Fungicidal oximes and hydrazones
    3.
    发明授权
    Fungicidal oximes and hydrazones 失效
    杀真菌肟和腙

    公开(公告)号:US08722678B2

    公开(公告)日:2014-05-13

    申请号:US13640092

    申请日:2011-04-15

    摘要: Disclosed are compounds of Formula 1, including all stereoisomers, N-oxides, and salts thereof, wherein E, X, G, W2 and Z are as defined in the disclosure. Also disclosed are compositions containing the compounds of Formula 1 and methods for controlling plant disease caused by a fungal pathogen comprising applying an effective amount of a compound or a composition of the invention.Also disclosed are compounds of Formula 1A including all stereoisomers, N-oxides, and salts thereof, wherein E, X, G and Z1 are as defined in the disclosure. Also disclosed is the use of the compounds of Formula 1A as intermediates for preparing compounds of Formula 1.

    摘要翻译: 公开了式1的化合物,包括所有立体异构体,N-氧化物及其盐,其中E,X,G,W 2和Z如本公开所定义。 还公开了含有式1化合物的组合物和用于控制由真菌病原体引起的植物病害的方法,包括施用有效量的本发明化合物或组合物。 还公开了包括所有立体异构体,N-氧化物及其盐的式1A化合物,其中E,X,G和Z1如本公开所定义。 还公开了式1A化合物作为制备式1化合物的中间体的用途。

    Preparation of fungicidal quinazolinones and useful intermediates
    4.
    发明授权
    Preparation of fungicidal quinazolinones and useful intermediates 有权
    杀真菌喹唑啉酮和有用的中间体的制备

    公开(公告)号:US6166208A

    公开(公告)日:2000-12-26

    申请号:US202394

    申请日:1998-12-09

    摘要: This invention provides advantageous processes for preparing quinazolinones of Formula I ##STR1## wherein: R.sup.1 is C.sub.1 -C.sub.10 alkyl; C.sub.3 -C.sub.10 alkenyl; C.sub.3 -C.sub.10 cycloalkyl; C.sub.3 -C.sub.10 halocycloalkyl; C.sub.4 -C.sub.10 cycloalkylalkyl; C.sub.4 -C.sub.10 halocycloalkylalkyl; or C.sub.3 -C.sub.10 alkynyl;R.sup.2 is C.sub.1 -C.sub.10 alkyl; C.sub.3 -C.sub.10 alkenyl; C.sub.3 -C.sub.10 cycloalkyl; C.sub.3 -C.sub.10 halocycloalkyl; C.sub.4 -C.sub.10 cycloalkylalkyl; C.sub.4 -C.sub.10 halocycloalkylalkyl; C.sub.4 -C.sub.10 cycloalkyl; C.sub.4 -C.sub.10 halocycloalkyl; or C.sub.3 -C.sub.10 alkynyl; andR.sup.3 and R.sup.4 are each independently hydrogen or halogen; from compounds containing the moiety IIg ##STR2## This invention further provides certain compounds of Formula II, IIIa, or IVa ##STR3## where R.sup.7 is C.sub.2 -C.sub.6 alkyl.

    摘要翻译: PCT No.PCT / US97 / 10254 Sec。 371 1998年12月9日第 102(e)日期1998年12月9日PCT提交1997年6月12日PCT公布。 公开号WO97 / 48684 日期1997年12月24日本发明提供了制备式I的喹唑啉酮的有利方法,其中:R1是C1-C10烷基; C 3 -C 10烯基; C3-C10环烷基; C 3 -C 10卤代环烷基; C4-C10环烷基烷基; C 4 -C 10卤代环烷基烷基; 或C 3 -C 10炔基; R2是C1-C10烷基; C 3 -C 10烯基; C3-C10环烷基; C 3 -C 10卤代环烷基; C4-C10环烷基烷基; C 4 -C 10卤代环烷基烷基; C4-C10环烷基; C 4 -C 10卤代环烷基; 或C 3 -C 10炔基; 且R 3和R 4各自独立地为氢或卤素; 含有部分IIg的化合物本发明进一步提供某些其中R 7为C 2 -C 6烷基的式II,IIIa或IVa化合物。