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21. 发明授权

US5883250A Substituted azadioxacycloalkenes, fungicidal composition containing them, process for preparing them, and method of using them to combat fungi 失效
标题翻译：取代的azadioxacycalkalkene，含有它们的杀真菌组合物，其制备方法和使用它们对抗真菌的方法
公开(公告)号：US5883250A
公开(公告)日：1999-03-16
申请号：US857119
申请日：1997-05-15
申请人： Bernd-Wieland Kruger , Lutz Assmann , Herbert Gayer , Peter Gerdes , Ulrich Heinemann , Dietmar Kuhnt , Ulrich Philipp , Thomas Seitz , Jorg Stetter , Ralf Tiemann , Heinz-Wilhelm Dehne , Stefan Dutzmann , Gerd Hanssler
发明人： Bernd-Wieland Kruger , Lutz Assmann , Herbert Gayer , Peter Gerdes , Ulrich Heinemann , Dietmar Kuhnt , Ulrich Philipp , Thomas Seitz , Jorg Stetter , Ralf Tiemann , Heinz-Wilhelm Dehne , Stefan Dutzmann , Gerd Hanssler
IPC分类号： A01N43/72 , A01N43/78 , A01N43/836 , A01N43/88 , C07D273/00 , C07D273/01 , C07D409/12 , C07D413/06 , C07D413/12 , C07D413/14 , C07D417/12 , C07D417/14 , C07D273/06 , C07D269/00
CPC分类号： C07D273/00 , A01N43/88 , C07D409/12 , C07D413/06 , C07D413/12 , C07D413/14 , C07D417/12 , C07D417/14
摘要： New azadioxacycloalkenes of the formula (I): ##STR1## wherein Z, G, Ar, E and A are as defined herein, fungicidal compositions containing them, processes for preparing them, and methods of using them to combat fungi.
摘要翻译：式（I）的新的氮杂二环烷基烯烃：其中Z，G，Ar，E和A如本文所定义，含有它们的杀真菌组合物，其制备方法和使用它们来对抗真菌的方法。

22. 发明授权

US5736551A Fungicidal compositions 失效
公开(公告)号：US5736551A
公开(公告)日：1998-04-07
申请号：US787599
申请日：1997-01-22
申请人： Stefan Dutzmann , Heinz-Wilhelm Dehne , Karl-Heinz Kuck , Wilhelm Brandes , Wolfgang Kramer
发明人： Stefan Dutzmann , Heinz-Wilhelm Dehne , Karl-Heinz Kuck , Wilhelm Brandes , Wolfgang Kramer
IPC分类号： A01N31/02 , A01N33/08 , A01N33/18 , A01N33/22 , A01N37/18 , A01N37/22 , A01N37/34 , A01N43/28 , A01N43/30 , A01N43/36 , A01N43/38 , A01N43/40 , A01N43/50 , A01N43/54 , A01N43/653 , A01N43/66 , A01N43/76 , A01N43/84 , A01N43/90 , A01N47/38 , A01N47/40 , A01N47/42 , A01N47/44 , A01N53/12 , A01N55/00 , A01N55/10 , A01N59/02 , A01N59/06 , A01N59/16 , A01N59/20 , A01N43/26
CPC分类号： A01N43/30
摘要： A novel fungicidal composition comprising a fungicidally effective amount of a combination consisting of (A) the known aminomethyl heterocycle of the formula ##STR1## and (B) at least one other known fungicidally active compound selected from the group mentioned in the specification. The novel compositions show a synergistic activity.

23. 发明授权

US5728737A N-alkoxy-amidine derivatives 失效
标题翻译： N-烷氧基 - 脒衍生物及其作为农药的用途
公开(公告)号：US5728737A
公开(公告)日：1998-03-17
申请号：US776225
申请日：1997-01-23
申请人： Ulrich Heinemann , Bernd-Wieland Kruger , Ralf Tiemann , Stefan Dutzmann , Klaus Stenzel
发明人： Ulrich Heinemann , Bernd-Wieland Kruger , Ralf Tiemann , Stefan Dutzmann , Klaus Stenzel
IPC分类号： A01N37/52 , A01N43/836 , C07C257/12 , C07C259/14 , C07C317/44 , C07C323/50 , C07C327/40 , C07D239/52 , C07D239/56 , C07D285/08 , C07D401/12 , C07D417/04 , A01N37/18 , A01N43/54 , A01N43/82 , C07C233/64 , C07C257/18 , C07D239/02
CPC分类号： C07D239/56 , A01N37/52 , C07C257/12 , C07C259/14 , C07D239/52 , C07D285/08 , C07D401/12 , C07D417/04
摘要： The present invention relates to novel N-alkoxy-arnidine derivatives of the formula (I), to a process for their preparation and to their use as pesticides. In addition, the invention also relates to novel intermediates and to a process for their preparation. ##STR1##
摘要翻译： PCT No.PCT / EP95 / 02797 371日期1997年1月23日 102（e）日期1997年1月23日PCT提交1995年7月17日PCT公布。公开号WO96 / 04239 日期：1996年2月15日本发明涉及式（I）的新型N-烷氧基 - 吖啶衍生物，其制备方法及其作为农药的用途。此外，本发明还涉及新型中间体及其制备方法。（一）

24. 发明授权

US5530149A Azolylmethyl-fluorocyclopropyl derivatives 失效
公开(公告)号：US5530149A
公开(公告)日：1996-06-25
申请号：US462730
申请日：1995-06-05
申请人： Jurgen Scherkenbeck , Thomas Himmler , Stefan Bohm , Hermann Hagemann , Klaus Stroech , Stefan Dutzmann , Heinz-Wilhelm Dehne , Gerd Hanssler
发明人： Jurgen Scherkenbeck , Thomas Himmler , Stefan Bohm , Hermann Hagemann , Klaus Stroech , Stefan Dutzmann , Heinz-Wilhelm Dehne , Gerd Hanssler
IPC分类号： A01N43/653 , C07D249/08 , C07D301/02 , C07D303/08 , C07D303/18 , C07D303/20 , C07D521/00
CPC分类号： C07D249/08 , A01N43/653 , C07D231/12 , C07D233/56
摘要： New azolylmethyl-fluorocyclopropyl derivatives of the formula ##STR1## in which R represents ##STR2## and addition products thereof which acids or metal salts are very effective for combating fungi.New oxiranes of the formula ##STR3## in which R has the abovementioned meaning, are valuable intermediates for the preparation of compounds of the formula (I).

25. 发明授权

US5516749A Herbicidal and fungicidal substituted triazolinones 失效
标题翻译：除草和杀真菌剂取代的三唑啉酮
公开(公告)号：US5516749A
公开(公告)日：1996-05-14
申请号：US180721
申请日：1994-01-13
申请人： Klaus-Helmut Muller , Klaus Konig , Kurt Findeisen , Hans-Joachim Santel , Klaus Lurssen , Robert R. Schmidt , Stefan Dutzmann
发明人： Klaus-Helmut Muller , Klaus Konig , Kurt Findeisen , Hans-Joachim Santel , Klaus Lurssen , Robert R. Schmidt , Stefan Dutzmann
IPC分类号： A01N47/38 , C07D249/12 , C07D249/14 , C07D405/04 , C07D405/06 , C07D405/12 , A01N43/653
CPC分类号： C07D405/04 , A01N47/38 , C07D249/12 , C07D405/06 , C07D405/12
摘要： Herbicidal and fungicidal substituted triazolinones of the formula ##STR1## in which R.sup.1 represents hydrogen, alkyl alkenyl, alkinyl, halogenoalkyl, halogenoalkenyl, halogenoalkinyl, alkoxyalkyl, cycloalkyl or cycloalkylalkyl, of represents tetrahydrofuranyl or tetrahydrofuranylalkyl, or represents in each case optionally substituted aralkyl or aryl,R.sup.2 represents hydrogen, alkyl, alkenyl, alkinyl, halogenoalkyl, halogenoalkenyl, halogenoalkinyl, cyanoalkyl, hydroxyalkyl, alkoxyalkyl, aryloxyalkyl, alkoxycarbonylalkyl, alkoxycarbonylalkenyl, alkylaminoalkyl or dialkylaminoalkyl, or represents in each case optionally substituted cyclocalkyl, cycloalkylalkyl, cycloalkenyl or cycloalkenylalkyl, or represents optionally substituted heterocyclyalkyl, or represents in each case optionally substituted aralkyl, aroyl, aryl, aralkyloxy or aryloxy, or represents alkoxy, alkenyloxy or alkinyloxy,R.sup.3 represents alkyl, alkenyl, alkinyl, halogenoalkyl, halogenoalkenyl, halogenoalkinyl, cyanoalkyl, alkoxyalkyl or alkylthioalkyl, or represents in each case optionally substituted cycloalkyl, cycloalkylalkyl, aryl or aralkyl,X represents oxygen or sulphur andY represents oxygen or sulphur,and new intermediates.
摘要翻译：其中R1代表氢，烷基烯基，炔基，卤代烷基，卤代烯基，卤代烯基，烷氧基烷基，环烷基或环烷基烷基的式（Ⅰ）的除草和杀真菌的取代的三唑啉酮代表四氢呋喃基或四氢呋喃基烷基，或代表在各种情况下任选取代芳烷基或芳基，R 2表示氢，烷基，烯基，炔基，卤代烷基，卤代烯基，卤代烯基，氰基烷基，羟基烷基，烷氧基烷基，芳氧基烷基，烷氧基羰基烷基，烷氧基羰基烯基，烷基氨基烷基或二烷基氨基烷基，或在各种情况下表示任选取代的环烷基，环烷基烷基，环烯基或环烯基或代表任选取代的杂环烷基，或在每种情况下表示任选取代的芳烷基，芳酰基，芳基，芳烷氧基或芳氧基，或表示烷氧基，烯氧基或烷氧基，R3表示烷基，烯基，炔基，卤代烷基，卤代烯基，卤代烯基，氰基烷基，烷氧基烷基或烷硫基烷基，或在每种情况下表示任选取代的环烷基，环烷基烷基，芳基或芳烷基，X表示氧或硫，Y表示氧或硫，以及新的中间体。

26. 发明授权

US5493034A Intermediate for pesticidal aminomethylheterocyclic compounds 失效
公开(公告)号：US5493034A
公开(公告)日：1996-02-20
申请号：US443522
申请日：1995-05-18
申请人： Wolfgang Kramer , Joachim Weissmuller , Dieter Berg , Wilhelm Brandes , Stefan Dutzmann
发明人： Wolfgang Kramer , Joachim Weissmuller , Dieter Berg , Wilhelm Brandes , Stefan Dutzmann
IPC分类号： A01N43/28 , A01N43/30 , C07D317/72 , C07D327/04 , C07D411/12
CPC分类号： C07D317/72 , A01N43/28 , A01N43/30 , C07D327/04 , C07D411/12
摘要： Fungicidally active compounds of the formula ##STR1## in which X represents oxygen or sulphur,R represents cycloalkyl, or represents optionally substituted aryl, or represents the radical ##STR2## R.sup.1 and R.sup.2 each independently is hydrogen or an organic radical, or together with the nitrogen atom form a heterocyclic radical,R.sup.3 represents hydrogen, alkyl or optionally substituted aryl, andR.sup.4 represents alkyl or cycloalkyl, or represents optionally substituted aryl,but wherein R.sup.3 and R.sup.4 may not simultaneously represent methyl,and acid addition salts thereof, as well as intermediates therefor.

27. 发明授权

US5428073A Antimicrobial agents which are substituted 2-cyclohexan-1-yl-amine compounds. 失效
标题翻译：作为取代的2-环己烷-1-基 - 胺化合物的抗微生物剂。
公开(公告)号：US5428073A
公开(公告)日：1995-06-27
申请号：US956535
申请日：1992-10-05
申请人： Franz Kunisch , Peter Babczinski , Dieter Arlt , Wilhelm Brandes , Heinz-Wilhelm Dehne , Stefan Dutzmann , Manfred Plempel
发明人： Franz Kunisch , Peter Babczinski , Dieter Arlt , Wilhelm Brandes , Heinz-Wilhelm Dehne , Stefan Dutzmann , Manfred Plempel
IPC分类号： C07D275/06 , A01N37/44 , A01N37/46 , A01N43/38 , A01N43/40 , A01N43/80 , B01J23/46 , C07B61/00 , C07C219/24 , C07C227/16 , C07C229/48 , C07C233/52 , C07C237/04 , C07C237/24 , C07C269/06 , C07C271/24 , C07C323/53 , C07C323/62 , C07C327/24 , C07C327/32 , C07D213/30 , C07F9/165 , C07F9/40 , A61K31/19
CPC分类号： C07D213/30 , A01N37/44 , A01N37/46 , A01N43/40 , C07C229/48 , C07C233/52 , C07C237/04 , C07C237/24 , C07C271/24 , C07C327/24 , C07C327/32 , C07F9/4021 , C07C2101/08 , Y02P20/55
摘要： There are described new 2-cyclohexan-1-yl-amine derivatives of formula (I) ##STR1## in which A, R.sup.1, R.sup.2, R.sup.3 and R.sup.4 have the meaning given in the description, and processes for their preparation.The compounds of the formula (I) are used as anti-microbial agents.
摘要翻译：描述了式（I）的新的2-环己烷-1-基 - 胺衍生物其中A，R1，R2，R3和R4具有说明书中给出的含义及其制备方法。式（I）的化合物用作抗微生物剂。

28. 发明授权

US5416088A Substituted pyridylpyrimidines, their preparation and their use 失效
标题翻译：取代的吡啶基嘧啶，其制备及其用途
公开(公告)号：US5416088A
公开(公告)日：1995-05-16
申请号：US107670
申请日：1993-08-16
申请人： Ulrich Heinemann , Heinz-Wilhelm Dehne , Stefan Dutzmann , Christoph Erdelen
发明人： Ulrich Heinemann , Heinz-Wilhelm Dehne , Stefan Dutzmann , Christoph Erdelen
IPC分类号： A01N25/02 , A01N25/30 , A01N43/54 , C07C225/14 , C07C225/16 , C07C323/27 , C07D401/04
CPC分类号： C07D401/04 , A01N43/54 , C07C225/14 , C07C225/16 , C07C323/27
摘要： ##STR1## Substituted pyridylpyrimidines have formula (I), in which A and Ar have the meaning given in the test of the description. Also disclosed are their preparation, their use and new initial products. The compounds having formula (I) may be prepared from appropriate salts of 2-pyridylamidine with appropriate enamines; said enamines are also new and disclosed by the invention, and may be prepared from appropriate ketones with appropriate formaldehyde derivates.
摘要翻译： PCT No.PCT / EP92 / 00311 Sec。 371日期：1993年8月16日 102（e）日期1993年8月16日PCT提交1992年2月13日PCT公布。第WO92 / 14726号公报（I）取代的吡啶基嘧啶具有式（I），其中A和Ar具有在描述试验中给出的含义。还披露了他们的准备，使用和新的初始产品。具有式（I）的化合物可以由适当的2-吡啶基脒盐与适当的烯胺制备; 所述烯胺也是新的并且由本发明公开，并且可以由具有合适的甲醛衍生物的合适的酮制备。

29. 发明授权

US5371065A Substituted azolylmethyloxiranes 失效
标题翻译：取代的唑基甲基环氧乙烷
公开(公告)号：US5371065A
公开(公告)日：1994-12-06
申请号：US305836
申请日：1989-02-02
申请人： Hans-Ludwig Elbe , Karl H. Buchel , Wilhelm Brandes , Stefan Dutzmann , Klaus Lurssen
发明人： Hans-Ludwig Elbe , Karl H. Buchel , Wilhelm Brandes , Stefan Dutzmann , Klaus Lurssen
IPC分类号： C07D405/06 , A01N43/50 , A01N43/653 , C07D233/60 , C07D249/08 , C07D521/00
CPC分类号： C07D249/08 , A01N43/50 , A01N43/653 , C07D231/12 , C07D233/56
摘要： Fungicidal and plant growth-regulating substituted azolylmethyloxiranes of the formula ##STR1## in which R.sup.1 stands for alkyl,R.sup.2 stands for alkyl,X stands for a nitrogen atom or the CH group,Y stands (or halogen, alkyl, cycloalkyl, alkoxy, alkylthio, halogenoalkyl, halogenoalkoxy, halogenoalkylthio, optionally substituted phenyl, optionally substituted phenoxy, optionally substituted phenylalkyl and/or optionally substituted phenylalkoxy andm stands for the numbers 0, 1, 2 or 3,and addition products thereof with acids and metal salts.
摘要翻译： R 1代表烷基，R 2代表烷基，X代表氮原子或CH基团，Y代表（或卤素，烷基，环烷基，环烷基，环烷基或芳烷基）的杀真菌和植物生长调节取代的吡唑基甲基环氧烷，烷氧基，烷硫基，卤代烷基，卤代烷氧基，卤代烷硫基，任选取代的苯基，任选取代的苯氧基，任选取代的苯基烷基和/或任选取代的苯基烷氧基，m代表数字0,1,2或3，其加成产物与酸和金属盐。

30. 发明授权

US5334608A Azolymethyl-cyclopropyl derivatives 失效
标题翻译：芳基甲基 - 环丙基衍生物
公开(公告)号：US5334608A
公开(公告)日：1994-08-02
申请号：US021390
申请日：1993-02-23
申请人： Jurgen Scherkenbeck , Thomas Himmler , Hermann Hagemann , Stefan Dutzmann , Heinz-Wilhelm Dehne , Gerd Hanssler
发明人： Jurgen Scherkenbeck , Thomas Himmler , Hermann Hagemann , Stefan Dutzmann , Heinz-Wilhelm Dehne , Gerd Hanssler
IPC分类号： A01N53/12 , A01N43/653 , A01N53/04 , A61K31/41 , C07D249/08 , C07D301/02 , C07D303/46 , C07D521/00
CPC分类号： C07D249/08 , A01N43/653 , C07D231/12 , C07D233/56 , C07D303/46
摘要： New azolylmethyl-cyclopropyl derivatives of the formula ##STR1## in which R represents cyano or a group of the formula ##STR2## Z represents halogen, alkyl having 1 to 4 carbon atoms, halogenoalkyl having 1 to 4 carbon atoms and 1 to 5 halogen atoms, alkoxy having 1 to 4 carbon atoms, halogenoalkoxy having 1 to 4 carbon atoms and 1 to 5 halogen atoms, or alkoximininoalkyl having 1 to 4 carbon atoms in the alkoxy group and 1 to 4 carbon atoms in the alkyl group andm represents the numbers 0, 1 or 2, and addition products thereof with acids or metal salts are very effective for combating fungi.New oxiranes of the formula ##STR3## in which Z and m have the abovementioned meanings, are valuable intermediates for the preparation of compounds of the formula (I).
摘要翻译：其中R表示氰基的式（I）的新的唑基甲基 - 环丙基衍生物或下式的基团Z表示卤素，具有1至4个碳原子的烷基，具有1至4个碳原子的卤代烷基和1至 5个卤素原子，1〜4个碳原子的烷氧基，1〜4个碳原子的卤代烷氧基和1〜5个卤素原子，烷氧基中1〜4个碳原子的烷基肟基，烷基中1〜4个碳原子代表数字0,1或2，其与酸或金属盐的加成产物对抗真菌非常有效。其中Z和m具有上述含义的式“IMAGE”（II）的新环氧烷是制备式（I）化合物的有价值的中间体。

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