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1. 发明授权

US06664295B2 Fungicidal phenylamidine derivatives 失效
标题翻译：杀真菌苯脒衍生物
公开(公告)号：US06664295B2
公开(公告)日：2003-12-16
申请号：US09923146
申请日：2001-08-06
申请人： Vincent Gerusz , Darren James Mansfield , Joseph Perez , Jean-Pierre Vors , Derek Baldwin , Thomas Lawley Hough , Robert Dale Mitchell
发明人： Vincent Gerusz , Darren James Mansfield , Joseph Perez , Jean-Pierre Vors , Derek Baldwin , Thomas Lawley Hough , Robert Dale Mitchell
IPC分类号： A01N3302
CPC分类号： C07C261/04 , A01N37/52 , A01N47/40 , C07C257/12
摘要： The invention provides fungicidal compounds of formula I and salts thereof: wherein the various radicals and substituents are as defined in the description, fungicidal compositions containing them and method for combating fungi which comprises applying these.
摘要翻译：本发明提供了式I的杀真菌化合物及其盐：其中各种基团和取代基如说明书中所定义，含有它们的杀真菌组合物和抗真菌方法包括应用它们。

2. 发明授权

US06696487B2 Fungicidal phenyl(thio)urea and phenyl(thio)carbamate derivatives 失效
标题翻译：杀真菌苯基（硫代）脲和苯基（硫代）氨基甲酸酯衍生物
公开(公告)号：US06696487B2
公开(公告)日：2004-02-24
申请号：US09923124
申请日：2001-08-06
申请人： Vincent Gerusz , Darren James Mansfield , José Perez , David Tickle , Jean-Pierre Vors , Derek Baldwin , Thomas Lawley Hough , Dale Robert Mitchell
发明人： Vincent Gerusz , Darren James Mansfield , José Perez , David Tickle , Jean-Pierre Vors , Derek Baldwin , Thomas Lawley Hough , Dale Robert Mitchell
IPC分类号： A01N4710
CPC分类号： C07D209/48 , A01N43/64 , A01N43/78 , A01N43/88 , A01N47/20 , A01N47/30 , A01N47/32 , A01N47/34 , A01N47/38 , C07C271/28 , C07C275/36 , C07C275/64 , C07C281/06 , C07C311/49 , C07C333/24 , C07C335/18 , C07C335/40 , C07C337/06 , C07C2601/02 , C07D207/09 , C07D213/61 , C07D213/75 , C07D213/77 , C07D235/14 , C07D239/42 , C07D271/06 , C07D271/10 , C07D285/08 , C07D295/21 , C07D295/32 , C07D307/20 , C07D307/68 , C07D317/58
摘要： The invention relates to compounds of formula (I), and also to salts thereof, which have fungicidal activities: in which the various radicals and substituents are as defined in the description, and also to the fungicidal compositions containing them and to methods for combating the phytopathogenic fungi of crops using these compounds and compositions.
摘要翻译：本发明涉及具有杀真菌活性的式（I）化合物及其盐，其中各种基团和取代基如说明书中所定义，还涉及含有它们的杀真菌组合物，以及用于防治使用这些化合物和组合物的作物的植物病原真菌。

3. 发明授权

US06541630B1 Fungicides 失效
标题翻译：杀菌剂
公开(公告)号：US06541630B1
公开(公告)日：2003-04-01
申请号：US10172891
申请日：2002-06-13
申请人： John Frederick Atherall , Thomas Lawley Hough , Stephen David Lindell , Mary Josephine O'Mahony , John Henry Parsons , Elizabeth Anne Saville-Stones
发明人： John Frederick Atherall , Thomas Lawley Hough , Stephen David Lindell , Mary Josephine O'Mahony , John Henry Parsons , Elizabeth Anne Saville-Stones
IPC分类号： C07D49504
CPC分类号： C07D495/04 , A01N43/90
摘要： The invention provides the use in combating fungi of compounds of general formula I wherein R1 is hydrogen, hydroxy, acyl, acyloxy, optionally substituted amino, Ra, Ra3Si, RaS or RaO, where Ra is optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted cycloalkyl, optionally substituted cycloalkenyl, optionally substituted aryl or optionally substituted heterocyclyl; Z is oxygen or sulfur; M is a thiophene ring; and R3 and R4, which may be the same or different, have the same meaning as Ra or can be optionally substituted amino, hydrogen, halogen, cyano, nitro or a group ORc or S(O)mRc, where Rc has the same meaning as Ra or is hydrogen or acyl and m is 0, 1 or 2; or R3 and R4 together with the atoms to which they are attached form an optionally substituted carbocyclic or heterocyclic ring; together with tautomers of compounds where R1 is hydrogen.
摘要翻译：本发明提供了用于对抗通式I化合物的用途，其中R 1是氢，羟基，酰基，酰氧基，任选取代的氨基，R a，R 3 Si，RaS或RaO，其中R a是任选取代的烷基，任选取代的链烯基，炔基，任选取代的环烷基，任选取代的环烯基，任选取代的芳基或任选取代的杂环基; Z是氧或硫; M是噻吩环; 和R 3和R 4可以相同或不同，具有与R a相同的含义或可以是任选取代的氨基，氢，卤素，氰基，硝基或基团OR c或S（O）m R c，其中R c具有相同的含义为Ra或为氢或酰基，m为0,1或2; 或R 3和R 4与它们所连接的原子一起形成任选取代的碳环或杂环; 以及R1为氢的化合物的互变异构体。

4. 发明授权

US06893650B1 N2-phenylamidine derivatives 有权
标题翻译： N2-苯基脒衍生物
公开(公告)号：US06893650B1
公开(公告)日：2005-05-17
申请号：US09890775
申请日：2000-02-04
申请人： Mark David Charles , Wilfried Franke , David Eric Green , Thomas Lawley Hough , Dale Robert Mitchell , Donald James Simpson , John Frederick Atherall
发明人： Mark David Charles , Wilfried Franke , David Eric Green , Thomas Lawley Hough , Dale Robert Mitchell , Donald James Simpson , John Frederick Atherall
IPC分类号： C07D249/08 , A01N25/02 , A01N37/52 , A01N41/10 , A01N43/06 , A01N43/18 , A01N43/40 , A01N43/54 , A01N43/74 , A01N43/76 , A01N43/80 , A01N43/82 , A01N43/836 , A01N43/84 , A01N43/88 , A01N43/90 , A01N47/42 , A01P3/00 , C07C233/37 , C07C251/04 , C07C257/12 , C07C257/14 , C07C317/40 , C07C323/20 , C07C323/41 , C07D207/325 , C07D207/50 , C07D209/48 , C07D213/64 , C07D213/68 , C07D215/22 , C07D237/14 , C07D237/16 , C07D239/34 , C07D239/46 , C07D239/88 , C07D241/24 , C07D251/30 , C07D251/34 , C07D257/04 , C07D261/08 , C07D261/14 , C07D263/38 , C07D263/46 , C07D263/58 , C07D271/06 , C07D271/10 , C07D273/00 , C07D277/20 , C07D277/34 , C07D277/68 , C07D285/00 , C07D285/08 , C07D285/10 , C07D285/12 , C07D285/13 , C07D295/12 , C07D295/125 , C07D307/12 , C07D307/81 , C07D307/83 , C07D311/22 , C07D311/56 , C07D317/64 , C07D333/16 , C07D333/20 , C07D333/28 , C07D333/54 , C07D333/58 , C07D333/64 , C07D487/04 , C07D495/04 , C07F7/08 , A61K31/155 , C07D237/00 , C07D261/20 , C07D233/37
CPC分类号： C07D209/48 , A01N37/52 , A01N43/06 , A01N43/40 , A01N43/54 , A01N43/74 , A01N43/82 , A01N43/90 , A01N47/42 , C07C257/12 , C07C257/14 , C07D207/50 , C07D239/88 , C07D251/34 , C07D261/08 , C07D263/38 , C07D263/46 , C07D263/58 , C07D271/06 , C07D271/10 , C07D285/08 , C07D285/13 , C07D295/125 , C07D311/22 , C07D333/54 , C07D487/04 , C07D495/04 , C07F7/0812
摘要： The invention provides fungicidal compounds of formula (I) and salts thereof wherein: R1 is alkyl, alkenyl, alkynyl, carbocyclyl or heterocyclyl, each of which may be substituted, or hydrogen; R2 and R3, which may be the same or different, are any group defined for R1; cyano; acyl; —ORa or —SRa, where Ra is alkyl, alkenyl, alkynyl, carbocyclyl or heterocyclyl, each of which may be substituted; or R2 and R3, or R2 and R1, together with their interconnecting atoms may form a ring, which may be substituted; R4 is alkyl, alkenyl, alkynyl, carbocyclyl or heterocyclyl, each of which may be substituted; hydroxy; mercapto; azido; nitro; halogen; cyano; acyl; optionally substituted amino; cyanato; thiocyanato; —SF5; —ORa; —SRa or —Si(Ra)3; m is 0 to 3; when present R5, which may be the same or different to any other R5, is any group defined for R4; R6 is optionally substituted carbo- or heterocylclyl; and A is a defined linking group, or —A—R6 and R5 together with benzene ring M form an optionally substituted fused ring system.
摘要翻译：本发明提供式（I）的杀真菌化合物及其盐，其中：R 1是烷基，烯基，炔基，碳环基或杂环基，其各自可以被取代，或氢; R 2和R 3可以相同或不同，为R 1定义的任何基团; 氰基酰基; 其中R a是烷基，烯基，炔基，碳环基或杂环基，其各自可以被取代;或者其中R a，或R 2和R 3，或R 2和R 1以及它们的互连原子可以形成环，其可以被取代; R 4是烷基，烯基，炔基，碳环基或杂环基，其各自可以被取代; 羟基; 巯基叠氮硝基卤素; 氰基酰基; 任选取代的氨基; 青色硫氰酸 -SF 5; -OR ^{a ; -SR ^{a或-Si（R a a）3 3; m为0〜3; 当存在R 5可以与任何其它R 5相同或不同时，R 5为限定的任何基团。 R 6是任选取代的碳 - 或杂环基; 并且A是限定的连接基团，或者-A-R 6和R 5和苯环M一起形成任选取代的稠环体系。}}

5. 发明授权

US06432964B1 Fungicides 失效
标题翻译：杀菌剂
公开(公告)号：US06432964B1
公开(公告)日：2002-08-13
申请号：US09423135
申请日：1999-11-05
申请人： John Frederick Atherall , Thomas Lawley Hough , Stephen David Lindell , Mary Josephine O'Mahony , John Henry Parsons , Elizabeth Anne Saville-Stones
发明人： John Frederick Atherall , Thomas Lawley Hough , Stephen David Lindell , Mary Josephine O'Mahony , John Henry Parsons , Elizabeth Anne Saville-Stones
IPC分类号： A01N4390
CPC分类号： C07D495/04 , A01N43/90
摘要： The invention provides the use in combating fungi of compounds of general formula (I) wherein R1 is hydrogen, hydroxy, acyl, acyloxy, optionally substituted amino, Ra, Ra3Si, RaS or RaO, where Ra is optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted cycloalkyl, optionally substituted cycloalkenyl, optionally substituted aryl or optionally substituted heterocyclyl; R2 has the same meaning as Ra or can be hydrogen; Z is oxygen or sulfur, M is a thiophene ring, and R3 and R4, which may be the same or different, have the same meaning as Ra or can be optionally substituted amino, hydrogen, halogen, cyano, nitro or a group ORc or S(O)mRc, where Rc has the same meaning as Ra or is hydrogen or acyl and m is 0, 1 or 2; or R3 and R4 together with the atoms to which they are attached form an optionally substituted carbocyclic or heterocyclic ring; together with tautomers of compounds where R1 is hydrogen.
摘要翻译：本发明提供了用于对抗通式（I）的化合物的用途，其中R 1是氢，羟基，酰基，酰氧基，任选取代的氨基，Ra，Ra 3 Si，RaS或RaO，其中R a是任选取代的烷基，任选取代的链烯基，任选取代的炔基，任选取代的环烷基，任选取代的环烯基，任选取代的芳基或任选取代的杂环基; R2具有与Ra相同的含义，也可以是氢; Z是氧或硫，M是噻吩环，并且可以相同或不同的R 3和R 4具有与R a相同的含义或可以是任选取代的氨基，氢，卤素，氰基，硝基或基团OR c或 S（O）m R c，其中R c具有与R a相同的含义或氢或酰基，m为0,1或2; 或R 3和R 4与它们所连接的原子一起形成任选取代的碳环或杂环; 以及R1为氢的化合物的互变异构体。

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