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1. 发明授权

US4308209A .beta.-Lactones of 2-hydroxy-cyclopentane-carboxylic acids 失效
标题翻译： β-内酯2-羟基 - 环戊烷 - 羧酸的内酯
公开(公告)号：US4308209A
公开(公告)日：1981-12-29
申请号：US216124
申请日：1980-12-15
申请人： Jean Buendia , Michel Vivat , Laurent Taliani
发明人： Jean Buendia , Michel Vivat , Laurent Taliani
IPC分类号： A61K31/337 , A61K31/34 , A61K31/365 , A61K31/38 , A61P9/12 , C07D305/14 , C07D309/12 , C07D333/32 , C07D409/06 , C07D409/12
CPC分类号： C07D333/32 , C07D305/14 , C07D309/12
摘要： Novel .beta.-lactones of 2-hydroxy-cyclopentane-carboxylic acids of the formula ##STR1## wherein R.sub.1 is selected from the group consisting of hydrogen and methyl and R.sub.2 is selected from the group consisting of --CH.sub.2 --O--CH.sub.2 --CH.sub.3 and --X--Ar, X is selected from the group consisting of --O-- and --CH.sub.2 --, Ar is an optionally substituted member selected from the group consisting of thienyl, thiazolyl, phenyl and thiadiazolyl, the optional substituents being at least one member selected from the group consisting of halogen and --CF.sub.3 and the wavy lines indicate that the groups may be in the .alpha.,.beta. or .beta.,.alpha.-positions or mixtures thereof having hypotensive activity and their preparation.
摘要翻译：式（I）的2-羟基 - 环戊烷 - 羧酸的新型β-内酯，其中R 1选自氢和甲基，R 2选自-CH 2 -O-CH 2 -CH 3和 -X-Ar，X选自-O-和-CH 2 - ，Ar是选自噻吩基，噻唑基，苯基和噻二唑基的任选取代的成员，任选的取代基是至少一个选自由卤素和-CF 3组成的组和波浪线表示这些基团可以是具有低血压活性的α，β或β，α-位或其混合物及其制备。

2. 发明授权

US4264623A .beta.-Lactones of 2-hydroxy-cyclopentane-carboxylic acids 失效
标题翻译： β-内酯2-羟基 - 环戊烷 - 羧酸的内酯
公开(公告)号：US4264623A
公开(公告)日：1981-04-28
申请号：US94771
申请日：1979-11-16
申请人： Jean Buendia , Michel Vivat , Laurent Taliani
发明人： Jean Buendia , Michel Vivat , Laurent Taliani
IPC分类号： A61K31/337 , A61K31/34 , A61K31/365 , A61K31/38 , A61P9/12 , C07D305/14 , C07D309/12 , C07D333/32 , C07D409/06 , C07D409/12 , C09B23/16 , C09B23/08
CPC分类号： C07D333/32 , C07D305/14 , C07D309/12
摘要： Novel .beta.-lactones of 2-hydroxy-cyclopentane-carboxylic acids of the formula ##STR1## wherein R.sub.1 is selected from the group consisting of hydrogen and methyl and R.sub.2 is selected from the group consisting of --CH.sub.2 --O--CH.sub.2 --CH.sub.3 and --X--Ar, X is selected from the group consisting of --O-- and --CH.sub.2 --, Ar is an optionally substituted member selected from the group consisting of thienyl, thiazolyl, phenyl and thiadiazolyl, the optional substituents being at least one member selected from the group consisting of halogen and --CF.sub.3 and thw wavy lines indicate that the groups may be in the .alpha., .beta. or .beta., .alpha.-positions or mixtures thereof having hypotensive activity and their preparation.
摘要翻译：式（I）的2-羟基 - 环戊烷 - 羧酸的新型β-内酯，其中R 1选自氢和甲基，R 2选自-CH 2 -O-CH 2 -CH 3和 -X-Ar，X选自-O-和-CH 2 - ，Ar是选自噻吩基，噻唑基，苯基和噻二唑基的任选取代的成员，任选的取代基是至少一个选自由卤素和-CF 3和波浪线组成的组表示这些基团可以是具有降血压活性的α，β或β，α-位或其混合物及其制备。

3. 发明授权

US4155996A 3-(Phosphoryloxy) and (phosphonyloxy)-thiophenes 失效
标题翻译： 3-（磷酰氧基）和（膦酰氧基） - 噻吩
公开(公告)号：US4155996A
公开(公告)日：1979-05-22
申请号：US944809
申请日：1978-09-22
申请人： Jacques Perronnet , Laurent Taliani
发明人： Jacques Perronnet , Laurent Taliani
IPC分类号： C07F9/6553 , A01N9/36 , C07F9/09 , C07F9/165
CPC分类号： C07F9/655345
摘要： Novel 3-(phosphoryloxy) or (phosphonyloxy)-thiophenes of the formula ##STR1## wherein R is alkyl of 1 to 4 carbon atoms, R.sub.1 is selected from the group consisting of alkyl of 1 to 4 carbon atoms, alkoxy of 1 to 4 carbon atoms and ##STR2## wherein R' and R" are individually selected from the group consisting of hydrogen and alkyl of 1 to 4 carbon atoms, R.sub.2 is selected from the group consisting of cyano, alkoxy carbonyl of 2 to 4 carbon atoms and ##STR3## wherein Z is selected from the group consisting of phenyl and alkyl of 1 to 4 carbon atoms, R.sub.3 is selected from the group consisting of alkyl of 1 to 6 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, phenyl, morpholino, piperidinyl and alkoxy carbonyl of 2 to 4 carbon atoms and X is selected from the group consisting of oxygen and sulfur having pesticidal properties and their preparation.
摘要翻译：新颖的3-（磷酰氧基）或（膦酰基氧基） - 噻吩类化合物其中R是1至4个碳原子的烷基，R 1选自1至4个碳原子的烷基，1至 4个碳原子和其中R'和R“分别选自氢和1至4个碳原子的烷基，R 2选自氰基，2至4个碳原子的烷氧基羰基和其中Z选自苯基和1至4个碳原子的烷基，R 3选自1至6个碳原子的烷基，1至6个碳原子的烷氧基，1至6个碳原子的烷硫基， 2个碳原子的苯基，吗啉代，哌啶基和烷氧基羰基，X选自具有杀虫特性的氧和硫及其制备。

4. 发明授权

US4128562A Novel 3-(phosphoryloxy) and (phosphonyloxy)-thiophenes 失效
标题翻译：新的3-（磷酰氧基）和（膦酰氧基） - 噻吩
公开(公告)号：US4128562A
公开(公告)日：1978-12-05
申请号：US850922
申请日：1977-11-14
申请人： Jacques Perronnet , Laurent Taliani
发明人： Jacques Perronnet , Laurent Taliani
IPC分类号： C07F9/6553 , C07D333/16 , A01N9/36 , C07D333/00
CPC分类号： C07F9/655345
摘要： Novel 3-(phosphoryloxy) or (phosphonyloxy)-thiophenes of the formula ##STR1## wherein R is alkyl of 1 to 4 carbon atoms, R.sub.1 is selected from the group consisting of alkyl of 1 to 4 carbon atoms, alkoxy of 1 to 4 carbon atoms and ##STR2## wherein R' and R" are individually selected from the group consisting of hydrogen and alkyl of 1 to 4 carbon atoms, R.sub.2 is selected from the group consisting of cyano, alkoxy carbonyl of 2 to 4 carbon atoms and ##STR3## wherein Z is selected from the group consisting of phenyl and alkyl of 1 to 4 carbon atoms, R.sub.3 is selected from the group consisting of alkyl of 1 to 6 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, phenyl, morpholino, piperidinyl and alkoxy carbonyl of 2 to 4 carbon atoms and X is selected from the group consisting of oxygen and sulfur having pesticidal properties and their preparation.
摘要翻译：新颖的3-（磷酰氧基）或（膦酰基氧基） - 噻吩类化合物其中R是1至4个碳原子的烷基，R 1选自1至4个碳原子的烷基，1至 4个碳原子和其中R'和R“分别选自氢和1至4个碳原子的烷基，R 2选自氰基，2至4个碳原子的烷氧基羰基和其中Z选自苯基和1至4个碳原子的烷基，R 3选自1至6个碳原子的烷基，1至6个碳原子的烷氧基，1至6个碳原子的烷硫基， 2个碳原子的苯基，吗啉代，哌啶基和烷氧基羰基，X选自具有杀虫特性的氧和硫及其制备。

5. 发明授权

US4020076A Novel phosphoryloxy-thiazoles 失效
标题翻译：新型磷酰氧基 - 噻唑
公开(公告)号：US4020076A
公开(公告)日：1977-04-26
申请号：US611710
申请日：1975-09-09
申请人： Jacques Perronnet , Laurent Taliani
发明人： Jacques Perronnet , Laurent Taliani
IPC分类号： A01N57/16 , A01N57/08 , A01N57/24 , C07D277/56 , C07F9/6539
CPC分类号： C07F9/6539 , A01N57/08
摘要： Novel 4-phosphoryloxy-5-cyano-thiazoles of the formula ##STR1## wherein R is selected from the group consisting of alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, cycloalkyl of 3 to 8 carbon atoms and benzyl optionally substituted with 1 to 2 members of the group consisting of halogen,methyl and methoxy, R.sub.1 is selected from the group consisting of alkyl and alkoxy of 1 to 3 carbon atoms, R.sub.2 is alkyl of 1 to 3 carbon atoms and X and Z are individually selected from the group consisting of oxygen and sulfur having particularly insecticidal properties but also acaricidal and nematocidal properties.
摘要翻译：具有下式的新型4-磷酰氧基-5-氰基 - 噻唑：其中R选自1至6个碳原子的烷基，2至6个碳原子的烯基，3至8个碳原子的环烷基和任选被1至2个由卤素，甲基和甲氧基组成的基团取代的苄基，R 1选自1至3个碳原子的烷基和烷氧基，R 2是1至3个碳原子的烷基，X和Z 分别选自具有特别杀虫性能的氧和硫的组合，但也是杀螨和杀线虫性质。

6. 发明授权

US3948925A Novel thiazole derivatives 失效
标题翻译：新型噻唑衍生物
公开(公告)号：US3948925A
公开(公告)日：1976-04-06
申请号：US515479
申请日：1974-10-17
申请人： Jacques Perronnet , Laurent Taliani
发明人： Jacques Perronnet , Laurent Taliani
IPC分类号： A01N57/08 , A01N57/16 , A01P7/02 , A01P7/04 , C07D277/34 , C07D277/56 , C07F9/6539
CPC分类号： C07F9/6539 , C07D277/34 , C07D277/56
摘要： Novel compounds of the formula ##EQU1## wherein X is selected from the group consisting of oxygen and sulfur, X.sub.1 is selected from the group consisting of alkyl of 1 to 6 carbon atoms, cyano and ##EQU2## Y.sub.1 is selected from the group consisting of alkyl of 1 to 6 carbon atoms, alkoxy of 1 to 6 carbon atoms and amino, n is 0, 1 or 2, X.sub.2 is selected from the group consisting of hydrogen, chlorine, bromine, alkyl of 1 to 6 carbon atoms, cyano and ##EQU3## R is alkyl of 1 to 6 carbon atoms, R.sub.1 is selected from the group consisting of alkyl of 1 to 6 carbon atoms, alkoxy of 1 to 6 carbon atoms and ##EQU4## and R.sub.2 and R.sub.3 are selected from the group consisting of hydrogen and alkyl of 1 to 6 carbon atoms with the proviso that X.sub.1 is other than alkyl when X.sub.2 is alkyl or hydrogen, having insecticidal, nematocidal and acaricidal properties.
摘要翻译：新的式X 1化合物：其中X选自氧和硫，X 1选自由以下组成的组：1〜（CH 2）n C-Y 1，Y 1选自1至6个碳原子的烷基，1至6个碳原子的烷氧基和氨基，n是0,1或2， X 2选自氢，氯，溴，1至6个碳原子的烷基，氰基和O平行 - （CH 2）n C-Y 1，R是1至6个碳原子的烷基，R 1选自由1至6个碳原子的烷基，1至6个碳原子的烷氧基和R2-ANGLE R3组成的组，R2和R3选自氢和1至6个碳原子的烷基，条件是X1是其他当X2是烷基或氢时，具有烷基，具有杀虫，杀线虫和杀螨性质。

7. 发明授权

US4798901A Novel pyrrole derivatives 失效
标题翻译：新型吡咯衍生物
公开(公告)号：US4798901A
公开(公告)日：1989-01-17
申请号：US127922
申请日：1987-12-02
申请人： Jean Tessier , Jean-Pierre Demoute , Laurent Taliani
发明人： Jean Tessier , Jean-Pierre Demoute , Laurent Taliani
IPC分类号： A01N43/36 , A01N53/00 , A01N53/04 , A01N53/06 , A23K1/16 , C07D207/32 , C07D207/333 , C07D207/337 , C07D207/34 , C07D207/42 , C07D207/325
CPC分类号： C07D207/333 , A01N43/36 , A01N53/00 , A23K20/132 , C07D207/337 , C07D207/34 , C07D207/42
摘要： Novel pyrrole derivatives of the formula ##STR1## wherein one of R.sub.2 and R.sub.3 is ##STR2## and the other of R.sub.2 and R.sub.3 as well as R.sub.4 and R.sub.5 are individually selected from the group consisting of hydrogen, halogen, alkyl of 1 to 18 carbon atoms, aryl of 6 to 14 carbon atoms, aralkyl of 7 to 18 carbon atoms, --CN, --CF.sub.3, --NO.sub.2, --COOAlk and Alk is alkyl of 1 to 8 carbon atoms, alkoxy of 1 to 8 carbon atoms, ##STR3## n is 0, 1 or 2, R', R.sub.1 ' and R.sub.2 ' are alkyl of 1 to 8 carbon atoms and R.sub.4 and R.sub.5 taken together with the carbon atoms to which they are attached may form an optionally further unsaturated carbon homocycle of up to 8 carbon atoms, Z is selected from the group consisting of hydrogen, --CN, --C.tbd.CH, --CF.sub.3 and alkyl of 1 to 3 carbon atoms, A is the residue of a pyrethrinoid acid, R.sub.1 is selected from the group consisting of ##STR4## X', X, Y, Y' and Y" are individually selected from the group consisting of hydrogen, halogen, alkyl of 1 to 8 carbon atoms and aryl of 6 to 14 carbon atoms, the dotted line indicating an optional double bond, r' is selected from the group consisting of hydrogen, alkyl of 1 to 18 carbon atoms, aryl of 6 to 14 carbon atoms, aralkyl of 7 to 18 carbon atoms, --CF.sub.3, --COOAlk and alkoxy of 1 to 8 carbon atoms and Alk has the above definition, R" and R"' are individually selected from the group consisting of hydrogen, alkyl of 1 to 8 carbon atoms, aryl of 6 to 14 carbon atoms, aralkyl of 6 to 18 carbon atoms, --CF.sub.3, --COOAlk' and alkoxy of 1 to 8 carbon atoms and Alk' is alkyl of 1 to 8 carbon atoms having pesticidal properties and novel intermediates.
摘要翻译：式（I）的新颖的吡咯衍生物，其中R 2和R 3之一是R 1和R 2之一，以及R 4和R 5中的另一个分别选自氢，卤素，1至18的烷基碳原子数为6〜14的芳基，碳原子数为7〜18的芳烷基，-CN，-CF 3，-NO 2，-COOAlk，Alk为碳原子数为1〜8的烷基，碳原子数为1〜8的烷氧基，图像> n是0,1或2，R'，R 1'和R 2'是1至8个碳原子的烷基，R 4和R 5与它们所连接的碳原子一起可以形成任选的另外的不饱和碳均质碳 Z最多为8个碳原子，Z选自氢，-CN，-C3BCH，-CF3和1至3个碳原子的烷基，A是除虫烯酸的残基，R1选自由X，Y，Y'分别选自氢，卤素，碳原子数1〜8的烷基，碳原子数为6〜14的芳基组成的组合 n个原子，表示任选的双键的虚线，r'选自氢，1至18个碳原子的烷基，6至14个碳原子的芳基，7至18个碳原子的芳烷基，-CF 3， -COOAlk和1-8个碳原子的烷氧基，Alk具有上述定义，R“和R”'分别选自氢，1至8个碳原子的烷基，6至14个碳原子的芳基 6〜18个碳原子的芳烷基，-CF 3，-COOAlk'和1〜8个碳原子的烷氧基，Alk'是具有杀虫性的1〜8个碳原子的烷基和新的中间体。

8. 发明授权

US4737513A Novel pyrrole derivatives 失效
标题翻译：新型吡咯衍生物
公开(公告)号：US4737513A
公开(公告)日：1988-04-12
申请号：US765317
申请日：1985-08-13
申请人： Jean Tessier , Jean-Pierre Demoute , Laurent Taliani
发明人： Jean Tessier , Jean-Pierre Demoute , Laurent Taliani
IPC分类号： A01N43/36 , A01N53/00 , A01N53/04 , A01N53/06 , A23K1/16 , C07D207/32 , C07D207/333 , C07D207/337 , C07D207/34 , C07D207/42 , A61K31/40 , C07D207/325
CPC分类号： C07D207/333 , A01N43/36 , A01N53/00 , A23K20/132 , C07D207/337 , C07D207/34 , C07D207/42
摘要： Novel pyrrole derivatives of the formula ##STR1## wherein one of R.sub.2 and R.sub.3 is ##STR2## and the other of R.sub.2 and R.sub.3 as well as R.sub.4 and R.sub.5 are individually selected from the group consisting of hydrogen, halogen, alkyl of 1 to 18 carbon atoms, aryl of 6 to 14 carbon atoms, aralkyl of 7 to 18 carbon atoms, --CN, --CF.sub.3, --NO.sub.2, --COOAlk and Alk is alkyl of 1 to 8 carbon atoms, alkoxy of 1 to 8 carbon atoms, ##STR3## n is 0, 1 or 2, R', R.sub.1 ' and R.sub.2 ' are alkyl of 1 to 8 carbon atoms and R.sub.4 and R.sub.5 taken together with the carbon atoms to which they are attached may form an optionally further unsaturated carbon homocycle of up to 8 carbon atoms, Z is selected from the group consisting of hydrogen, --CN, --C.tbd.CH, --CF.sub.3 and alkyl of 1 to 3 carbon atoms, A is the residue of a pyrethrinoid acid, R.sub.1 is selected from the group consisting of ##STR4## X', X, Y, Y' and Y" are individually selected from the group consisting of hydrogen, halogen, alkyl of 1 to 8 carbon atoms and aryl of 6 to 14 carbon atoms, the dotted line indicating an optional double bond, r' is selected from the group consisting of hydrogen, alkyl of 1 to 18 carbon atoms, aryl of 6 to 14 carbon atoms, aralkyl of 7 to 18 carbon atoms, --CF.sub.3, --COOAlk and alkoxy of 1 to 8 carbon atoms and Alk has the above definition, R" and R'" are individually selected from the group consisting of hydrogen, alkyl of 1 to 8 carbon atoms, aryl of 6 to 14 carbon atoms, aralkyl of 6 to 18 carbon atoms, --CF.sub.3 ' --COOAlk' and alkoxy of 1 to 8 carbon atoms and Alk' is alkyl of 1 to 8 carbon atoms having pesticidal properties and novel intermediates.
摘要翻译：式（I）的新颖的吡咯衍生物，其中R 2和R 3之一是R 1和R 2之一，以及R 4和R 5中的另一个分别选自氢，卤素，1至18的烷基碳原子数为6〜14的芳基，碳原子数为7〜18的芳烷基，-CN，-CF 3，-NO 2，-COOAlk，Alk为碳原子数为1〜8的烷基，碳原子数为1〜8的烷氧基，图像> n是0,1或2，R'，R 1'和R 2'是1至8个碳原子的烷基，R 4和R 5与它们所连接的碳原子一起可以形成任选的另外的不饱和碳均质碳 Z最多为8个碳原子，Z选自氢，-CN，-C3BCH，-CF3和1至3个碳原子的烷基，A是除虫烯酸的残基，R1选自由X，Y，Y'分别选自氢，卤素，碳原子数为1〜8的烷基，碳原子数为6〜14的芳基，表示任选的双键的虚线，r'选自氢，1至18个碳原子的烷基，6至14个碳原子的芳基，7至18个碳原子的芳烷基，-CF 3，-COOAlk和烷氧基 1〜8个碳原子，Alk具有上述定义，R“和R”'分别选自氢，1〜8个碳原子的烷基，6〜14个碳原子的芳基，6个芳烷基至18个碳原子，-CF 3'-COOAlk'和1至8个碳原子的烷氧基，Alk'是具有杀虫特性的1至8个碳原子的烷基和新的中间体。

9. 发明授权

US3932433A Pesticidal phosphorous-thiazole compounds 失效
标题翻译：杀虫磷 - 噻唑化合物
公开(公告)号：US3932433A
公开(公告)日：1976-01-13
申请号：US536424
申请日：1974-12-26
申请人： Jacques Perronnet , Laurent Taliani
发明人： Jacques Perronnet , Laurent Taliani
IPC分类号： A01N57/16 , A01P7/02 , A01P7/04 , C07F9/6539 , C07F9/6541 , C07D277/60
CPC分类号： C07F9/6541 , A01N57/16
摘要： Thiazole derivatives of the formula ##SPC1##Wherein A is alkylene of 3 to 5 carbon atoms optionally substituted with a member of the group consisting of =0 and ##EQU1## wherein R' is alkyl of 1 to 5 carbon atoms and R is alkyl of 2 to 3 carbon atoms having insecticidal and/or acaricidal properties and their preparation.
摘要翻译：式WHEREIN A的噻唑衍生物是任选被0和O并原-C-OR'的成员任意取代的3至5个碳原子的亚烷基，其中R'是1至5个碳原子的烷基，R是烷基具有2至3个具有杀虫和/或杀螨性质的碳原子及其制备。

10. 发明授权

US5064861A Acylated amine compounds which are useful fungicigal agents 失效
标题翻译：有用的真菌药剂的胺化合物
公开(公告)号：US5064861A
公开(公告)日：1991-11-12
申请号：US454685
申请日：1989-12-21
申请人： Jean-Louis Brayer , Laurent Taliani , Jean Tessier
发明人： Jean-Louis Brayer , Laurent Taliani , Jean Tessier
IPC分类号： A01N37/18 , A01N37/20 , A01N39/04 , A01N43/16 , A01N43/38 , A01N47/44 , C07C53/21 , C07C57/72 , C07C59/70 , C07C233/39 , C07C235/20 , C07C279/12 , C07C279/24 , C07D209/08 , C07D209/10 , C07D209/12 , C07D311/16
CPC分类号： C07D209/08 , A01N37/20 , A01N39/04 , A01N43/16 , A01N43/38 , A01N47/44 , C07C233/39 , C07C235/20 , C07C279/12 , C07C53/21 , C07C57/72 , C07C59/70 , C07D209/10 , C07D209/12 , C07D311/16
摘要： A compound selected from the group consisting of a compound of the formula ##STR1## wherein R.sub.1 is selected from the group consisting of Ar-O- and aryl, polyaryl and condensed polyaryl unsubstituted or substituted and heterocycle unsubstituted or substituted, Ar is aryl of 6 to 14 carbon atoms unsubstituted or substituted, heteroaryl unsubstituted or substituted and heterocyclic unsubstituted or substituted, W is selected from the group comsisting of --(CH.sub.2).sub.n.sbsb.1 --or --(CH.sub.2).sub.n.sbsb.2 --NY--(CH.sub.2).sub.n.sbsb.3, n.sub.1, n.sub.2 and n.sub.3 are individually integers from 2 to 6, Y is selected from the group consisting of hydrogen, alkyl of 1 to 12 carbon atoms, aryl of 6 to 12 carbon atoms and aralkyl of 7 to 14 carbon atoms unsubstituted or substituted, --COOAlk and --COR.sub.2, Alk is alkyl of 1 to 12 carbon atoms, R.sub.2 is selected from the group consisting of alkyl of 1 to 12 carbon atoms, alkenyl and alkynyl of 2 to 12 carbon atoms, aryl of 6 to 14 carbon atoms, aralkyl of 7 to 18 carbon atoms unsubstituted or substituted and heterocyclic unsubstituted or substituted, Z is selected from the group consisting of hydrogen, ##STR2## R.sub.2 is alkyl of 1 to 12 carbon atoms or aralkyl of 7 to 18 carbon atoms, Alk' is alkyl of 1 to 12 carbon atoms, ArAlk is aralkyl of 7 to 18 carbon atoms, R.sub.2 ' is R.sub.2, R.sub.3 and R.sub.3 ' are selected from the group consisting of aryl substituted or unsubstituted, heteroaryl substituted or unsubstituted, heterocyclic unsubstituted or substituted and R.sub.1 with the proviso that Z is not hydrogen when W is --(CH.sub.2).sub.3 --and R.sub.1 is 2,4-dichlorophenoxy and their non-toxic, pharmaceutically acceptable acid addition salts having fungicidal activity.
摘要翻译：选自下式的化合物的化合物其中R 1选自Ar-O-和芳基，聚芳基和未取代或取代的缩合聚芳基，未取代或取代的杂环，Ar是未取代或未取代的未取代或未取代的杂芳基，未取代或取代的杂芳基，W选自 - （CH 2）n1 - 或 - （CH 2）n 2 -YH-（CH 2）n3，n1，n2 和n3各自为2至6的整数，Y选自氢，1至12个碳原子的烷基，6至12个碳原子的芳基和未被取代或取代的7-14个碳原子的芳烷基，-COOAlk和 -COR 2，Alk为1〜12个碳原子的烷基，R2选自1〜12个碳原子的烷基，2〜12个碳原子的烯基和炔基，6〜14个碳原子的芳基，7个芳烷基至18个碳原子未被取代或取代和杂合 Z取代或未取代的Z选自氢，-COCH 2 R 3，R 2是1至12个碳原子的烷基或7至18个碳原子的芳烷基，Alk'是1至12个碳的烷基原子，ArAlk是7至18个碳原子的芳烷基，R2'是R2，R3和R3'选自芳基取代或未取代的杂芳基取代或未取代的杂环，未取代或取代的杂环，R1是条件是Z是当W是 - （CH 2）3 - 且R 1是2,4-二氯苯氧基时，它们不是氢，它们是具有杀真菌活性的无毒的药学上可接受的酸加成盐。

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