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    1,3-oxazoline and 1,3-thiazoline derivatives, their preparation, and their use as pesticides
    12.
    发明授权
    1,3-oxazoline and 1,3-thiazoline derivatives, their preparation, and their use as pesticides 失效
    1,3-恶唑啉和1,3-噻唑啉衍生物，它们的制备及其作为农药的用途

    公开(公告)号：US06265350B1

    公开(公告)日：2001-07-24

    申请号：US09332225

    申请日：1999-06-14

    申请人： Stefan Schnatterer ,  Manfred Kern ,  Ulrich Sanft

    发明人： Stefan Schnatterer ,  Manfred Kern ,  Ulrich Sanft

    IPC分类号： A01N4340

    CPC分类号： C07D413/10 ,  A01N43/74 ,  C07D413/14 ,  C07D417/10

    摘要： 1,3-Oxazoline and 1,3-thiazoline derivatives, their preparation, and their use as pesticides 1,3-Oxazoline and 1,3-thiazoline derivatives of the formula (I) where the symbols have the following meanings: A is phenyl, pyridyl, pyrimidinyl, pyrazinyl, pyrazolyl or thienyl, E is a single bond, (C1-C4)alkylene, —O—CH2— or —CH2—O—; G is a radical selected from the group consisting of Z is oxygen or sulfur. Compounds of the formula (I) have, in particular, a very good acaricidal and insecticidal action with regard to the spectrum of action and the potency.

    摘要翻译： 1,3-唑啉和1,3-噻唑啉衍生物，它们的制备及其作为农药的用途，1,3-恶唑啉和式（I）的1,3-噻唑啉衍生物，其中符号具有以下含义：A是苯基， 吡啶基，嘧啶基，吡嗪基，吡唑基或噻吩基，E是单键，（C1-C4）亚烷基，-O-CH2-或-CH2-O-; G是选自Z是氧或硫的基团。 式（I）化合物尤其具有关于作用光谱和效力的非常好的杀螨和杀虫作用。

    Method for producing N-sulfonyl-substituted oxindoles
    13.
    发明授权
    Method for producing N-sulfonyl-substituted oxindoles 有权
    N-磺酰基取代的羟基吲哚的制备方法

    公开(公告)号：US08969553B2

    公开(公告)日：2015-03-03

    申请号：US13995898

    申请日：2011-12-19

    申请人： Gunter Karig ,  Mark James Ford ,  Konrad Siegel ,  Stefan Schnatterer

    发明人： Gunter Karig ,  Mark James Ford ,  Konrad Siegel ,  Stefan Schnatterer

    IPC分类号： C07D403/04 ,  C07D251/20 ,  A01N43/38 ,  A01N43/66

    CPC分类号： C07D251/20 ,  A01N43/38 ,  A01N43/66 ,  C07D401/04 ,  C07D403/04

    摘要： Process for the selective N-sulfonylation of oxindoles, in particular process for the N-sulfonylation of 3-triazinyloxindoles, and also N-sulfonyl-substituted 3-triazinyloxindoles and the use of N-sulfonyl-substituted oxindoles and of N-sulfonyl-substituted 3-triazinyloxindoles as intermediates for the synthesis of fine chemicals and of active ingredients in the field of pharmacy and agriculture, and also the use of these compounds as active ingredients in the field of agriculture.

    摘要翻译： 用于N-羟基吲哚的选择性N-磺酰化的方法，特别是3-三嗪基氧基吲哚的N-磺酰化方法，以及N-磺酰基取代的3-三嗪并氧基吲哚和使用N-磺酰基取代的羟基吲哚和N-磺酰基取代的 3-三嗪基氧吲哚作为合成精细化学品和药物和农业领域的活性成分的中间体，以及这些化合物作为农业领域的活性成分的用途。

    HERBICIDE COMBINATION COMPRISING DIMETHOXYTRIAZINYL SUBSTITUTED DIFLUOROMETHANESULFONYLANILIDES
    16.
    发明申请
    HERBICIDE COMBINATION COMPRISING DIMETHOXYTRIAZINYL SUBSTITUTED DIFLUOROMETHANESULFONYLANILIDES 审中-公开
    包含二甲氧基硅烷取代的二氟甲磺酰胺的除草剂组合

    公开(公告)号：US20100069248A1

    公开(公告)日：2010-03-18

    申请号：US12541088

    申请日：2009-08-13

    申请人： Erwin Hacker ,  Christopher Hugh Rosinger ,  Christian Waldraff ,  Chieko Ueno ,  Georg Bonfig-Picard ,  Stefan Schnatterer ,  Shinichi Shirakura

    发明人： Erwin Hacker ,  Christopher Hugh Rosinger ,  Christian Waldraff ,  Chieko Ueno ,  Georg Bonfig-Picard ,  Stefan Schnatterer ,  Shinichi Shirakura

    IPC分类号： A01N43/66 ,  A01P13/00

    CPC分类号： A01N43/66 ,  A01N37/10 ,  A01N37/18 ,  A01N37/40 ,  A01N39/04 ,  A01N43/38 ,  A01N43/40 ,  A01N43/42 ,  A01N43/54 ,  A01N2300/00

    摘要： The present invention relates to a herbicide combination comprising components (A) and (B) where (A) denotes one or more compounds or salts thereof from the group described by the general formula (I): in which R1 is halogen, preferably fluorine or chlorine, R2 is hydrogen and R3 is hydroxyl or R2 and R3 together with the carbon atom to which they are attached are a carbonyl group C═O and R4 is hydrogen or methyl; and (B) denotes one or more herbicides from the group of the (het)arylcarboxylic acids consisting of: (B1-1) dicamba; (B1-2) 2,3,6-TBA; (B2-1) clopyralid; (B2-2) fluoroxypyr; (B2-3) inabenfide; (B2-4) picloram; (B2-5) triclopyr; (B3-1) quinclorac; (B3-2) quinmerac; (B4-1) indolyl-3-ylacetic acid; (B4-2) 4-indol-3-ylbutyric acid; (B5-1) 2-(1-naphthyl)acetamide; (B5-2) 1-naphthylacetic acid; (B5-3) 2-naphthyloxyacetic acid; (B5-4) aminocyclopyrachlor.

    摘要翻译： 本发明涉及包含组分（A）和（B）的除草剂组合，其中（A）表示一种或多种由通式（I）所示的基团的化合物或其盐：其中R 1是卤素，优选氟或 氯，R2是氢，R3是羟基或R2和R3与它们所连接的碳原子一起是羰基，C = O，R4是氢或甲基; 和（B）表示由以下组成的（het）芳基羧酸的一种或多种除草剂：（B1-1）麦草畏; （B1-2）2,3,6-TBA; （B2-1）氯吡啶; （B2-2）氟氧吡啶; （B2-3）不可靠; （B2-4）pic lor am （B2-5）triclopyr; （B3-1）喹草酸; （B3-2）quinmerac; （B4-1）吲哚基-3-基乙酸; （B4-2）4-吲哚-3-基丁酸; （B5-1）2-（1-萘基）乙酰胺; （B5-2）1-萘基乙酸; （B5-3）2-萘氧基乙酸; （B5-4）氨基环吡啶。