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    Selective herbicides based on a substituted phenylsulphonylaminocarbonyl-triazolinone
    2.
    发明授权
    Selective herbicides based on a substituted phenylsulphonylaminocarbonyl-triazolinone 失效
    基于取代的苯基磺酰基氨基羰基 - 三唑啉酮的选择性除草剂

    公开(公告)号：US07651978B2

    公开(公告)日：2010-01-26

    申请号：US10393359

    申请日：2003-03-21

    Applicant: Dieter Feucht ,  Hans-Joachim Santel ,  Klaus Lürssen ,  Ingo Wetcholowsky ,  Peter Dahmen ,  Klaus-Helmut Müller

    Inventor： Dieter Feucht ,  Hans-Joachim Santel ,  Klaus Lürssen ,  Ingo Wetcholowsky ,  Peter Dahmen ,  Klaus-Helmut Müller

    IPC: A01N47/28 ,  A01N47/38 ,  C07D405/00

    CPC classification number: A01N47/38

    Abstract: The present invention relates to selective-herbicidal compositions, characterized in that they contain an effective amount of the compound 2-(2-trifluoromethoxy-phenylsulphonylaminocarbonyl)-4-methyl-5-methoxy-2,4-dihydro-3H-1,2,4-triazol-3-one of the formula (I) and/or of salts of the compound of the formula (I), and to the use of these compositions for the selective control of weeds in crops of cereals, in particular crops of wheat, and to methods for the selective control of weeds in crops of cereals by applying the compositions together with surfactants and/or customary extenders.

    Abstract translation: 本发明涉及选择性除草组合物，其特征在于它们含有有效量的化合物2-（2-三氟甲氧基 - 苯基磺酰基氨基羰基）-4-甲基-5-甲氧基-2,4-二氢-3H-1,2 （I）的4-三唑-3-酮和/或式（I）化合物的盐，以及这些组合物用于选择性地控制谷物，特别是作物中的杂草的用途 的小麦，以及通过将组合物与表面活性剂和/或常规增量剂一起施用来选择性地控制谷物作物中的杂草的方法。

    Substituted benzoylpyrazoles as herbicides
    4.
    发明授权
    Substituted benzoylpyrazoles as herbicides 失效
    取代的苯甲酰基吡唑作为除草剂

    公开(公告)号：US06746989B1

    公开(公告)日：2004-06-08

    申请号：US09937631

    申请日：2001-09-26

    Applicant: Klaus-Helmut Müller ,  Stefan Lehr ,  Otto Schallner ,  Hans-Georg Schwarz ,  Heinz-Jürgen Wroblowsky ,  Mark Wilhelm Drewes ,  Dieter Feucht ,  Rolf Pontzen ,  Ingo Wetcholowsky

    Inventor： Klaus-Helmut Müller ,  Stefan Lehr ,  Otto Schallner ,  Hans-Georg Schwarz ,  Heinz-Jürgen Wroblowsky ,  Mark Wilhelm Drewes ,  Dieter Feucht ,  Rolf Pontzen ,  Ingo Wetcholowsky

    IPC: A01N43647

    CPC classification number: C07D401/10 ,  C07D403/10 ,  C07D413/10 ,  C07D417/10 ,  C07D471/04 ,  C07D487/04

    Abstract: The invention relates to novel substituted benzoylpyrazoles of the general formula (I), in which n represents the numbers 0, 1, 2 or 3, A represents a single bond or represents alkanediyl(alkylene), R1 represents in each case optionally substituted alkyl, alkenyl, alkinyl or cycloalkyl, R2 represents hydrogen, cyano, carbamoyl, thiocarbamoyl, halogen, or represents in each case optionally substituted alkyl, alkoxy, alkylthio, alkoxycarbonyl or cycloalkyl, R3 represents hydrogen, nitro, cyano, carboxyl, carbamoyl, thiocarbamoyl, halogen, or represents in each case optionally substituted alkyl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylamino, dialkylamino or dialkylaminosulfonyl, R4 represents nitro, cyano, carboxyl, carbamoyl, thiocarbamoyl, halogen, or represents in each case optionally substituted alkyl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylamino, dialkylamino or dialkylaminosulfonyl, Y represents hydrogen or represents in each case optionally substituted alkyl, alkylcarbonyl, alkoxycarbonyl, alkylsulfonyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkenyl, alkenylcarbonyl, alkenylsulfonyl, alkinyl, alkinylcarbonyl, cycloalkyl, cycloalkylcarbonyl, cycloalkylalkyl, phenylcarbonyl, phenylsulfonyl, phenylalkyl or phenylcarbonylalkyl, and Z represents an optionally substituted 4- to 12-membered saturated or unsaturated monocyclic or bicyclic heterocyclic grouping which contains 1 to 4 heteroatoms (up to 4 nitrogen atoms and optionally—alternatively or additionally—one oxygen atom or one sulfur atom, or an SO grouping or an SO2 grouping) and which additionally contains one to three oxo groups (C═O) and/or thioxo groups (C═S) as component of the heterocycle, and also to processes for their preparation and to their use as herbicides.

    Abstract translation: 本发明涉及通式（I）的新的取代的苯甲酰基吡唑，其中n代表数字0,1,2或3，A表示单键或表示烷二基（亚烷基），R 1表示在每种情况下任选取代 烷基，烯基，炔基或环烷基，R 2表示氢，氰基，氨基甲酰基，硫代氨基甲酰基，卤素，或在每种情况下表示任选取代的烷基，烷氧基，烷硫基，烷氧基羰基或环烷基，R 3表示氢，硝基，氰基 ，羧基，氨基甲酰基，硫代氨基甲酰基，卤素，或在每种情况下表示任选取代的烷基，烷氧基，烷硫基，烷基亚磺酰基，烷基磺酰基，烷基氨基，二烷基氨基或二烷基氨基磺酰基，R 4表示硝基，氰基，羧基，氨基甲酰基，硫代氨基甲酰基，卤素或 在每种情况下表示任选取代的烷基，烷氧基，烷硫基，烷基亚磺酰基，烷基磺酰基，烷基氨基，二烷基氨基或二烷基氨基磺酰基，Y表示氢或表示在任何情况下任选取代 烷基，烷基羰基，烷氧基羰基，烷基磺酰基，烷基氨基羰基，二烷基氨基羰基，烯基，烯基羰基，烯基磺酰基，炔基，烯基羰基，环烷基，环烷基羰基，环烷基烷基，苯基羰基，苯基磺酰基，苯基烷基或苯基羰基烷基，Z表示任选取代的4至12元饱和或不饱和 含有1至4个杂原子（最多4个氮原子，以及任选地或另外一个氧原子或一个硫原子，或一个SO基团或一个SO 2基团）的单环或双环杂环基团，并且另外含有一至三个氧代基 （C = O）和/或硫代基（C = S）作为杂环的组分，以及其制备方法及其作为除草剂的用途。

    Substituted thiazol(in) ylideneamino sulfonylamino (thio)carbonyl-triazolinones
    7.
    发明授权
    Substituted thiazol(in) ylideneamino sulfonylamino (thio)carbonyl-triazolinones 失效
    取代的噻唑（亚）氨基磺酰基氨基（硫代）羰基 - 三唑啉酮

    公开(公告)号：US06403535B1

    公开(公告)日：2002-06-11

    申请号：US09787479

    申请日：2001-04-27

    Applicant: Klaus-Helmut Müller ,  Klaus König ,  Johannes Rudolf Jansen ,  Ernst Rudolf F. Gesing ,  Mark Wilhelm Drewes ,  Markus Dollinger ,  Ingo Wetcholowsky

    Inventor： Klaus-Helmut Müller ,  Klaus König ,  Johannes Rudolf Jansen ,  Ernst Rudolf F. Gesing ,  Mark Wilhelm Drewes ,  Markus Dollinger ,  Ingo Wetcholowsky

    IPC: A01N4738

    CPC classification number: C07D417/12 ,  A01N47/38

    Abstract: The invention relates to novel substituted thiazol(in)ylidenaminosulphonyl-amino(thio)carbonyl-triazolinones of the formula (I) in which Q represents oxygen or sulphur, R1 represents hydrogen, amino, alkylideneamino or represents an in each case optionally substituted radical from the group consisting of alkyl, alkoxy, alkylamino, dialkylamino, alkanoylamino, alkenyl, alkinyl, alkenyloxy, cycloalkyl, cycloalkylalkyl, cycloalkylamino, aryl and arylalkyl, R2 represents hydrogen, cyano, halogen or represents an in each case optionally substituted radical from the group consisting of alkyl, alkoxy, alkylthio, alkylsulphinyl, alkylsulphonyl, alkylamino, dialkylamino, alkenyl, alkinyl, alkenyloxy, alkenylthio, alkenylamino, cycloalkyl, cycloalkylalkyl, cycloalkyloxy, cycloalkylthio, cycloalkylamino, aryl, aryloxy, arylthio, arylamino, arylalkyl, arylalkoxy, arylalkylthio and arylalkylamino, R3 represents an in each case optionally substituted radical from the group consisting of alkyl, alkoxy, alkenyl, alkinyl, cycloalkyl, cycloalkylalkyl, aryl and arylalkyl, R4 represents hydrogen, cyano, halogen or optionally substituted alkyl, R5 represents hydrogen, cyano, halogen or optionally substituted alkyl, and to salts of compounds of the formula (I), to processes for preparing the novel compounds and to their use as herbicides.

    Abstract translation: 本发明涉及式（I）中的新的取代的噻唑（亚氨基）磺酰基 - 氨基（硫代）羰基 - 三唑啉酮，其中Q表示氧或硫，R 1表示氢，氨基，亚烷基氨基或代表任意取代的基团， 由烷基，烷氧基，烷基氨基，二烷基氨基，烷酰基氨基，烯基，炔基，烯基氧基，环烷基，环烷基烷基，环烷基氨基，芳基和芳基烷基组成的基团，R 2表示氢，氰基，卤素或表示任意取代的基团， 烷基磺酰基，烷硫基，烷基亚磺酰基，烷基磺酰基，烷基氨基，二烷基氨基，烯基，炔基，烯基氧基，烯基硫基，烯基氨基，环烷基，环烷基烷基，环烷氧基，环烷基硫基，环烷基氨基，芳基，芳氧基，芳硫基，芳基氨基，芳基烷基，芳基烷氧基，芳基烷硫基和芳烷基氨基， R 3表示在每种情况下任选取代的基团，其由烷基，烷氧基， 烯基，环烷基，环烷基烷基，芳基和芳烷基，R 4表示氢，氰基，卤素或任选取代的烷基，R 5表示氢，氰基，卤素或任选取代的烷基，以及式（I）化合物的盐， 用于制备新化合物及其作为除草剂的用途。

    TERNARY FUNGICIDAL COMPOSITIONS COMPRISING A DITHIINO-TETRACARBOXAMIDE FUNGICIDE
    9.
    发明申请
    TERNARY FUNGICIDAL COMPOSITIONS COMPRISING A DITHIINO-TETRACARBOXAMIDE FUNGICIDE 审中-公开
    含有DITHIOO-TETRACARBOXAMIDE FUNGIC的第三方杀真菌剂组合物

    公开(公告)号：US20140121101A1

    公开(公告)日：2014-05-01

    申请号：US14110586

    申请日：2012-03-28

    Applicant: Ulrike Wachendorff-Neumann ,  Ingo Wetcholowsky ,  Anton Kraus ,  Thomas Seitz ,  Jose Augusto Geraldes

    Inventor： Ulrike Wachendorff-Neumann ,  Ingo Wetcholowsky ,  Anton Kraus ,  Thomas Seitz ,  Jose Augusto Geraldes

    IPC: A01N43/90 ,  A01N37/50 ,  A01N43/82

    CPC classification number: A01N43/90 ,  A01N37/50 ,  A01N43/653 ,  A01N43/82 ,  A01N61/00 ,  A01N2300/00

    Abstract: The present invention relates to active compound combinations, in particular within a fungicide composition, which comprises (A) a dithiino-tetracarboximide of formula (I), (B) an inhibitor of the ergosterol biosynthesis, in particular an azole compound, and (C) an inhibitor of the respiratory chain at complex III, in particular a strobilurin compound. Moreover, the invention relates to a method for curatively or preventively controlling the phytopathogenic fungi of plants or crops, to the use of a combination according to the invention for the treatment of seed, to a method for protecting a seed and not at least to the treated seed.

    Abstract translation: 本发明涉及特别是杀真菌剂组合物中的活性化合物组合物，其包含（A）式（I）的二硫代 - 四羧酰亚胺，（B）麦角固醇生物合成抑制剂，特别是唑类化合物和（C ）复合物III中呼吸链的抑制剂，特别是嗜球果伞素化合物。 此外，本发明涉及一种用于将植物或作物的植物病原性真菌或根据本发明的组合用于种子处理的方法或预防性控制方法，用于保护种子的方法，而不是至少 处理的种子。

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