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1. 发明授权

US06680402B2 Benzamidoxime derivatives, intermediates and processes for their preparation, and their use as fungicides 失效
标题翻译：苯甲酰胺肟衍生物，中间体及其制备方法及其作为杀真菌剂的用途
公开(公告)号：US06680402B2
公开(公告)日：2004-01-20
申请号：US10261122
申请日：2002-10-01
申请人： Karl Eicken , Joachim Rheinheimer , Frank Wetterich , Eberhard Ammermann , Gisela Lorenz , Siegfried Strathmann
发明人： Karl Eicken , Joachim Rheinheimer , Frank Wetterich , Eberhard Ammermann , Gisela Lorenz , Siegfried Strathmann
IPC分类号： C07C25549
CPC分类号： C07D333/24 , A01N37/52 , A01N43/10 , A01N43/56 , C07C255/53 , C07C255/54 , C07C259/18
摘要： Benzamidoxime derivatives of the formula I: where R1 is difluoromethyl or trifluoromethyl R2 is hydrogen or fluorine R3 is C1-C4-alkyl which may be substituted by cyano, C1-C4-haloalkyl, C1-C4-alkoxy-C1-C4-alkyl, C3-C6-alkenyl, C3-C6-haloalkenyl, C3-C6-alkynyl, C3-C8-cycloalkyl-C1-C4-alkyl R4 is phenyl-C1-C6-alkyl which may carry one or more substitutents selected from the group consisting of halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy and C1-C4-haloalkoxy on the phenyl ring, or is thienyl-C1-C4-alkyl which may carry one or more substituents selected from the group consisting of halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy and C1-C4-haloalkoxy on the thienyl ring, or is pyrazolyl-C1-C4-alkyl which may carry one or more substituents selected from the group consisting of halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy and C1-C4-haloalkoxy on the pyrazole ring, are prepared, and intermediates for their preparation and their use as fungicides are described.
摘要翻译：式I的苯甲酰胺肟衍生物：其中R 1是二氟甲基或三氟甲基R 2是氢或氟，R 3是可以被氰基，C 1 -C 4卤代烷基，C 1 -C 4 - 烷氧基 - C 1 -C 4 - 烷基，C 3 -C 6 - 烯基，C 3 -C 6 - 卤代烯基，C 3 -C 6 - 炔基，C 3 -C 8 - 环烷基-C 1 -C 4 - 烷基R 4是苯基-C 1 -C 6 - 或更多的选自苯基环上的卤素，C 1 -C 4 - 烷基，C 1 -C 4 - 卤代烷基，C 1 -C 4 - 烷氧基和C 1 -C 4 - 卤代烷氧基的取代基，可以携带的噻吩基-C 1 -C 4烷基一个或多个选自噻吩基环上的卤素，C 1 -C 4 - 烷基，C 1 -C 4 - 卤代烷基，C 1 -C 4 - 烷氧基和C 1 -C 4 - 卤代烷氧基的取代基，其可以是吡唑基-C 1 -C 4烷基，在吡唑环上携带一个或多个选自卤素，C 1 -C 4 - 烷基，C 1 -C 4 - 卤代烷基，C 1 -C 4 - 烷氧基和C 1 -C 4 - 卤代烷氧基的取代基，制备中间体和描述了它们作为杀真菌剂的用途。

2. 发明授权

US06509501B2 Benzamidoxime derivatives, intermediates and processes for their preparation, and their use as fungicides 失效
标题翻译：苯甲酰胺肟衍生物，中间体及其制备方法及其作为杀真菌剂的用途
公开(公告)号：US06509501B2
公开(公告)日：2003-01-21
申请号：US10093634
申请日：2002-03-11
申请人： Karl Eicken , Joachim Rheinheimer , Frank Wetterich , Eberhard Ammermann , Gisela Lorenz , Siegfried Strathmann
发明人： Karl Eicken , Joachim Rheinheimer , Frank Wetterich , Eberhard Ammermann , Gisela Lorenz , Siegfried Strathmann
IPC分类号： C07C25148
CPC分类号： C07D333/24 , A01N37/52 , A01N43/10 , A01N43/56 , C07C255/53 , C07C255/54 , C07C259/18
摘要： Benzamidoxime derivatives of the formula I where R1 is difluoromethyl or trifluoromethyl R2 is hydrogen or fluorine R3 is C1-C4-alkyl which may be substituted by cyano, C1-C4-haloalkyl, C1-C4-alkoxy-C1-C4-alkyl, C3-C6-alkenyl, C3-C6-haloalkenyl, C3-C6-alkynyl, C3-C8-cycloalkyl-C1-C4-alkyl R4 is phenyl-C1-C6-alkyl which may carry one or more substitutents selected from the group consisting of halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy and C1-C4-haloalkoxy on the phenyl ring, or is thienyl-C1-C4-alkyl which may carry one or more substituents selected from the group consisting of halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy and C1-C4-haloalkoxy on the thienyl ring, or is pyrazolyl-C1-C4-alkyl which may carry one or more substituents selected from the group consisting of halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy and C1-C4-haloalkoxy on the pyrazole ring, are prepared, and intermediates for their preparation and their use as fungicides are described.
摘要翻译：式I的苯甲酰胺肟衍生物，其中R 1是二氟甲基或三氟甲基，R 2是氢或氟，R 3是可被氰基，C 1 -C 4卤代烷基，C 1 -C 4 - 烷氧基-C 1 -C 4 - 烷基，C 3 -C 6 - 烯基，C 3 -C 6 - 卤代链烯基，C 3 -C 6 - 炔基，C 3 -C 8 - 环烷基-C 1 -C 4 - 烷基基团R 4是苯基-C 1 -C 6 - 烷基，其可以带有一个或多个选自卤素，C 1 -C 4 - 烷基，C 1 -C 4 - 卤代烷基，C 1 -C 4 - 烷氧基和C 1 -C 4 - 卤代烷氧基，可以带有一个或多个选自卤素，C 1 -C 4 - 在噻吩环上的C 1 -C 4 - 烷基，C 1 -C 4 - 卤代烷基，C 1 -C 4 - 烷氧基和C 1 -C 4 - 卤代烷氧基，可以带有一个或多个选自卤素，C 1 -C 4 - C 1-4 - 烷基，C 1 -C 4 - 卤代烷基，C 1 -C 4 - 烷氧基和C 1 -C 4 - 卤代烷氧基，并且描述了制备中间体及其作为杀真菌剂的用途。

3. 发明授权

US06420605B1 Benzamidoxim derivatives, intermediate products and methods for preparing and using them as fungicides 失效
标题翻译：苯甲酰胺衍生物，中间产物和制备和使用它们作为杀真菌剂的方法
公开(公告)号：US06420605B1
公开(公告)日：2002-07-16
申请号：US09508597
申请日：2000-03-14
申请人： Karl Eicken , Joachim Rheinheimer , Frank Wetterich , Eberhard Ammermann , Gisela Lorenz , Siegfried Strathmann
发明人： Karl Eicken , Joachim Rheinheimer , Frank Wetterich , Eberhard Ammermann , Gisela Lorenz , Siegfried Strathmann
IPC分类号： C07C23304
CPC分类号： C07D333/24 , A01N37/52 , A01N43/10 , A01N43/56 , C07C255/53 , C07C255/54 , C07C259/18
摘要： The invention relates to benzamidoxim derivatives of formula (I) wherein the substituents have the following meanings: R1 represents difluoromethyl or trifluoromethyl, R2 represents hydrogen or fluorine, R3 represents C1-C4 alkyl optionally substituted with cyano, C1-C4 halogenalkyl, C1-C4 alkoxy-C1-C4 alkyl, C3-C6 alkenyl, C3-C6 halogenalkenyl, C3-C6 alkinyl, C3-C8 cycloalkyl-C1-C4 alkyl, R4 represents phenyl-C1-C6 alkyl, which can carry one or more substituents selected from the group composed of halogen, C1-C4 alkyl, C1-C4 halogenalkyl, C1-C4 alkoxy or C1-C4 halogenalkoxy on the phenyl ring, or thienyl-C1-C4 alkyl, which can carry one or more substituents selected from the group composed of halogen, C1-C4 alkyl, C1-C4 halogenalkyl, C1-C4 halogenalkoxy on the thienyl ring, or pyrazol-C1-C4 alkyl, which can carry one or more substituents selected from the group composed of halogen, C1-C4 alkyl, C1-C4 halogenalkyl, C1-C4 alkoxy or C1-C4 halogenalkoxy on the pyrazol ring. The invention also relates to intermediate products for the preparation of these derivatives and to their use as fungicides.
摘要翻译：本发明涉及式（I）的苯甲酰氨基亚胺衍生物，其中取代基具有以下含义：R 1表示二氟甲基或三氟甲基，R 2表示氢或氟，R 3表示任选被氰基，C 1 -C 4卤代烷基，C 1 -C 4 烷氧基-C 1 -C 4烷基，C 3 -C 6烯基，C 3 -C 6卤代链烯基，C 3 -C 6炔基，C 3 -C 8环烷基-C 1 -C 4烷基，R 4表示苯基-C 1 -C 6烷基，其可以携带一个或多个选自由苯基环上的卤素，C 1 -C 4烷基，C 1 -C 4卤代烷基，C 1 -C 4烷氧基或C 1 -C 4卤代烷氧基组成的基团，或可以携带一个或多个选自组成的基团的噻吩基-C 1 -C 4烷基卤素，C 1 -C 4烷基，C 1 -C 4卤代烷基，噻吩基上的C 1 -C 4卤代烷氧基或吡唑基-C 1 -C 4烷基，其可以携带一个或多个选自卤素，C 1 -C 4烷基，吡唑环上的C 1 -C 4卤代烷基，C 1 -C 4烷氧基或C 1 -C 4卤代烷氧基。本发明还涉及用于制备这些衍生物的中间产物及其作为杀真菌剂的用途。

4. 发明授权

US06441044B1 Cycloalkyl carboxylic acid amides, their production and their use as fungicides in agriculture 失效
标题翻译：环烷基羧酸酰胺，它们的生产及其作为杀虫剂在农业中的应用
公开(公告)号：US06441044B1
公开(公告)日：2002-08-27
申请号：US09763685
申请日：2001-02-26
申请人： Ingo Rose , Frank Wetterich , Karl Eicken , Joachim Rheinheimer , Gisela Lorenz , Eberhard Ammermann , Thomas Grote , Siegfried Strathmann
发明人： Ingo Rose , Frank Wetterich , Karl Eicken , Joachim Rheinheimer , Gisela Lorenz , Eberhard Ammermann , Thomas Grote , Siegfried Strathmann
IPC分类号： A01N3718
CPC分类号： A01N53/00 , C07C233/58 , C07C255/48 , C07C271/24 , C07C2601/02
摘要： The present invention relates to cycloalkylcarboxamides of formula I where: A is optionally substituted C3-C6-cycloalkyl; Alk is straight-chain or branched C1-C6-alkylene; R1 is optionally substituted C1-C6-alkyl or C2-C6-alkenyl; R2, R3 is hydrogen, or is optionally halogenated C1-C6-alkyl or C2-C6-alkenyl; W is an optionally substituted fused bicyclic ring system having in each case six ring atoms, where one or two carbon ring atoms may be replaced by nitrogen atoms; and their agriculturally useful salts. Furthermore, the invention relates to fungicidal compositions comprising a compound of formula I as crop protection agent.
摘要翻译：本发明涉及式I的环烷基甲酰胺，其中：A为任选取代的C 3 -C 6 - 环烷基; Alk为直链或支链C 1 -C 6亚烷基; R 1为任选取代的C 1 -C 6 - 烷基或C 2 -C 6 - 烯基; R 2 ，R 3是氢，或任选被卤代的C 1 -C 6 - 烷基或C 2 -C 6 - 烯基; W是任选取代的稠合双环体系，其各自为六个环原子，其中一个或两个碳环原子可被氮取代原子及其农业上有用的盐。此外，本发明涉及杀真菌组合物，其包含式I化合物作为作物保护剂。

5. 发明授权

US06417398B1 Benzamidoxim derivatives, intermediate products and methods for preparing them, and their use as fungicides 失效
标题翻译：苯甲酰胺衍生物，中间产物及其制备方法及其作为杀真菌剂的用途
公开(公告)号：US06417398B1
公开(公告)日：2002-07-09
申请号：US09508599
申请日：2000-03-14
申请人： Karl Eicken , Joachim Rheinheimer , Frank Wetterich , Eberhard Ammermann , Gisela Lorenz , Siegfried Strathmann
发明人： Karl Eicken , Joachim Rheinheimer , Frank Wetterich , Eberhard Ammermann , Gisela Lorenz , Siegfried Strathmann
IPC分类号： C07C23305
CPC分类号： A01N43/10 , A01N37/52 , C07C259/18 , C07D333/24
摘要： The invention concerns benzamidoxim derivatives of formula (I) in which the substituents have the following meanings: R1 represents hydrogen or fluorine; R2 represents C1-C6 phenyl-alkyl, bearing on the cyclic phenyl compound one or several substituents selected in the group comprising halogen, C1-C4 alkyl, C1-C4 alkyl halide, C1-C4 alkoxy or C1-C4 alkoxy halide, or C1-C4 thienyl-alkyl, optionally bearing one or several substituents selected in the group comprising halogen, C1-C4 alkyl, C1-C4 alkyl halide, C1-C4 alkoxy or C1-C4 alkoxy or C1-C4 alkoxy halide, or C1-C4 pyrazol-alkyl, optionally bearing one or several substituents selected in the group comprising halogen, C1-C4 alkyl, C1-C4 alkyl halide, C1-C4 alkoxy or C1-C4 alkoxy halide.
摘要翻译：本发明涉及式（I）的苯甲酰氨基衍生物，其中取代基具有以下含义：R 1表示氢或氟; R2代表C1-C6苯基 - 烷基，其具有环状苯基化合物，所述取代基选自卤素，C 1 -C 4烷基，C 1 -C 4烷基卤化物，C 1 -C 4烷氧基或C 1 -C 4烷氧基卤化物，或C 1 -C 1-4噻吩基 - 烷基，任选地带有一个或几个选自以下的取代基：卤素，C 1 -C 4烷基，C 1 -C 4烷基卤，C 1 -C 4烷氧基或C 1 -C 4烷氧基或C 1 -C 4烷氧基卤化物，或C 1 -C 4 任选地带有一个或多个选自卤素，C 1 -C 4烷基，C 1 -C 4烷基卤，C 1 -C 4烷氧基或C 1 -C 4烷氧基卤基的取代基的取代基。

6. 发明授权

US6124345A Carbamoyl carboxylic acid amide oximes 失效
标题翻译：氨基甲酰基羧酰胺肟
公开(公告)号：US6124345A
公开(公告)日：2000-09-26
申请号：US147305
申请日：1998-11-24
申请人： Frank Wetterich , Karl Eicken , Reinhard Kirstgen , Eberhard Ammermann , Gisela Lorenz , Siegfried Strathmann
发明人： Frank Wetterich , Karl Eicken , Reinhard Kirstgen , Eberhard Ammermann , Gisela Lorenz , Siegfried Strathmann
IPC分类号： A01N47/12 , C07C271/22 , C07D333/28 , A01N43/06 , A01N37/12 , A01N37/18 , A01N37/44 , A01N53/00
CPC分类号： C07C271/22 , A01N47/12 , C07D333/28
摘要： The present invention relates to carbomoylcarboxamide oximes of the formula (I): ##STR1## or salts thereof, processes for preparing the carbomoylcarboxamide oximes, compositions containing the carbomoylcarboxamide oximes and processes for controlling harmful fungi with an effective amount of the carbomoylcarboxamide oximes.
摘要翻译： PCT No.PCT / EP97 / 02687第 371日期：1998年11月24日 102（e）1998年11月24日PCT PCT 1997年5月26日PCT公布。第WO97 / 46518号公报日期：1997年12月11日本发明涉及式（I）的甲酰甲酰甲酰胺肟或其盐，制备羧甲酰甲酰胺肟的方法，含有甲酰甲酰甲脒肟的组合物和有效量的甲酰甲酰甲脒肟的有害真菌控制方法。

7. 发明授权

US06265447B1 Cycloalkylalkanecarboxamides and the production and use thereof 失效
标题翻译：环烷基烷烃甲酰胺及其制备和应用
公开(公告)号：US06265447B1
公开(公告)日：2001-07-24
申请号：US09381050
申请日：1999-09-14
申请人： Frank Wetterich , Karl Eicken , Gisela Lorenz , Eberhard Ammermann , Siegfried Strathmann , Ingo Rose
发明人： Frank Wetterich , Karl Eicken , Gisela Lorenz , Eberhard Ammermann , Siegfried Strathmann , Ingo Rose
IPC分类号： A01N3718
CPC分类号： C07C255/58 , A01N37/34 , C07C255/31 , C07C2601/02 , C07C2601/08
摘要： The present invention relates to novel cycloalkylalkane-carboxamides of the formula I where the substituents have the following meanings: A is C3-C6-cycloalkyl; R1 is C1-C6-alkyl or C2-C6-alkenyl; R2, R3 and R4 are hydrogen or, independently of this meaning, have one of the meanings of the radical R1; n is 0 or 1; Y is cyano or halogen; w is phenyl, naphthyl or heteroaryl.
摘要翻译：本发明涉及式I的新的环烷基烷烃 - 甲酰胺，其中取代基具有以下含义：A为C 3 -C 6 - 环烷基; R 1为C 1 -C 6 - 烷基或C 2 -C 6 - 烯基; R 2，R 3和R 4为氢或独立于该含义，具有基团R 1的含义之一; n为0或1; Y为氰基或卤素; w为苯基，萘基或杂芳基。

8. 发明授权

US06090853A Fungicidally active carboxylic acid amides 失效
标题翻译：杀真菌活性羧酸酰胺
公开(公告)号：US06090853A
公开(公告)日：2000-07-18
申请号：US155099
申请日：1998-09-21
申请人： Frank Wetterich , Oliver Wagner , Karl Eicken , Eberhard Ammermann , Siegfried Strathmann , Gisela Lorenz , John-Bryan Speakman
发明人： Frank Wetterich , Oliver Wagner , Karl Eicken , Eberhard Ammermann , Siegfried Strathmann , Gisela Lorenz , John-Bryan Speakman
IPC分类号： C07C231/02 , A01N37/18 , A01N37/34 , C07C233/58 , C07C233/59 , C07C233/60 , C07C253/30 , C07C255/47 , C07C255/60
CPC分类号： C07C233/59 , C07C233/58 , C07C233/60 , C07C255/47 , C07C255/60 , C07C2102/42 , C07C2103/68 , C07C2103/74
摘要： Carboxamides of the formula I ##STR1## where the substituents have the following meanings: R.sup.1 is unsubstituted or substituted bicycloalkyl, tricycloalkyl or bicycloalkenyl;R.sup.2,R.sup.3 and R.sup.4 are each, independently of one another, hydrogen, or unsubstituted or substituted: alkyl, cycloalkyl, cycloalkenyl or heterocyclyl;Ar is unsubstituted or substituted aryl or hetaryl,but excluding 2-cyano-N-[1-(1-naphthyl)ethyl]-3-phenyl-bicyclo[2.2.1]hept-5-ene-2-carboxamide, a process for their preparation, compositions comprising compounds I and the use of compounds I for preparing the compositions, and further a process for controlling harmful fungi and the use of the compounds I for this purpose.
摘要翻译： PCT No.PCT / EP97 / 01161 Sec。 371日期：1998年9月21日 102（e）1998年9月21日PCT PCT 1997年3月7日PCT公布。公开号WO97 / 35838 日期1997年10月2日具有下列含义的式I的酰胺：R1是未取代的或取代的双环烷基，三环烷基或双环烯基; R2，R3和R4彼此独立地为氢，或未取代或取代的：烷基，环烷基，环烯基或杂环基; Ar是未取代或取代的芳基或杂芳基，但不包括2-氰基-N- [1-（1-萘基）乙基] -3-苯基 - 双环[2.2.1]庚-5-烯-2-甲酰胺，用于制备组合物，包含化合物I的组合物和化合物I用于制备组合物的用途，以及用于控制有害真菌的方法和用于该目的的化合物I的用途。

9. 发明授权

US6156778A Agents for controlling harmful fungi 失效
标题翻译：用于控制有害真菌的药剂
公开(公告)号：US6156778A
公开(公告)日：2000-12-05
申请号：US242729
申请日：1999-02-22
申请人： Ruth Muller , Herbert Bayer , Hubert Sauter , Karl Eicken , Frank Wetterich , Eberhard Ammermann , Gisela Lorenz , Siegfried Strathmann , Maria Scherer , Klaus Schelberger , Bernd Muller , Joachim Leyendecker
发明人： Ruth Muller , Herbert Bayer , Hubert Sauter , Karl Eicken , Frank Wetterich , Eberhard Ammermann , Gisela Lorenz , Siegfried Strathmann , Maria Scherer , Klaus Schelberger , Bernd Muller , Joachim Leyendecker
IPC分类号： A01N37/52 , A01N47/12 , A01N47/24 , A01N43/56 , A01N43/64 , A01N47/10
CPC分类号： A01N47/12 , A01N47/24
摘要： This invention relates to a composition for controlling harmful fungi comprising, in a solid or liquid carrier,a) at least one carbamate of the formula I ##STR1## where X is CH or N andthe radicals R.sup.a and R.sup.b independently of one another are a hydrogen atom, a halogen atom, a C.sub.1 -C.sub.4 -alkyl or a C.sub.1 -C.sub.4 -haloalkyl group; andb) at least one valine amide of the formula II ##STR2## where R.sup.1 is C.sub.3 -C.sub.4 -alkyl andR.sup.2 is naphthyl or phenyl, the phenyl radical being substituted in the 4-position by a halogen atom, a C.sub.1 -C.sub.4 -alkyl group or C.sub.1 -C.sub.4 -alkoxy group.
摘要翻译： PCT No.PCT / EP97 / 04679 Sec。一九九九年二月二十二日 102（e）1999年2月22日PCT 1997年8月27日PCT PCT。公开号WO98 / 08386 日本特开1998年5月3日本发明涉及一种用于控制有害真菌的组合物，其在固体或液体载体中包含：a）至少一种式I的氨基甲酸酯，其中X为CH或N，基团R a和R b彼此独立地为氢原子，卤素原子，C1-C4烷基或C1-C4卤代烷基; 和b）至少一种式II的缬氨酸酰胺，其中R 1是C 3 -C 4 - 烷基，R 2是萘基或苯基，苯基在4-位被卤素原子取代，C 1 -C 4 - 烷基或 C1-C4-烷氧基。

10. 发明授权

US6069144A N-heterocyclic compounds, intermediate products used to prepare them, agents containing them and their use in antifungal applications 失效
标题翻译： N-杂环化合物，用于制备它们的中间产物，含有它们的试剂及其在抗真菌应用中的用途
公开(公告)号：US6069144A
公开(公告)日：2000-05-30
申请号：US11610
申请日：1998-02-12
申请人： Oliver Wagner , Frank Wetterich , Karl Eicken , Michael Rack , Gerhard Hamprecht , Gunther Lamm , John-Bryan Speakman , Gisela Lorenz , Eberhard Ammermann , Siegfried Strathmann
发明人： Oliver Wagner , Frank Wetterich , Karl Eicken , Michael Rack , Gerhard Hamprecht , Gunther Lamm , John-Bryan Speakman , Gisela Lorenz , Eberhard Ammermann , Siegfried Strathmann
IPC分类号： A01N43/40 , A01N43/42 , A01N43/54 , A01N43/78 , A01N43/90 , C07D213/70 , C07D213/71 , C07D213/82 , C07D213/85 , C07D215/54 , C07D239/38 , C07D277/74 , C07D277/76 , C07D513/04 , A01N43/58 , A61K31/505 , C07D211/36 , C07D215/16 , C07D515/02
CPC分类号： C07D213/70 , A01N43/40 , A01N43/42 , A01N43/54 , A01N43/78 , A01N43/90 , C07D213/71 , C07D213/82 , C07D213/85 , C07D215/54 , C07D239/38 , C07D277/74 , C07D277/76 , C07D513/04
摘要： N-heterocyclic compounds I ##STR1## or their salts or N-oxides, wherein A is an N-heterocycle selected from the group consisting of ##STR2## R.sup.1 -R.sup.6, R.sup.24 -R.sup.26 are hydrogen, cyano, nitro, halogen, aminocarbonyl, methylsulfonyl, alkyl, haloalkyl, alkoxy, haloalkoxy, alkylthio, alkoxyalkyl, alkoxycarbonyl, aryl or aryloxy;m is 0, 1 or 2;Alk is optionally substituted 1,2-ethylidene, 1,3-propylidene cycloalkyl or cycloalkenyl;X is oxygen or sulfur;Q is optionally substituted aryl, cycloalkyl, cycloalkenyl, or arylalkyl;their manufacture and suitable intermediates therefore, as well as compositions comprising them and their use for controlling harmful fungi.
摘要翻译： PCT No.PCT / EP96 / 03680 Sec。 371日期1998年2月12日 102（e）1998年2月12日PCT PCT 1996年8月21日PCT公布。公开号WO97 / 08147 日期1997年3月6日N-杂环化合物I或其盐或N-氧化物，其中A为选自由R 1 -R 6，R 24-R 26组成的组的N-杂环为氢，氰基，硝基，卤素，氨基羰基，甲基磺酰基烷基，卤代烷基，烷氧基，卤代烷氧基，烷硫基，烷氧基烷基，烷氧基羰基，芳基或芳氧基; m为0,1或2; Alk是任选取代的1,2-亚乙基，1,3-亚丙基环烷基或环烯基; X是氧或硫; Q是任选取代的芳基，环烷基，环烯基或芳基烷基; 因此它们的制造和合适的中间体，以及包含它们的组合物及其用于控制有害真菌的用途。

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