BENZYL AMIDOXIME DERIVATIVES, INTERMEDIATE PRODUCTS AND METHOD FOR THEIR PRODUCTION AND USE AS FUNGICIDES
    11.
    发明申请
    BENZYL AMIDOXIME DERIVATIVES, INTERMEDIATE PRODUCTS AND METHOD FOR THEIR PRODUCTION AND USE AS FUNGICIDES 审中-公开
    BENZYLAMIDOXIM衍生物,中间产品和工艺及其及其作为杀菌剂

    公开(公告)号:WO0125187A3

    公开(公告)日:2001-11-01

    申请号:PCT/EP0009744

    申请日:2000-10-05

    CPC classification number: C07C259/14 A01N37/52 C07C2601/02

    Abstract: The invention relates to benzyl amidoxime derivatives of formula (I) as fungicides wherein: A represents an aryl or heteraryl radical; Y represents a straight-chained or branched C1-C4 alkylene group, whereby a carbon atom can be substituted by an oxygen, nitrogen or sulphur atom or by a cyclopropyl group; Rn represents one to five similar or different radicals from the group consisting of hydrogen, halogen, C1-C6 alkyl, C1-C6 alkoxy, C1-C4 halogen alkyl, C1-C4 halogen alkoxy, C1-C4 alkylthio, C1-C4 alkoxyalkoxy; R represents optionally substituted phenyl C1-C6 alkyl, thienyl C1-C4 alkyl, or pyrazolyl C1-C4 alkyl, Rp represents one to five similar or different radicals from the group consisting of hydrogen, halogen, C1-C6 alkyl, C1-C6 alkoxy, C1-C4 halogen alkyl, C1-C4 halogen alkoxy, C1-C4 alkylthio, C1-C4 alkoxyalkoxy, C1-C6 alkyl carbonyl; n represents 0-5; and p represents 0-4, according to the number of free valences.

    Abstract translation: 本申请涉及式(I)作为杀真菌剂的Benzylamidoxim衍生物。 其中A为芳基或杂芳基; Y线性或支链的C1-C4亚烷基,其中一个碳原子可以被氧,氮或硫原子或由环丙基取代; RN <1>一至选自五个相同或不同的基团:氢,卤素,C1-C6烷基,C1-C6-烷氧基,C1-C4卤代烷基,C1-C4卤代烷氧基,C1-C4烷硫基,C1 -C4烷氧烷; [R <2>任选取代的苯基-C 1 -C 6 - 烷基,噻吩基-C 1 -C 4 - 烷基,或吡唑基-C 1 -C 4 - 烷基,卢比<3>一个从组五个相同或不同的基团:氢,卤素 ,C1-C6烷基,C1-C6-烷氧基,C1-C4卤代烷基,C1-C4卤代烷氧基,C1-C4烷硫基,C1-C4烷氧基烷氧基,C1-C6烷基羰基; n为0-5; p取决于自由价的0-4的数量。

    FUNGICIDAL MIXTURES
    14.
    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

    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
    15.
    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

    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。

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