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1. 发明授权

US5096903A Fungicidal trisubstituted 1,2,4-triazine-3,5-diones 失效
标题翻译：杀真菌剂分解的1,2,4-三嗪-3,5-二酮
公开(公告)号：US5096903A
公开(公告)日：1992-03-17
申请号：US644049
申请日：1991-01-18
申请人： Hermann Uhr , Arno Widdig , Dieter Berg , Gerd Hanssler
发明人： Hermann Uhr , Arno Widdig , Dieter Berg , Gerd Hanssler
IPC分类号： A01N43/707 , C07D253/06 , C07D253/075
CPC分类号： C07D253/075 , A01N43/707
摘要： Fungicidal trisubstituted 1,2,4-triazine-3,5-diones of the formula ##STR1## in which Ar represents optionally substituted aryl,R.sup.1 represents an optionally substituted aliphatic of cycloaliphatic radical andR.sup.2 represents an optionally substituted aliphatic radical.Many of the intermediates therefor where R.sup.2 is hydrogen and/or the 3-O is replaced by 3-S are also new.
摘要翻译：式（I）的杀真菌三取代的1,2,4-三嗪-3,5-二酮，其中Ar表示任选取代的芳基，R 1表示任选取代的脂环族基团，R 2表示任选取代的脂族基团。其中R2是氢和/或3-O被3-S替代的许多中间体也是新的。

2. 发明授权

US5077291A Fungicidal trisubstituted 1,3,5-triazine-2,4,6-triones 失效
标题翻译：杀真菌剂1,3,5-三嗪-2,4,6-TRIONES
公开(公告)号：US5077291A
公开(公告)日：1991-12-31
申请号：US585433
申请日：1990-09-20
申请人： Hermann Uhr , Alfons Adler , Arno Widdig , Hermann Hagemann , Gerd Hanssler
发明人： Hermann Uhr , Alfons Adler , Arno Widdig , Hermann Hagemann , Gerd Hanssler
IPC分类号： C07D251/34 , A01N43/64 , C07C275/24 , C07D251/30
CPC分类号： C07D251/30
摘要： Fungicidal trisubstituted 1,3,5-triazine-2,4,6-triones of the formula ##STR1## in which R.sup.1, R.sup.2 and R.sup.3 are different radicals andR.sup.1 represents an optionally substituted aliphatic or cycloaliphatic radical,R.sup.2 represents an optionally substituted aliphatic radical andR.sup.3 represents an optionally substituted aralkyl radical.
摘要翻译： R 1，R 2和R 3是不同基团并且R 1表示任选取代的脂族或脂环族基团的式（I）的杀真菌三取代的1,3,5-三嗪-2,4,6-三酮，其中R2表示任选取代的脂族基，R 3表示任选取代的芳烷基。

3. 发明授权

US4927824A Fungicidal trisubstituted 1,3,5-triazine-2,4,6-triones 失效
标题翻译：杀真菌三取代1,3,5-三嗪-2,4,6-三硝基苯
公开(公告)号：US4927824A
公开(公告)日：1990-05-22
申请号：US324948
申请日：1989-03-17
申请人： Alfons Adler , Arno Widdig , Engelbert Kuhle , Wolfgang Fuhrer , Hermann Hagemann , Gerd Hanssler
发明人： Alfons Adler , Arno Widdig , Engelbert Kuhle , Wolfgang Fuhrer , Hermann Hagemann , Gerd Hanssler
IPC分类号： A01N43/64 , A01N43/74 , A01N43/80 , A01N43/82 , A01N43/832 , A01N43/88 , C07D401/04 , C07D403/04 , C07D405/04 , C07D409/04 , C07D411/04 , C07D413/04 , C07D417/04 , C07D419/04
CPC分类号： C07D401/04 , A01N43/64 , A01N43/74 , A01N43/80 , A01N43/82 , A01N43/88 , C07D403/04 , C07D405/04 , C07D409/04 , C07D411/04 , C07D413/04 , C07D417/04
摘要： Fungicidal trisubstituted 1,3,5-triazine-2,4,6-triones of the formula ##STR1## in which R.sup.1 stands for an optionally substituted aliphatic, aromatic or cycloaliphatic radical,R.sup.2 stands for an optionally substituted aliphatic radical andR.sup.3 stands for optionally substituted, heterocyclically fused phenyl.
摘要翻译：式（I）的杀真菌三取代1,3,5-三嗪-2,4,6-三酮，其中R 1表示任选取代的脂族，芳族或脂环族基团，R 2表示任选取代的脂族基团， R3表示任选取代的杂环稠合的苯基。

4. 发明授权

US5350861A Substituted 3-aryl-pyrrolidine-2,4-diones 失效
标题翻译：取代的3-芳基 - 吡咯烷-2,4-二酮
公开(公告)号：US5350861A
公开(公告)日：1994-09-27
申请号：US821801
申请日：1992-01-16
申请人： Reiner Fischer , Hermann Uhr , Arno Widdig , Stefan Dutzmann , Christoph Erdelen , Ulrike Wachendorff-Neumann , Klaus Schaller
发明人： Reiner Fischer , Hermann Uhr , Arno Widdig , Stefan Dutzmann , Christoph Erdelen , Ulrike Wachendorff-Neumann , Klaus Schaller
IPC分类号： A01N43/36 , A61K31/40 , A61P31/00 , A61P31/04 , C07D207/36 , C07D207/38 , C07D401/12 , C07D403/12 , C07D417/12 , C07D207/40
CPC分类号： A01N43/36 , C07D207/38
摘要： There are provided new substituted 3-aryl-pyrrolidine-2,4-diones of the formula ##STR1## in which X represents hydrogen, alkyl, halogen or alkoxy,Y represents hydrogen, alkyl, halogen, alkoxy or halogenoalkyl,Z represents alkyl, halogen or alkoxy,n represents a number from 0-3,R represents hydrogen or the groups--CO--R.sup.1, --CO--O--R.sup.2 in whichR.sup.1 and R.sup.2 have the meanings given in the text of the application,A represents optionally halogen-substituted alkyl, alkenyl, alkinyl, alkoxyalkyl, polyalkoxyalkyl, alkylthioalkyl and cycloalkyl which is optionally interrupted by hetero atoms, or represents arylakyl which is optionally substituted by halogen, alkyl, halogenoalkyl, alkoxy or nitro,B represents optionally substituted aryl or benzyl.The new compounds of the formula (I) have highly pronounced insecticidal, acaricidal, fungicidal and antimycotic properties.
摘要翻译：提供新的式（Ⅰ）取代的3-芳基 - 吡咯烷-2,4-二酮，其中X代表氢，烷基，卤素或烷氧基，Y代表氢，烷基，卤素，烷氧基或卤代烷基，Z 表示烷基，卤素或烷氧基，n表示0-3的数，R表示氢或基团-CO-R1，-CO-O-R2，其中R1和R2具有本申请案文中给出的含义，A 代表任选被卤素取代的烷基，烯基，炔基，烷氧基烷基，聚烷氧基烷基，烷硫基烷基和任选被杂原子间隔的环烷基，或表示任选被卤素，烷基，卤代烷基，烷氧基或硝基取代的芳基，B表示任选取代的芳基或苄基。式（I）的新化合物具有非常显着的杀虫，杀螨，杀真菌和抗真菌性质。

5. 发明授权

US06486343B1 Substituted phenyl keto enols as pesticides and herbicides 失效
标题翻译：取代的苯基酮基作为农药和除草剂
公开(公告)号：US06486343B1
公开(公告)日：2002-11-26
申请号：US10074351
申请日：2002-02-12
申请人： Volker Lieb , Hermann Hagemann , Arno Widdig , Michael Ruther , Reiner Fischer , Thomas Bretschneider , Christoph Erdelen , Ulrike Wachendorff-Neumann , Alan Graff , Udo Schneider
发明人： Volker Lieb , Hermann Hagemann , Arno Widdig , Michael Ruther , Reiner Fischer , Thomas Bretschneider , Christoph Erdelen , Ulrike Wachendorff-Neumann , Alan Graff , Udo Schneider
IPC分类号： C07C22900
CPC分类号： C07D309/38 , A01N37/36 , A01N37/46 , A01N43/08 , A01N43/12 , A01N43/16 , A01N43/36 , A01N43/38 , A01N43/40 , A01N43/90 , A01N47/06 , C07C57/30 , C07C57/34 , C07C59/84 , C07C69/65 , C07C69/757 , C07C323/56 , C07D207/38 , C07D209/96 , C07D307/94 , C07D311/74 , C07D311/96 , C07D333/50 , C07D405/04 , C07D405/14 , C07D491/10 , C07D493/04
摘要： The present invention relates to novel compounds of the formula (I) in which Het represents one of the groups in which A, B, D, G, V, W, X, Y and Z are as defined in the description, processes and intermediates for their preparation, and to their use as pesticides and herbicides.
摘要翻译：本发明涉及式（I）的新型化合物，其中Het表示A，B，D，G，V，W，X，Y和Z中的一个基团，其描述，方法和中间体如准备和用作农药和除草剂。

6. 发明授权

US06380246B1 Alkyl-dihalogenated phenyl-substituted ketoenols useful as pesticides and herbicides 失效
标题翻译：用作农药和除草剂的烷基 - 二卤代苯基取代的酮戊二醇
公开(公告)号：US06380246B1
公开(公告)日：2002-04-30
申请号：US09404424
申请日：1999-09-23
申请人： Folker Lieb , Hermann Hagemann , Arno Widdig , Michael Ruther , Reiner Fischer , Thomas Bretschneider , Christoph Erdelen , Ulrike Wachendorff-Neumann , Peter Dahmen , Markus Dollinger , Hans-Joachim Santel , Alan Graff , Wolfram Andersch , Norbert Mencke , Andreas Turberg
发明人： Folker Lieb , Hermann Hagemann , Arno Widdig , Michael Ruther , Reiner Fischer , Thomas Bretschneider , Christoph Erdelen , Ulrike Wachendorff-Neumann , Peter Dahmen , Markus Dollinger , Hans-Joachim Santel , Alan Graff , Wolfram Andersch , Norbert Mencke , Andreas Turberg
IPC分类号： A61K3134
CPC分类号： C07D333/50 , A01N43/10 , A01N43/12 , A01N43/16 , A01N43/36 , A01N43/38 , A01N43/40 , A01N43/90 , A01N47/02 , A01N47/06 , A01N53/00 , C07C69/757 , C07C323/56 , C07D207/38 , C07D209/54 , C07D307/94 , C07D309/08 , C07D309/36 , C07D311/46 , C07D333/32 , C07D333/38 , C07D491/10 , C07D493/10
摘要： The present invention relates to new compounds of the formula (I) in which X represents halogen, Y represents halogen or alkyl and Z represents halogen or alkyl, with the proviso that always one of the radicals Y and Z represents halogen while the other represents alkyl, and Het represents one of the groups in which A, B, D and G have the meanings given in the description, to a plurality of processes for their preparation and to their use as pesticides and herbicides.
摘要翻译：本发明涉及式（I）的新化合物，其中X表示卤素，Y表示卤素或烷基，Z表示卤素或烷基，条件是基团Y和Z中的任何一个表示卤素，而另一个表示烷基，并且Het 代表其中A，B，D和G具有本说明书给出的含义的组之一，其制备方法和用作农药和除草剂的多种方法。

7. 发明授权

US5994274A Dialkyl phenyl halide-substituted keto-enols for use as herbicides and pesticides 失效
标题翻译：用作除草剂和杀虫剂的二烷基苯基卤化物取代的酮 - 烯醇
公开(公告)号：US5994274A
公开(公告)日：1999-11-30
申请号：US981610
申请日：1997-12-23
申请人： Reiner Fischer , Thomas Bretschneider , Hermann Hagemann , Folker Lieb , Michael Ruther , Arno Widdig , Peter Dahmen , Markus Dollinger , Christoph Erdelen , Hans-Joachim Santel , Ulrike Wachendorff-Neumann , Alan Graff , Wolfram Andersch
发明人： Reiner Fischer , Thomas Bretschneider , Hermann Hagemann , Folker Lieb , Michael Ruther , Arno Widdig , Peter Dahmen , Markus Dollinger , Christoph Erdelen , Hans-Joachim Santel , Ulrike Wachendorff-Neumann , Alan Graff , Wolfram Andersch
IPC分类号： A01N43/08 , A01N43/10 , A01N43/36 , A01N43/86 , C07D207/38 , C07D209/54 , C07D209/96 , C07D231/32 , C07D279/06 , C07D307/60 , C07D307/94 , C07D309/28 , C07D309/32 , C07D333/32 , C07D405/04 , C07D407/04 , C07D409/04 , C07D417/04 , C07D487/04 , C07D491/107 , C07D493/10 , C07D495/10 , C07D513/04 , A01N43/56 , C07D207/333 , C07D231/36
CPC分类号： C07D333/32 , C07D207/38 , C07D279/06 , C07D307/60 , C07D309/32
摘要： The present invention relates to new compounds of the formula (I) ##STR1## in which X represents alkyl,Y represents halogen or alkyl andZ represents halogen or alkyl,with the proviso that one of the radicals Y and Z always represents halogen and the other alkyl,Het represents one of the groups ##STR2## in which A, B, D and G have the meanings given in the description,a plurality of processes for their preparation and their use as pesticides and herbicides.
摘要翻译： PCT No.PCT / EP96 / 02601 Sec。 371 1997年12月23日第 102（e）1997年12月23日PCT PCT 1996年6月17日PCT公布。公开号WO97 / 02243 日期：1997年1月23日本发明涉及式（I）的新化合物，其中X表示烷基，Y表示卤素或烷基，Z表示卤素或烷基，条件是基团Y和Z之一始终表示卤素而另一个烷基Het代表其中A，B，D和G具有本说明书中给出的含义的一组，其制备方法及其作为农药和除草剂的用途。

8. 发明授权

US4261988A Chromanone derivatives 失效
标题翻译：色酮衍生物
公开(公告)号：US4261988A
公开(公告)日：1981-04-14
申请号：US20119
申请日：1979-03-13
申请人： Arno Widdig , Hans-Joachim Kabbe , Martin Scheer , Rudiger Sitt
发明人： Arno Widdig , Hans-Joachim Kabbe , Martin Scheer , Rudiger Sitt
IPC分类号： A61K31/35 , A61K31/352 , A61P19/06 , C07D311/22 , C07D311/24 , C07D311/32 , C07D311/92 , C07D311/96 , C07D405/04 , C07D491/10 , C07D491/107
CPC分类号： C07D491/10 , C07D311/22 , C07D311/24 , C07D311/32 , C07D311/92 , C07D311/96
摘要： Compounds useful in the treatment of cholesterolaemia are of the general formula ##STR1## or salts thereof in which R.sup.1 and R.sup.2 independently denote radicals including hydrogen, alkyl, aryl and heterocyclic radical or together complete a carbocyclic or heterocylic ring, R.sup.3 denotes a radical ##STR2## in which R.sup.9, R.sup.10 and R.sup.11 include hydrogen, cyano, nitro, alkyl and aryl or, in pairs, complete carbocyclic rings, X denotes cyano, nitro or substituted carbonyl, sulphonyl or phosphonyl group, R.sup.4 is hydrogen or a radical defined for R.sup.1 or R.sup.3, and R.sup.5, R.sup.6, R.sup.7 and R.sup.8 include hydrogen, nitro, cyano, carboxyl, alkyl and aryl or, in pairs, complete carbocyclic rings, with the proviso that R.sup.1 and R.sup.9 are not both phenyl if X denotes CO--C.sub.6 H.sub.6. The compounds exhibit considerably higher hypocholesterolaemic activity than the known clofibrate and in addition exhibit a pronounced nutritive effect, e.g., in a medicated fodder or premix.
摘要翻译：用于治疗胆固醇血症的化合物具有通式（I）或其盐，其中R 1和R 2独立地表示包括氢，烷基，芳基和杂环基团的基团，或者一起完成碳环或杂环，R3表示其中R9，R10和R11包括氢，氰基，硝基，烷基和芳基，或成对地成为完全碳环，X表示氰基，硝基或取代的羰基，磺酰基或膦酰基，R4是氢或基团对于R 1或R 3而言，R 5，R 6，R 7和R 8包括氢，硝基，氰基，羧基，烷基和芳基，或成对地成为完全碳环，条件是如果X表示CO，则R 1和R 9不是苯基 -C6H6。化合物显示比已知的氯贝特明显更高的降血胆固醇血症活性，并且还显示出明显的营养作用，例如在药物饲料或预混物中。

9. 发明授权

US4005123A Substituted phenylisothioureas and processes for their preparation and use 失效
标题翻译：取代苯基异硫脲及其制备和使用方法
公开(公告)号：US4005123A
公开(公告)日：1977-01-25
申请号：US595040
申请日：1975-07-11
申请人： Heinrich Kolling , Herbert Thomas , Arno Widdig , Hartmund Wollweber
发明人： Heinrich Kolling , Herbert Thomas , Arno Widdig , Hartmund Wollweber
IPC分类号： A61K31/17 , A61K31/155 , C07C67/00 , C07C325/00 , C07C335/38 , C07C149/40
CPC分类号： C07C335/38
摘要： N-[2-(Substituted amido)phenyl]-N'-carbonyl-S-substituted isothioureas bearing an optionally substituted phenoxy, phenylthio, phenylsulfinyl or phenylsulfonyl group in the 4- or 5-position of the 2-(substituted amido)-phenyl group are anthelmintic agents. The compounds, of which N-(2-acetamido-4-phenoxyphenyl)-N'-carbomethoxy-S-methylthiourea is a typical example, are prepared through the reaction of S-substituted N-(mercaptohalomethylene)carbamic acid ester and an apropriately substituted 2-aminoanilide, or through alkylation of the corresponding S-unsubstituted thiourea.
摘要翻译：在2-（取代的酰胺基） - 苯并噻唑的4-或5-位上带有任选取代的苯氧基，苯硫基，苯基亚磺酰基或苯基磺酰基的N- [2-（取代的酰氨基）苯基] -N'-羰基-S-取代的异硫脲，苯基是驱肠剂。通过S-取代的N-（巯基甲基亚甲基）氨基甲酸酯和适当的反应制备N-（2-乙酰氨基-4-苯氧基苯基）-N'-甲酯基-S-甲基硫脲的化合物是典型的例子取代的2-氨基苯胺，或通过相应的S-未取代的硫脲的烷基化。

10. 发明授权

US3972905A Quinonemonoxime-arylacylhydrazones 失效
标题翻译：喹诺酮肟 - 芳基酰腙
公开(公告)号：US3972905A
公开(公告)日：1976-08-03
申请号：US553874
申请日：1975-02-27
申请人： Arno Widdig , Ewald Urbschat, deceased , Ferdinand Grewe , Helmut Kaspers
发明人： Arno Widdig , Ewald Urbschat, deceased , Ferdinand Grewe , Helmut Kaspers
IPC分类号： A01N37/28 , A01N20060101 , A01N37/10 , A01N37/34 , A01N37/48 , C07C20060101 , C07C67/00 , C07C239/00 , C07C251/44 , C07C313/00 , C07C323/60 , C07C131/00 , C07C149/42
CPC分类号： C07C251/84
摘要： Quinonemonoxime-arylacylhydrazones of the formula ##EQU1## in which EACH X independently is halogen, nitro, C.sub.1 -C.sub.6 alkyl or C.sub.1 -C.sub.6 alkoxy,Ar is phenyl or naphthyl,Z is oxygen or sulfur,R is hydrogen, C.sub.1 -C.sub.6 alkyl, hydroxyl or C.sub.1 -C.sub.6 alkoxy,Each Y independently is C.sub.1 -C.sub.6 alkyl,n is 0, 1, 2, 3 or 4,m is 0 or 1, andq is 0, 1 or 2Which possess fungicidal properties.
摘要翻译：硝基，肟基 - 芳基酰腙，其中每个X独立地为卤素，硝基，C 1 -C 6烷基或C 1 -C 6烷氧基，Ar为苯基或萘基，式R 1（X）-Xn-Ar-Zm-CH-CO-NH- Z是氧或硫，R是氢，C 1 -C 6烷基，羟基或C 1 -C 6烷氧基，每个Y独立地是C 1 -C 6烷基，N 1 O 0,1,2,3或4，M是0或1，和 Q IS 0，1或2，具有正确的防伪特性。

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