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    Quinoline compounds as fungicides or bactericides
    2.
    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

    申请人： Yoshio Kurahashi ,  Koichi Moriya ,  Haruko Sawada ,  Haruhiko Sakuma ,  Ryo Watanabe ,  Asami Ito

    发明人： Yoshio Kurahashi ,  Koichi Moriya ,  Haruko Sawada ,  Haruhiko Sakuma ,  Ryo Watanabe ,  Asami Ito

    IPC分类号： A01N43/50 ,  A01N43/56 ,  C07D401/04 ,  C07D521/00 ,  C07F7/08 ,  A01N43/42 ,  C07D215/44

    CPC分类号： C07D231/12 ,  A01N43/50 ,  A01N43/56 ,  C07D233/56 ,  C07D249/08 ,  C07D401/04 ,  C07F7/0812

    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。

    Herbicidal 1-pyridyltetrazolinones
    3.
    发明授权
    Herbicidal 1-pyridyltetrazolinones 失效
    除草剂1-吡啶基四唑啉酮

    公开(公告)号：US5710278A

    公开(公告)日：1998-01-20

    申请号：US802152

    申请日：1997-02-19

    申请人： Toshio Goto ,  Koichi Moriya ,  Fritz Maurer ,  Seishi Ito ,  Katsuaki Wada ,  Kazuhiro Ukawa ,  Ryo Watanabe ,  Asami Ito

    发明人： Toshio Goto ,  Koichi Moriya ,  Fritz Maurer ,  Seishi Ito ,  Katsuaki Wada ,  Kazuhiro Ukawa ,  Ryo Watanabe ,  Asami Ito

    IPC分类号： A01N47/38 ,  C07D401/04 ,  C07D401/14

    CPC分类号： C07D401/04 ,  A01N47/38

    摘要： Herbicidal tetrazolinone derivatives of the formula: ##STR1## in which R.sup.1 is alkyl, haloalkyl, cycloalkyl, alkenyl, haloalkenyl, alkynyl or phenyl, and R.sup.2 is alkyl, haloalkyl, cycloalkyl, alkenyl, haloalkenyl, alkynyl or phenyl, or R.sup.1 and R.sup.2 together with the nitrogen atom to which they are bonded form an optionally benzofused heterocyclic ring, which is optionally substituted by C.sub.1-4 alkyl, n is 0, 1, 2 or 3, and R.sup.3 each independently is nitro, halogen, alkyl, haloalkyl, alkylthio or phenoxy.

    摘要翻译： 式中：R 1为烷基，卤代烷基，环烷基，烯基，卤代烯基，炔基或苯基，R 2为烷基，卤代烷基，环烷基，链烯基，卤代烯基，炔基或苯基，或R 1和R 2一起形成的除草四氢唑酮衍生物 与其键合的氮原子形成任选的苯并稠合的杂环，其任选被C 1-4烷基取代，n是0,1,2或3，并且R 3各自独立地是硝基，卤素，烷基，卤代烷基，烷硫基 或苯氧基。