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1. 发明申请

WO2004048316A1 N-ALKYNYL-2- (SUBSTITUTED PHENOXY) ALKYLAMIDES AND THEIR USE AS FUNGICIDES 审中-公开
标题翻译： N-烷基-2-（取代的苯氧基）烷基胺及其作为杀真菌剂的用途
公开(公告)号：WO2004048316A1
公开(公告)日：2004-06-10
申请号：PCT/GB2003/004834
申请日：2003-11-10
申请人： SYNGENTA LIMITED , SALMON, Roger , LANGTON, David, William
发明人： SALMON, Roger , LANGTON, David, William
IPC分类号： C07C235/20
CPC分类号： C07C235/20 , A01N39/02 , A01N39/04
摘要： Fungicidal compounds of the general formula (1) wherein X, Y, Z, R 1 , R 2 , R 3 , R 4 and R 5 have the definitions given in claim 1.
摘要翻译：通式（1）的杀真菌化合物，其中X，Y，Z，R 1，R 2，R 3，R 4和R 5具有权利要求1中给出的定义。

2. 发明申请

WO2010116122A3 HERBICIDAL QUINOLINE AND 1,8 -NAPHTHYRIDINE COMPOUNDS 审中-公开
公开(公告)号：WO2010116122A3
公开(公告)日：2010-10-14
申请号：PCT/GB2010/000638
申请日：2010-03-31
申请人： SYNGENTA LIMITED , SALMON, Roger , MITCHELL, Glynn , MORRIS, James, Alan
发明人： SALMON, Roger , MITCHELL, Glynn , MORRIS, James, Alan
IPC分类号： C07D471/04 , C07D215/227 , A01N43/90
摘要： The present invention relates to novel herbicidal oxopyridine and thionopyridine derivatives of Formula (I), or an agronomically acceptable salt of said compound wherein R 1 , R 5 , R 6 , R 7 , X 1 , X 2 and Q are as defined herein. The invention further relates to processes and intermediates for the preparation of the oxopyridine derivatives, to compositions which comprise the herbicidal compounds, and to their use for controlling weeds, in particular in crops of useful plants.

3. 发明申请

WO2009115788A1 HERBICIDAL COUMPOUNDS 审中-公开
标题翻译：除草剂
公开(公告)号：WO2009115788A1
公开(公告)日：2009-09-24
申请号：PCT/GB2009/000713
申请日：2009-03-16
申请人： SYNGENTA LIMITED , MITCHELL, Glynn , SALMON, Roger , BACON, David, Philip , ASPINALL, Ian, Henry , BRIGGS, Emma , AVERY, Alaric, James , MORRIS, James, Alan , RUSSELL, Claire, Janet
发明人： MITCHELL, Glynn , SALMON, Roger , BACON, David, Philip , ASPINALL, Ian, Henry , BRIGGS, Emma , AVERY, Alaric, James , MORRIS, James, Alan , RUSSELL, Claire, Janet
IPC分类号： A01N43/90 , A01P13/00 , C07D471/04
CPC分类号： A01N43/90 , C07D471/04
摘要： The present invention relates to novel herbicidal [l,8]-naphthyridines of Formula (Ia) or (Ib), or an agronomically acceptable salt of said compound wherein R 2 , R 3 , R 4 , R 5 ,R 6 ,R 7 , R 8 , n, m, X and Q are as defined herein. The invention further relates to processes and intermediates for the preparation of the [l,8]-naphthyridines, to compositions which comprise the herbicidal compounds, and to their use for controlling weeds, in particular in crops of useful plants.
摘要翻译：本发明涉及式（Ia）或（Ib）的新型除草[1,8] - 萘啶或所述化合物的农业上可接受的盐，其中R 2，R 3，R 4，R 5，R 6，R 7，R 8，n，m ，X和Q如本文所定义。本发明还涉及用于制备[1,8] - 萘啶的方法和中间体，其包含除草化合物的组合物，以及其用于防治杂草的用途，特别是在有用植物的作物中。

4. 发明申请

WO2004108694A1 N-ALKYNYL-2-HETEROARYLOXYALKYLAMIDES FOR USE AS FUNGICIDES 审中-公开
标题翻译：用作杀真菌剂的N-烷基-2-杂环戊烯基甲酰胺
公开(公告)号：WO2004108694A1
公开(公告)日：2004-12-16
申请号：PCT/GB2004/002308
申请日：2004-05-28
申请人： SYNGENTA LIMITED , SALMON, Roger , CROWLEY, Patrick, Jelf
发明人： SALMON, Roger , CROWLEY, Patrick, Jelf
IPC分类号： C07D277/62
CPC分类号： C07D263/56 , A01N43/76 , A01N43/78 , C07D277/62 , C07D277/68 , C07D277/82 , C07D413/12 , C07D417/12
摘要： Compounds of the general formula (I) are useful as fungicides wherein Het is a 5- or 6- linked group of the formula (a) or (b), and the variables are as defined in the claims.
摘要翻译：通式（I）的化合物可用作杀真菌剂，其中Het是式（a）或（b）的5-或6-连接基团，并且变量如权利要求中所定义。

5. 发明申请

WO2006058699A1 1-ALKYNYL-2-ARYLOXYALKYLAMIDES AND THEIR USE AS FUNGICIDES 审中-公开
标题翻译： 1-烷基-2-芳基甲酰胺及其作为杀真菌剂的用途
公开(公告)号：WO2006058699A1
公开(公告)日：2006-06-08
申请号：PCT/EP2005/012734
申请日：2005-11-29
申请人： SYNGENTA PARTICIPATIONS AG , SYNGENTA LIMITED , CROWLEY, Patrick, Jelf , SALMON, Roger , CHRYSTAL, Ewan, James, Turner , SAGEOT, Olivia, Anabelle , QUARANTA, Laura , BRUNNER, Hans-Georg , BEAUDEGNIES, Renaud , CEDERBAUM, Fredrik , MURPHY KESSABI, Fiona
发明人： CROWLEY, Patrick, Jelf , SALMON, Roger , CHRYSTAL, Ewan, James, Turner , SAGEOT, Olivia, Anabelle , QUARANTA, Laura , BRUNNER, Hans-Georg , BEAUDEGNIES, Renaud , CEDERBAUM, Fredrik , MURPHY KESSABI, Fiona
IPC分类号： C07D307/91 , C07D333/76 , C07D215/20 , A01N39/02 , A01N43/00
CPC分类号： C07D307/91 , A01N39/04 , A01N41/10 , A01N43/12 , A01N43/30 , A01N43/42 , A01N43/78 , C07D215/20 , C07D327/04 , C07D333/76
摘要： Compounds of the formula wherein the substituents are as defined in the claims, are useful as fungicides.
摘要翻译：下式的化合物其中取代基如权利要求中所定义，可用作杀真菌剂。

6. 发明申请

WO2004048315A1 FUNGICIDES 审中-公开
标题翻译：杀菌剂
公开(公告)号：WO2004048315A1
公开(公告)日：2004-06-10
申请号：PCT/GB2003/004832
申请日：2003-11-10
申请人： SYNGENTA LIMITED , SALMON, Roger , CROWLEY, Patrick, Jelf , BACON, David, Philip
发明人： SALMON, Roger , CROWLEY, Patrick, Jelf , BACON, David, Philip
IPC分类号： C07C235/20
CPC分类号： C07D249/08 , A01N39/04 , C07C235/20 , C07C255/30 , C07C317/28 , C07C323/41
摘要： Fungicidal compounds of the general formula (1): wherein X, Y and Z are independently H, halogen, C l-4 alkyl, halo(C 1-4 )alkyl, C 2-4 alkenyl, halo(C 2 - 4 )alkenyl, C24 alkynyl, halo(C 2-4 )alkynyl, C 1 _ 4 alkoxy, halo(C 1-4 )alkoxy, -S(O) n (C 1-4 )alkyl where n is 0, 1 or 2 and the alkyl group is optionally substituted with fluoro, -OS0 2 (C 1-4 )alkyl where the alkyl group is optionally substituted with fluoro, cyano, nitro, C, 1-4 alkoxycarbonyl, -CONR'R", -COR', -NR'COR" or -NR'COOR"' where R' and R" are independently H or C 1-4 alkyl and R"' is C l-4 alkyl, provided that at least one of X and Z is other than H; R 1 is C l - 4 alkyl, C 2-4 alkenyl or C 2-4 alkynyl in which the alkyl, alkenyl and alkynyl groups are optionally substituted on their terminal carbon atom with one, two or three halogen atoms, with a cyano group, with a C 1-4 alkylcarbonyl group, with a C 1-4 alkoxycarbonyl group or with a hydroxy group; R 2 is H, C 1-4 alkyl, C 1-4 alkoxymethyl or benzyloxymethyl in which the phenyl ring of the benzyl moiety is optionally substituted with CI-4 alkoxy; R 3 and R 4 are independently H, C 1-3 alkyl, C 2-3 alkenyl or C 2-3 alkynyl provided that both are not H and that when both are other than H their combined total of carbon atoms does not exceed 4, or R 3 and R 4 join with the carbon atom to which they are attached to form a 3 or 4 membered carbocyclic ring optionally containing one 0, S or N atom and optionally substituted with halo or C 1-4 alkyl; and R 5 is unsubstituted C 3-4 alkyl, unsubstituted C 3-6 cycloalkyl or C l-4 alkyl or C 3-6 cycloalkyl in which the alkyl and cycloalkyl groups are substituted with halo, hydroxy, C 1-6 alkoxy, cyano, C 1-4 alkylcarbonyloxy, aminocarbonyloxy, mono- or di(C 1 _ 4 )alkylaminocarbonyloxy, -S(O)"(C 1-6 )alkyl where n is 0, 1 or 2, triazolyl, tri(C 1-4 )alkylsilyloxy, optionally substituted phenoxy, optionally substituted thienyloxy, optionally substituted benzyloxy or optionally substituted thienyl-methoxy, in which the optionally substituted phenyl and thienyl rings of phenoxy, thienyloxy, benzyloxy and thienylmethoxy are optionally substituted with one, two or three substituents selected from halo, hydroxy, mercapto, C 1-4 alkyl, C 2-4 alkenyl, C 2-4 alkynyl, C1-4 alkoxy, C 2-4 alkenyloxy, C 2-4 alkynyloxy, halo(C 1-4 )alkyl, halo(C 1-4 )alkoxy, C 1-4 alkylthio; halo(C 1-4 )alkylthio, hydroxy(C 1-4 )alkyl, C 1-4 alkoxy(C 1-4 )alkyl, C 3-6 cycloalkyl, C 3-6 cycloalkyl(C 1-4 )alkyl, phenoxy, benzyloxy, benzoyloxy, cyano, isocyano, thiocyanato, isothiocyanato, nitro, -NR - R', -NHCOR m , -NHCONR m R", -CONRmR", -S02R m , -OS02R m , -COR M , -CR'=NR" or -N=CR m R", in which R"' and R" are independently hydrogen, CI-4 alkyl, halo(C 1-4 )alkyl, C1-4 alkoxy, halo(C 1-4 )alkoxy, C 1-4 alkylthio, C 3-6 cycloalkyl, C 3-6 cycloalkyl(C 1-4 )alkyl, phenyl or benzyl, the phenyl and benzyl groups being optionally substituted with halogen, C 1-4 alkyl or C 1-4 alkoxy.
摘要翻译：通式（1）的杀真菌化合物：其中X，Y和Z独立地为H，卤素，C 1-4烷基，卤代（C 1-4）烷基，C 2-4烯基，卤代（C 2-4）烯基，C 24炔基，卤素（C 2-4）炔基，C 1-4烷氧基，卤代（C 1-4）烷氧基，-S（O）n（C 1-4）烷基，其中n为0,1或2，烷基任选被氟取代， -OCO 2（C 1-4）烷基，其中烷基任选被氟，氰基，硝基，C 1-4烷氧基羰基，-CONR'R“，-COR'，-NR'COR”或-NR'COOR“ 其中R'和R“独立地是H或C 1-4烷基，R”'是C 1-4烷基，条件是X和Z中的至少一个不是H; R 1是C 1-4烷基，C 2-4烯基或C2-4炔基，其中烷基，烯基和炔基在其末端碳原子上任选被一个，两个或三个卤素原子与氰基，C 1-4烷基羰基和C 1-4烷氧基羰基基团或羟基; R 2是H，C 1-4烷基，C 1-4烷氧基甲基或苄氧基甲基，其中苄基部分任选被C 1-4烷氧基取代; R3和R4分别是H，C1-3烷基，C2-3烯基或C2-3炔基，条件是两者都不是H，当两者都不是H时，它们的总碳原子数不超过4，或者R3和R4 与它们所连接的碳原子一起形成任选含有一个O，S或N原子并任选被卤素或C 1-4烷基取代的3或4元碳环; R5是未取代的C3-4烷基，未取代的C3-6环烷基或C1-C4烷基或C3-6环烷基，其中烷基和环烷基被卤素，羟基，C1-6烷氧基，氰基，C1-4烷基羰基氧基，氨基羰基氧基，单或二（C 1-4）烷基氨基羰基氧基，-S（O）“（C 1-6）烷基，其中n为0,1或2，三唑基，三（C 1-4）烷基甲硅烷氧基，任选取代的苯氧基，任选取代的噻吩氧基，任选取代的苄氧基或任选取代的噻吩基 - 甲氧基，其中苯氧基，噻吩氧基，苄氧基和噻吩基甲氧基的任选取代的苯基和噻吩环任选被一个，两个或三个选自卤素，羟基，巯基，C 1-4烷基， C 2-4烷氧基，C 2-4烷氧基，C 2-4烷氧基，卤代（C 1-4）烷基，卤代（C 1-4）烷氧基，C 1-4烷硫基;卤代（C1- 4）烷硫基，羟基（C 1-4）烷基，C 1-4烷氧基（C 1-4）烷基，C 3-6环烷基，C 3-6环烷基（C 1-4）烷基，苯氧基，苄氧基，苯甲酰氧基，氰基，异氰酸，硫氰酸酯，异硫氰酸酯，硝基，-NR'R'，-NHCOR m，-NHCONR m R“，-CONRmR”，-SO 2 R m，-OSO 2 R m，-COR M >，-CR'= NR“或

7. 发明申请

WO2004047537A1 FUNGICIDES 审中-公开
标题翻译：杀菌剂
公开(公告)号：WO2004047537A1
公开(公告)日：2004-06-10
申请号：PCT/GB2003/004565
申请日：2003-10-22
申请人： SYNGENTA LIMITED , SALMON, Roger
发明人： SALMON, Roger
IPC分类号： A01N39/04
CPC分类号： A01N39/04
摘要： The use as a plant fungicide of a compound of the general formula (I): wherein X and Y are both chloro, bromo or methyl or X is methoxy and Y is cyano; R 1 is ethyl or n -propyl and R 2 is methyl or ethyl. The compounds (1), other than those where X and Y are both chloro or methyl and R 1 is ethyl, are novel.
摘要翻译：用作通式（I）化合物的植物杀真菌剂：其中X和Y都是氯，溴或甲基，或X是甲氧基，Y是氰基; R1是乙基或正丙基，R2是甲基或乙基。除了X和Y都是氯或甲基，R1是乙基的化合物（1）是新的。

8. 发明申请

WO2003048128A1 PYRIDYLOXYALKANOIC ACID AMIDE DERIVATIVES USEFUL AS FUNGICIDES 审中-公开
标题翻译：作为杀菌剂有用的吡咯烷酮酸酰胺衍生物
公开(公告)号：WO2003048128A1
公开(公告)日：2003-06-12
申请号：PCT/GB2002/005303
申请日：2002-11-25
申请人： SYNGENTA LIMITED , SYNGENTA PARTICIPATIONS AG , WHITTINGHAM, William, Guy , LAWSON, Kevin, Robert , WORTHINGTON, Paul, Anthony , RUSSELL, Charles, Adam , SALMON, Roger , MAY, Leslie, Francis , JORG, Mario , PACHLATKO, Johannes, Paul
发明人： WHITTINGHAM, William, Guy , LAWSON, Kevin, Robert , WORTHINGTON, Paul, Anthony , RUSSELL, Charles, Adam , SALMON, Roger , MAY, Leslie, Francis , JORG, Mario , PACHLATKO, Johannes, Paul
IPC分类号： C07D213/65
CPC分类号： C07D213/70 , A01N43/40 , C07D213/65 , C07D213/68 , C07D213/80 , C07D213/82 , C07D213/85
摘要： Fungicidal compounds of the general formula (I): wherein X and Y are independently H, halo, C 1-8 alkyl, C 3-6 cycloalkyl, C 2-8 alkenyl, C 2-8 alkynyl, C 1-8 alkoxy, C 1-8 alkylthio, nitro, amino, mono- or di-(C 1-6 )alkylamino, mono- or di-(C 2-6 )alkenylamino, mono- or di-(C 2-6 )alkynylamino, formylamino, C 1-4 alkyl(formyl)amino, C 1-4 alkylcarbonylamino, C 1-4 alkyl(C 1-4 alkylcarbonyl)amino, cyano, formyl, C 1-4 alkylcarbonyl, C 1-4 alkoxycarbonyl, aminocarbonyl, mono- or di-(C 1-4 )alkylaminocarbonyl, carboxy, C 1-4 alkylcarbonyloxy, aryl(C 1-4 )alkylcarbonyloxy, C 1-4 alkylsulphinyl, C 1-4 alkylsulphonyl, C 1-4 alkylsulphonyloxy, aryl, heteroaryl, aryloxy, arylthio, heteroaryloxy or heteroarylthio wherein any of the foregoing alkyl, cycloalkyl, alkenyl, alkynyl, aryl, heteroaryl, groups or moieties are optionally substituted; R 1 is phenyl, cyano, C 1-4 alkyl, C 2-4 alkenyl or C 2-4 alkynyl in which the alkyl, alkenyl and alkynyl groups are optionally substituted on their terminal carbon atom with one, two or three halogen atoms, with a cyano group, with a C 1-4 alkylcarbonyl group, with a C 1-4 alkoxycarbonyl group or with a hydroxy group, or R 1 is alkoxyalkyl, alkylthioalkyl, alkylsulphinylalkyl or alkylsulphonylalkyl in which the total number of carbon atoms is 2 or 3; R 2 is H, C 1-4 alkyl, C 1-4 alkoxymethyl or benzyloxymethyl in which the phenyl ring of the benzyl moiety is optionally substituted with C 1-4 alkoxy; R 3 and R 4 are independently H, C 1-3 alkyl, C 2-3 alkenyl or C 2-3 alkynyl provided that both are not H and that when both are other than H their combined total of carbon atoms does not exceed 4, or R 3 and R 4 join with the carbon atom to which they are attached to form a 3 or 4 membered carbocyclic ring optionally containing one O, S or N atom and optionally substituted with halo or C 1-4 alkyl; and R 5 is halo, C 1-4 alkyl or C 3-4 cycloalkyl in which the alkyl or cycloalkyl group is optionally substituted with halo, hydroxy, C 1-6 alkoxy, C 1-6 alkylthio, cyano, C 1-4 alkylcarbonyloxy, aminocarbonyloxy, mono- or di(C 1-4 )alkylaminocarbonyloxy, or tri(C 1-4 )alkylsilyloxy. The compounds and compositions containing them are especially useful for combating fungal infections of plants.
摘要翻译：通式（I）的杀真菌化合物：其中X和Y独立地为H，卤素，C 1-8烷基，C 3-6环烷基，C 2-8链烯基，C 2-8 炔基，C> 1-8 <烷氧基，C 1-8烷基硫基，硝基，氨基，单 - 或二 - （C 1-6）烷基氨基，单 - 或二 - （C 2-6）链烯基氨基，单 - 或二 - （C 2-6）炔基氨基，甲酰氨基，C 1-4烷基（甲酰基）氨基，C 1-4烷基羰基氨基，C 1-4烷基（C 1 -4 <烷基羰基）氨基，氰基，甲酰基，C 1-4烷基羰基，C 1-4烷氧基羰基，氨基羰基，一或二 - （C 1-4）烷基氨基羰基，羧基， 4 <烷基羰基氧基，芳基（C 1-4）烷基羰基氧基，C 1-4烷基亚磺酰基，C 1-4烷基磺酰基，C 1-4烷基磺酰氧基，芳基，杂芳基，芳氧基，芳硫基，杂芳氧基或杂芳硫基其中任何前述烷基，环烷基，烯基，炔基，芳基，杂芳基，基团或部分任选被取代; R 1是苯基，氰基，C 1-4烷基，C 2-4链烯基或C 2-4炔基，其中烷基，烯基和炔基在其末端碳原子上任选被一个，两个或三个卤素原子取代，具有C 1-4烷基羰基，C 1-4烷氧基羰基或羟基的氰基，或者R 1是烷基烷基或烷基磺酰基烷基，其中总碳原子数为2或3的烷氧基烷基，烷硫基烷基，烷基亚磺酰基烷基或烷基磺酰基烷基 ; R 2是H，C 1-4烷基，C 1-4烷氧基甲基或苄氧基甲基，其中苄基部分的苯环任选被C 1-4烷氧基取代; R 3和R 4独立地是H，C 1-3烷基，C 2-3烯基或C 2-3炔基，条件是两者都不是H，当两者都不是H时，它们的总碳原子数不超过 4或R 3和R 4与它们所连接的碳原子一起形成任选含有一个O，S或N原子并任选被卤素或C 1-4烷基取代的3或4元碳环 ; 羟基，C 1-6烷氧基，C 1-6烷硫基，氰基，C 1-4烷基羰基氧基，氨基羰基氧基，C 1-4烷氧基，C 1-4烷氧基，，单或二（C 1-4）烷基氨基羰基氧基或三（C 1-4）烷基甲硅烷氧基。含有它们的化合物和组合物特别可用于防治植物的真菌感染。

9. 发明申请

WO2010112826A3 QUINOLINE OR NAPHTHYRIDINE HERBICIDES 审中-公开
公开(公告)号：WO2010112826A3
公开(公告)日：2010-10-07
申请号：PCT/GB2010/000598
申请日：2010-03-29
申请人： SYNGENTA LIMITED , SALMON, Roger , MITCHELL, Glynn , MORRIS, James, Alan
发明人： SALMON, Roger , MITCHELL, Glynn , MORRIS, James, Alan
IPC分类号： C07D471/04 , A01N43/90 , A01P13/00
摘要： The present invention relates to novel herbicidal compounds of Formula (I), or an agronomically acceptable salt of said compound wherein X 1 , X 2 , R 1 , R 2 , R 3 , m and Q are as defined herein. The invention further relates to processes and intermediates for the preparation of the novel herbicidal compounds, to compositions which comprise the herbicidal compounds, and to their use for controlling weeds, in particular in crops of useful plants.

10. 发明申请

WO2004108663A1 N-ALKYNYL-2- (SUBSTITUTED ARYLOXY) ALKYLTHIOAMIDE DERIVATIVES AS FUNGICIDES 审中-公开
标题翻译： N-烷基-2-（取代的芳基）烷氧基化物衍生物作为杀真菌剂
公开(公告)号：WO2004108663A1
公开(公告)日：2004-12-16
申请号：PCT/GB2004/002294
申请日：2004-05-28
申请人： SYNGENTA LIMITED , CROWLEY, Patrick, Jelf , SALMON, Roger , SAGEOT, Olivia, Anabelle , BACON, David, Philip , LANGFORD, David, William
发明人： CROWLEY, Patrick, Jelf , SALMON, Roger , SAGEOT, Olivia, Anabelle , BACON, David, Philip , LANGFORD, David, William
IPC分类号： C07C323/22
CPC分类号： C07D215/20 , C07C317/46 , C07C323/60 , C07D213/65 , C07D213/68 , C07D217/02 , C07D231/56 , C07D239/74 , C07D261/20 , C07D271/12 , C07D277/62 , C07D277/68 , C07D277/82
摘要： Fungicidal compounds of the general formula (1), wherein Ar is a group of the formula (A), (B1), (B2) or (C), or Ar is a 5- or 6-linked group of the formula (D1) or (D2); and R 1 , R 2 , R 3 , R 4 , R 5 , n, A 1 , A 2 , A 3 , A 4 , A 5 , K a , K b , L, M, V, W, X,Y and Z have the definitions given in claim 1.
摘要翻译：通式（1）的杀真菌化合物，其中Ar为式（A），（B1），（B2）或（C）的基团，或Ar为式（D1）的5-或6-连接基团）或（D2）; 和R 1，R 2，R 3，R 4，R 5，n，A 1，A 2，A 3，A 4， 5，K a，K b，L，M，V，W，X，Y和Z具有权利要求1中给出的定义。

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