Nitro-substituted heterocyclic compounds
    82.
    发明授权
    Nitro-substituted heterocyclic compounds 失效
    硝基取代的杂环化合物

    公开(公告)号:US5622956A

    公开(公告)日:1997-04-22

    申请号:US461903

    申请日:1995-06-05

    摘要: Nitro-substituted heterocyclic compounds of the formula (I) ##STR1## wherein R is hydrogen or alkyl,Z is an optionally substituted aryl or optionally substituted heterocyclic group containing at least one atom selected from N, O and S,A is optionally substituted ethylene or optionally substituted trimethylene, andB stands for 2 or 3 members of a heterocyclic ring which is formed, together with the adjacent C-atom and N-atom and at least one of said members may represent a hetero atom and may be optionally substituted, provided that when B stands for 3 members, two of which are carbon atoms and the other one is a nitrogen atom which is located in the middle of the three members, then at least one of said two carbon atoms must be substituted by a keto group. Such compounds being useful as insecticides.

    摘要翻译: 式(I)的硝基取代的杂环化合物其中R是氢或烷基,Z是任选取代的芳基或含有至少一个选自N,O和S的原子的任选取代的杂环基,A是 任选取代的乙烯或任选取代的三亚甲基,B代表与相邻C原子和N-原子一起形成的杂环的2或3个成员,并且所述成员中的至少一个可以表示杂原子,并且可以是 任选取代,条件是当B代表3个成员时,其中两个是碳原子,另一个是位于三个成员中间的氮原子,则所述两个碳原子中的至少一个必须被 一个酮基。 这些化合物可用作杀虫剂。

    Quinoline compounds as fungicides or bactericides
    83.
    发明授权
    Quinoline compounds as fungicides or bactericides 失效
    喹啉化合物作为杀真菌剂或杀菌剂

    公开(公告)号:US5622914A

    公开(公告)日:1997-04-22

    申请号:US529963

    申请日:1995-09-19

    摘要: Combatting fungi and bacteria with quinoline derivatives of the formula ##STR1## in which X is a nitrogen atom and Y is a CH-group orY is a nitrogen atom and X is a CH-group,R is hydrogen, halogen, acetyl or alkyl which is optionally substituted by one to three radicals independently selected from the group consisting of alkoxy, phenyl, hydroxy, halogen and cyano, orR is alkenyl which is optionally substituted by one to three radicals independently selected from the group consisting of halogen, cyano, alkoxy, phenyl and hydroxy, orR is alkynyl which is optionally substituted by one to three radicals independently selected from the group consisting of halogen, phenyl, trimethylsilyl, hydroxy, cyano, alkoxy, alkylamino, dialkylamino, alkylcarbonyl, tolyl, alkoxycarbonyl and alkylcarbonyloxy, orR is cycloalkyl which is optionally substituted by one to three radicals independently selected from the group consisting of halogen and cyano,A is hydrogen or halogen andB is halogen or halogenoalkyl,or an acid addition salt or metal salt complex thereof, and processes for their preparation. Most of these compounds are new.

    摘要翻译: 用真菌和细菌与其中X是氮原子并且Y是CH-基团或Y是氮原子并且X是CH-基团的式(I)的喹啉衍生物反应,R是氢,卤素, 乙酰基或烷基,其任选地被一至三个独立地选自烷氧基,苯基,羟基,卤素和氰基的基团取代,或R是任选被一至三个独立地选自卤素 氰基,烷氧基,苯基和羟基,或R是任选被一至三个独立地选自卤素,苯基,三甲基甲硅烷基,羟基,氰基,烷氧基,烷基氨基,二烷基氨基,烷基羰基,甲苯基,烷氧基羰基 和烷基羰基氧基,或R是任选被一至三个独立地选自卤素和氰基的基团取代的环烷基,A是氢或卤素,B是卤素或 卤代烷基或其酸加成盐或金属盐络合物,及其制备方法。 这些化合物大部分是新的。