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    FUNGICIDE MIXTURES BASED ON PYRIDINE CARBOXAMIDES_
    61.
    发明申请
    FUNGICIDE MIXTURES BASED ON PYRIDINE CARBOXAMIDES_ 审中-公开
    基于吡啶甲酰胺杀菌剂混合工

    公开(公告)号：WO9931981A3

    公开(公告)日：1999-08-26

    申请号：PCT/EP9808231

    申请日：1998-12-15

    Applicant: BASF AG ,  SCHELBERGER KLAUS ,  SCHERER MARIA ,  EICKEN KARL ,  HAMPEL MANFRED ,  AMMERMANN EBERHARD ,  LORENZ GISELA ,  STRATHMANN SIEGFRIED

    Inventor： SCHELBERGER KLAUS ,  SCHERER MARIA ,  EICKEN KARL ,  HAMPEL MANFRED ,  AMMERMANN EBERHARD ,  LORENZ GISELA ,  STRATHMANN SIEGFRIED

    IPC: A01N37/32 ,  A01N43/00 ,  A01N43/38 ,  A01N43/40 ,  A01N43/54 ,  A01N43/76 ,  A01N47/04 ,  A01N47/38

    CPC classification number: A01N43/40 ,  A01N53/00 ,  A01N47/38 ,  A01N47/04 ,  A01N43/76 ,  A01N43/54 ,  A01N43/36 ,  A01N37/32 ,  A01N2300/00

    Abstract: The invention relates to fungicide mixtures containing, as active components, a) an amide compound of formula (I) A-CO-NR R , wherein A represents an aryl group or an aromatic or non-aromatic, 5- or 6-structured heterocyclic compound having 1 to 3 heteroatoms selected from O, N, S; whereby the aryl group or the heterocyclic compound can optionally comprise 1, 2 or 3 substituents selected independently of one another from alkyl, halogen, CHF2, CF3, alkoxyl, haloalkoxyl, alkylthio, alkyl sulfinyl and alkyl sulfonyl; R represents a hydrogen atom; R represents a phenyl group or cycloalkyl group optionally containing 1, 2 or 3 substituents selected independently of one another from alkyl, alkenyl, alkynyl, alkoxyl, alkenyloxyl, alkynyloxyl, cycloalkyl, cycloalkenyl, cycolalkyloxyl, cycloalkenyloxyl, phenyl and halogen, whereby the aliphatic and cycloaliphatic radicals can be partially or completely halogenated and/or the cycloaliphatic radicals can be substituted by 1 to 3 alkyl groups, whereby the phenyl group can contain 1 to 5 halogen atoms and/or 1 to 3 substituents selected independently of one another from alkyl, haloalkyl, alkoxyl, haloxyl, alkylthio and haloalkylthio, and whereby the amidic phenyl group is optionally condensed with a saturated 5-structured ring which is optionally substituted by one or more alkyl groups and/or can comprise a heteroatom selected from O and S, and b) fungicides from the group of dicarboximides, and/or c) pyrimidine derivatives of formula (III) in which R represents methyl, propyne-1-yl or cyclopropyl, and/or d) fludioxinil or fenpiclonil and/or captan, captafol or folpet, and/or f) fluazinam, and/or g) dichlofluanid or tolyl fluanid. The active components are provided in a synergistically effective quantity.

    Abstract translation: 一种杀真菌混合物，包含：a）式（I的酰胺化合物）作为活性组分A-CO-NR <1> [R <2>，其中A，芳基或芳族或非芳族5-或6-元杂环 具有选自O，N和S的1至3个杂原子; 其中芳基或杂环还可以如图1所示，可以具有从烷基，卤素，CHF 2，CF 3，烷氧基，卤代烷氧基，烷硫基，烷基亚磺酰基和烷基磺酰基独立地选自1,2或3个取代基; [R <1>是氢原子; [R <2>是任选具有选自烷基，烯基，炔基，烷氧基，烯氧基，炔氧基，环烷基，环烯基，环烷基氧基，环烯氧基，苯基独立选择的1，2或3个取代基的苯基或环烷基基团和 卤素，其中所述脂族和脂环族基团可以部分或完全被卤代和/或所述脂环族基团可以被1至3个烷基的基团取代，并且其中苯基可以具有独立地选自1至5个卤素原子和/或1至3个取代基 是烷基，卤代烷基，烷氧基，卤代烷氧基，烷硫基和卤代烷硫基，并且其中所述酰胺苯基被任选地稠合到饱和的5-元环，其任选地被一个或多个烷基和/或杂原子取代的选自O和S中的 可以具有，和b）选自迪杀真菌剂 甲酰亚胺，和/或c）使式III，其中R是甲基，丙炔-1-基或环丙基，和/或d）Fludioxinil或拌种咯和/或e）克菌丹，敌菌丹的嘧啶衍生物或其可灭菌丹和/或f）氟啶胺 和/或g）对甲抑菌灵抑菌灵或以协同有效量。

    FUNGICIDE MIXTURE
    69.
    发明专利
    FUNGICIDE MIXTURE 未知

    公开(公告)号：HU227961B1

    公开(公告)日：2012-07-30

    申请号：HU9903657

    申请日：1997-04-23

    Applicant: BASF AG

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

    IPC: A01N47/24 ,  A01N20060101 ,  A01N37/50 ,  A01N37/52 ,  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).

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