,4-triazol-1-ylmethyl)-2-(4-fluorophenyl)-3-(2-chlorophenyl)oxirane (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-yl-methyl)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-dimenthyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol [sic] (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) and(E)-1-[1-[[4-chloro-2-(trifluoromethyl)phenyl]imino]-2-propoxyethyl]-1H-imidazole (II.15)(RS)-2,4'-difluoro-.alpha.-(1H-1,2,4-triazol-1-ylmethyl)-benzhydryl alcohol (II.16)2-p-chlorophenyl-2-(1H-1,2,4-triazol-1-ylmethyl)-hexanenitrile (II.17)in a synergistically active amount.

    Fungicide mixtures
    45.
    发明授权
    Fungicide mixtures 失效
    杀菌剂混合物

    公开(公告)号：US6083946A

    公开(公告)日：2000-07-04

    申请号：US171601

    申请日：1998-10-22

    申请人： Bernd Muller ,  Hubert Sauter ,  Eberhard Ammermann ,  Gisela Lorenz ,  Siegfried Strathmann ,  Klaus Schelberger ,  Maria Scherer ,  Dietrich Mappes ,  Herbert Bayer ,  Ruth Muller

    发明人： Bernd Muller ,  Hubert Sauter ,  Eberhard Ammermann ,  Gisela Lorenz ,  Siegfried Strathmann ,  Klaus Schelberger ,  Maria Scherer ,  Dietrich Mappes ,  Herbert Bayer ,  Ruth Muller

    IPC分类号： A01N37/52 ,  A01N47/24 ,  A01N32/18 ,  A01N43/54 ,  A01N43/56 ,  A01N43/58 ,  A01N43/64

    CPC分类号： A01N37/52 ,  A01N47/24

    摘要： Fungicidal mixtures, comprisinga) a carbamate of the formula I ##STR1## where T is CH or N, n is 0, 1 or 2 and R is halogen, C.sub.1 -C.sub.4 -alkyl or C.sub.1 -C.sub.4 -haloalkyl, it being possible for the radicals R to be different when n is 2, and/orb) an oxime ether of the formula II ##STR2## where the substituents have the following meaning: X is oxygen or amino (NH);Y is CH or N;Z is oxygen, sulfur, amino (NH) or C.sub.1 -C.sub.4 -alkylamino (N--C.sub.1 -C.sub.4 -alkyl);R' is C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.3 -C.sub.6 -alkenyl, C.sub.2 -C.sub.6 -haloalkenyl, C.sub.3 -C.sub.6 -alkynyl, C.sub.3 -C.sub.6 -haloalkynyl, C.sub.3 -C.sub.6 -cycloalkylmethyl, or is benzyl which can be partially or fully halogenated and/or have attached to it one to three of the following radicals: cyano, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -haloalkyl, C.sub.1 -C.sub.4 -alkoxy, C.sub.1 -C.sub.4 -haloalkoxy, and C.sub.1 -C.sub.4 -alkylthio; andc) an acaricide selected from the group of the compounds III.a to III.d ##STR3## in a synergistically active amount.

    摘要翻译： PCT No.PCT / EP97 / 02044 Sec。 371日期：1998年10月22日 102（e）日期1998年10月22日PCT 1997年4月23日PCT公布。 公开号WO97 / 40676 日期1997年11月6日杀真菌混合物，其包含a）式I的氨基甲酸酯，其中T是CH或N，n是0,1或2，R是卤素，C 1 -C 4烷基或C 1 -C 4卤代烷基， 当n为2时，基团R可能不同，和/或b）式II的肟醚，其中取代基具有以下含义：X为氧或氨基（NH）; Y是CH或N; Z是氧，硫，氨基（NH）或C 1 -C 4烷基氨基（N-C 1 -C 4 - 烷基）; R'是C 1 -C 6 - 烷基，C 1 -C 6卤代烷基，C 3 -C 6 - 烯基，C 2 -C 6 - 卤代烯基，C 3 -C 6炔基，C 3 -C 6 - 卤代炔基，C 3 -C 6环烷基甲基， 被部分或完全卤化和/或连接到其一至三个以下基团：氰基，C 1 -C 4烷基，C 1 -C 4卤代烷基，C 1 -C 4 - 烷氧基，C 1 -C 4卤代烷氧基和C 1 -C 4 - 烷硫基; 和c）以协同活性量选自化合物III.a至III.d的杀螨剂。

    Fungicide mixtures
    46.
    发明授权
    Fungicide mixtures 失效
    杀菌剂混合物

    公开(公告)号：US6114378A

    公开(公告)日：2000-09-05

    申请号：US171522

    申请日：1998-10-21

    申请人： Ruth Muller ,  Herbert Bayer ,  Hubert Sauter ,  Eberhard Ammermann ,  Gisela Lorenz ,  Siegfried Strathmann ,  Klaus Schelberger ,  Maria Scherer

    发明人： Ruth Muller ,  Herbert Bayer ,  Hubert Sauter ,  Eberhard Ammermann ,  Gisela Lorenz ,  Siegfried Strathmann ,  Klaus Schelberger ,  Maria Scherer

    IPC分类号： A01N37/52 ,  A01N47/14 ,  A01N47/34 ,  A01N47/10 ,  A01N37/12 ,  A01N37/34 ,  A01N37/44

    CPC分类号： A01N37/52

    摘要： A fungicidal mixture comprisinga) an oxime ether of the formula I ##STR1## where the substituents have the following meaning: X is oxygen or amino (NH);Y is CH or N;Z is oxygen, sulfur, amino (NH) or C.sub.1 -C.sub.4 -alkylamino (N--C.sub.1 -C.sub.4 -alkyl);R' is C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.3 -C.sub.6 -alkenyl, C.sub.2 -C.sub.6 -haloalkenyl, C.sub.3 -C.sub.6 -alkynyl, C.sub.3 -C.sub.6 -haloalkynyl, C.sub.3 -C.sub.6 -cycloalkylmethyl, or benzyl which may be partially or fully halogenated and/or may carry one to three of the following radicals: cyano, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -haloalkyl, C.sub.1 -C.sub.4 -alkoxy, C.sub.1 -C.sub.4 -haloalkoxy and C.sub.1 -C.sub.4 -alkylthio;andb) a dithiocarbamate (II) selected from the group consisting ofmanganese ethylenebis(dithiocarbamate) (zinc complex) (IIa),manganese ethylenebis(dithiocarbamate) (IIb),zinc ammoniate ethylenebis(dithiocarbamate) (IIc) andzinc ethylenebis(dithiocarbamate) (IId) and/orc) 1-(2-cyano-2-methoxyiminoacetyl)-3-ethylurea (III)H.sub.3 CCH.sub.2 --NHCONH--C(CN).dbd.NOCH.sub.3 (III)in a synergistically active amount.

    摘要翻译： PCT No.PCT / EP97 / 02046 Sec。 371日期：1998年10月21日 102（e）1998年10月21日PCT PCT 1997年4月23日PCT公布。 公开号WO97 / 40677 日期1997年11月6日一种杀真菌混合物，其包含a）式I的肟醚，其中取代基具有以下含义：X是氧或氨基（NH）; Y是CH或N; Z是氧，硫，氨基（NH）或C 1 -C 4烷基氨基（N-C 1 -C 4 - 烷基）; R'是可以是C 1 -C 6 - 烷基，C 1 -C 6 - 卤代烷基，C 3 -C 6 - 烯基，C 2 -C 6 - 卤代烯基，C 3 -C 6 - 炔基，C 3 -C 6 - 卤代炔基，C 3 -C 6环烷基甲基或苄基 部分或完全卤化和/或可以携带一至三个以下基团：氰基，C 1 -C 4 - 烷基，C 1 -C 4卤代烷基，C 1 -C 4 - 烷氧基，C 1 -C 4 - 卤代烷氧基和C 1 -C 4烷硫基; （IIa），亚乙基双（二硫代氨基甲酸）亚乙酯（IIb），亚氨基亚氨基二（二硫代氨基甲酸）亚胺化锌（IIc））和亚乙基双（二硫代氨基甲酸锌）亚乙基双（二亚硫代氨基甲酸酯） ）（IId）和/或c）具有协同活性量的1-（2-氰基-2-甲氧基亚氨基乙酰基）-3-乙基脲（III）H3CCH2-NHCONH-C（CN）= NOCH3（III）

    Fungicidal mixtures
    47.
    发明授权
    Fungicidal mixtures 失效

    公开(公告)号：US5587365A

    公开(公告)日：1996-12-24

    申请号：US600822

    申请日：1996-02-13

    申请人： Horst Wingert ,  Hubert Sauter ,  Eberhard Ammermann ,  Gisela Lorenz ,  Reinhold Saur ,  Klaus Schelberger ,  Manfred Hampel

    发明人： Horst Wingert ,  Hubert Sauter ,  Eberhard Ammermann ,  Gisela Lorenz ,  Reinhold Saur ,  Klaus Schelberger ,  Manfred Hampel

    IPC分类号： A01N37/50 ,  A01N43/653 ,  A01N47/38 ,  A01N55/00 ,  A01N55/10 ,  A01N37/18 ,  A01N43/50 ,  A01N43/64

    CPC分类号： A01N37/50

    摘要： A fungicidal mixture containinga) the oxime ether carboxamide of the formula I ##STR1## and b) an azole derivative II selected from the group of compounds II.1 to II.161-[(2RS,4RS;2RS,4SR)-4-bromo-2-(2,4-dichlorophenyl)tetrahydrofuryl]-1H-1,2,4-triazole (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-yl-methyl)-1,3-dioxolan-2-yl]phenyl 4-chlorophenyl ether (II.3)(E)-(R,S)-1-(2,4-dichlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pent-1-en-3-ol (II.4)(Z)-2-(1H-1,2,4-triazol-1-ylmethyl)-2-(4-fluorophenyl)-3-(2-chlorophenyl)oxirane (II.5)4-(4-chlorophenyl)-2-phenyl-2-(1H-1,2,4-triazolyl methyl)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-yl-methyl)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-triazol-1-yl) 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-yl-methyl)benzhydryl alcohol (II.16)in a synergistically active amount is described.