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    FUNGICIDAL MIXTURES
    52.
    发明申请
    FUNGICIDAL MIXTURES 审中-公开
    杀菌剂混合工

    公开(公告)号：WO02056685A2

    公开(公告)日：2002-07-25

    申请号：PCT/EP0200412

    申请日：2002-01-17

    Applicant: BASF AG ,  GROTE THOMAS ,  ROSE INGO ,  AMMERMANN EBERHARD ,  STIERL REINHARD ,  LORENZ GISELA ,  STRATHMANN SIEGFRIED ,  SCHERER MARIA ,  SCHELBERGER KLAUS ,  HADEN EGON

    Inventor： GROTE THOMAS ,  ROSE INGO ,  AMMERMANN EBERHARD ,  STIERL REINHARD ,  LORENZ GISELA ,  STRATHMANN SIEGFRIED ,  SCHERER MARIA ,  SCHELBERGER KLAUS ,  HADEN EGON

    IPC: A01N25/04 ,  A01N35/04 ,  A01N35/10 ,  A01N37/50 ,  A01N35/00

    CPC classification number: A01N35/04 ,  A01N37/50 ,  A01N2300/00

    Abstract: The invention relates to fungicidal mixtures containing a) benzophenones of formula (I), where R = chloro, methyl, methoxy, acetoxy, pivaloyloxy or hydroxy; R = chloro or methyl; R = H, halogen or methyl and R = C1-C6 alkyl or benzyl, where the phenyl moiety of the benzyl group may be halo- or methyl-substituted and b) trisoximethers of formula (II), where X = NH or O; R , R , independently = C1-C4 alkyl or cyclopropyl; R , R , independently = C1-C4 alkyl, C3-C4 alkenyl or cyclopropyl; in synergistically effective amounts. The invention further relates to the treatment of noxious fungi with mixtures of compounds (I) and (II) and agents containing the same.

    Abstract translation: 含有式（I）中R <1>表示氯，甲基，甲氧基，乙酰氧基，新戊酰氧基或羟基的二苯甲酮类A9的杀真菌混合物; [R <2>是氯或甲基; [R <3>为氢，卤素或甲基; 且R <4>是氢，卤素或甲基; 并代表C1-C6烷基或苄基，其中基团，苄基的苯基部分可以带有卤素或甲基取代基，和b）式Trisoximether（II）其中取代基具有以下含义：X是NH或氧; [R <5>，R <7>独立地是C1-C4烷基或环丙基; [R <6>，R <8>独立地是C1-C4烷基，C3-C4链烯基或环丙基; 包含协同有效量的组合物，用于控制使用（I）和（II）的化合物的混合物和有害真菌的方法。

    USE OF SUBSTITUTED IMIDAZOAZINES, NOVEL IMIDAZOAZINES, METHODS FOR THE PRODUCTION THEREOF, AND AGENTS CONTAINING THESE COMPOUNDS
    53.
    发明申请
    USE OF SUBSTITUTED IMIDAZOAZINES, NOVEL IMIDAZOAZINES, METHODS FOR THE PRODUCTION THEREOF, AND AGENTS CONTAINING THESE COMPOUNDS 审中-公开
    USE取代IMIDAZOAZINEN，新imidazoazines，制造方法，和代理人含

    公开(公告)号：WO0248146A2

    公开(公告)日：2002-06-20

    申请号：PCT/EP0114577

    申请日：2001-12-12

    Applicant: BASF AG ,  CULLMANN OLIVER ,  GEWEHR MARKUS ,  GRAMMENOS WASSILIOS ,  TORMO I BLASCO JORDI ,  MUELLER BERND ,  SAUTER HUBERT ,  GYPSER ANDREAS ,  GROTE THOMAS ,  RHEINHEIMER JOACHIM ,  ROSE INGO ,  SCHIEWECK FRANK ,  AMMERMANN EBERHARD ,  STRATHMANN SIEGFRIED ,  LORENZ GISELA ,  STIERL REINHARD

    Inventor： CULLMANN OLIVER ,  GEWEHR MARKUS ,  GRAMMENOS WASSILIOS ,  TORMO I BLASCO JORDI ,  MUELLER BERND ,  SAUTER HUBERT ,  GYPSER ANDREAS ,  GROTE THOMAS ,  RHEINHEIMER JOACHIM ,  ROSE INGO ,  SCHIEWECK FRANK ,  AMMERMANN EBERHARD ,  STRATHMANN SIEGFRIED ,  LORENZ GISELA ,  STIERL REINHARD

    IPC: A01N43/90 ,  C07D471/04 ,  C07D487/04

    CPC classification number: C07D471/04 ,  A01N43/90 ,  C07D487/04

    Abstract: The invention relates to the use of substituted imidazoazines of formula (I), in which the variables have the following meanings: R represents alkyl, phenyl, phenylalkyl, naphthyl, anthracenyl, cycloalkyl, 5-membered or 6-membered hetaryl or 5-membered or 6-membered heterocyclyl, containing one to three N atoms and/or one O atom or S atom or one or two O atoms and/or S atoms, or condensed 8-membered to 12-membered hetaryl or condensed 8-membered to 12-membered heterocyclyl, containing one to four N atoms and/or one O atom or S atom or one or two O atoms and/or S atoms, whereby R can be unsubstituted or can be substituted as cited in the description; R and R represent hydrogen, alkyl, alkenyl, alkynyl, alkyl halide, alkenyl halide, alkynyl halide, trialkyl silylalkyl, phenyl, phenylalkyl or R and R , together with the bridging N atom, form a 5-membered or 6-membered heterocyclic or heteroaromatic ring, which can be interrupted by one to three N atoms and/or one O atom or S atom or by one or two O atoms and/or S atoms, and which can be substituted; A and B represent N or CR ; R , R and R represent hydrogen, halogen, cyano, nitro, hydroxy, alkyl, alkyl halide, cycloalkyl, alkoxy, alkoxy halide, alkylthio, amino, alkyl amino, dialkylamino, alkenyl, alkenyloxy, alkynyl or alkynyloxy. The inventive compounds are used for controlling phytopathogenic harmful fungi. The invention further relates to agents containing the inventive compounds, to novel imidazoazines, and to methods for the production thereof.

    Abstract translation: 使用式（I）的取代的Imidazoazinen的，其中各变量具有以下含义：R t <1>是烷基，苯基，苯基烷基，萘基，蒽基，环烷基，5-或6-员杂芳基或5-或6-元杂环基 含有1至3个N原子和/或一个O或S原子或一个或两个O和/或S原子，或稠合8-12 gliederiges杂芳基或稠合的8-12 gliederiges杂环基， 含有一至四个N原子和/或一个O或S原子或一个或两个O和/或O原子，其中R是未取代的<1>或作为可在本说明书中被取代; [R <2>，R <3>是氢，烷基，烯基，炔基，卤代烷基，卤代烯基，卤代炔基，三烷基甲硅烷基，苯基，苯基烷基或R <2>，R <3>连同桥接氮原子的5-或6- 形成 - 元杂环基或可被一至三个N原子和/或一个O或S原子或一个或两个O和/或S原子被中断杂芳族环; A，B，N或CR <4>; [R <4>，R <5> - [R <6>为氢，卤素，氰基，硝基，羟基，烷基，卤代烷基，环烷基，烷氧基，卤代烷氧基，烷硫基，氨基，烷基氨基，二烷基氨基，烯基，烯氧基，炔氧基或炔氧基; 防治植物病原性有害真菌的，含有它们，它们的制备新imidazoazines和方法的组合物。

    FUNGICIDE MIXTURES BASED ON PYRIDINE CARBOXAMIDES_
    57.
    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。

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