利索-全球专利检索

  1. 登录
  2. 注册

搜索结果

57 条记录 (耗时 0.013 秒)

    1,2-dichloro-1,2,2-trimethyl-1-phenyldisilane and method for producing the same
    42.
    发明公开
    1,2-dichloro-1,2,2-trimethyl-1-phenyldisilane and method for producing the same 失效
    1,2-二氯-1,2,2-三甲基-1-苯基硅烷和方法，用于其生产。

    公开(公告)号：EP0234412A1

    公开(公告)日：1987-09-02

    申请号：EP87101915.4

    申请日：1987-02-11

    申请人： YUKI GOSEI KOGYO CO., LTD.

    发明人： Nagai, Yoichiro ,  Watanabe, Hamao ,  Akutsu, Yoshinori

    IPC分类号： C07F7/12

    CPC分类号： C07F7/12

    摘要： This invention relates to 1,2-dichloro-1,2,2-trimethyl-1-phenyldisilane expressed by the chemical formula (II),
    Cl(CH₃)₂SiSi(CH₃)(C₆H₅)Cl.
    This invention further relates to a method for producing 1,2-dichloro-1,2,2-trimethyl-1-phenyl disilane by reacting phenyl lithium with 1,1,2-trichloro-1,2,2-trimethyldisilane expressed by the chemical formula (III),
    Cl(CH₃)₂SiSi(CH₃) Cl₂.
    This invention still further relates to a method for producing 1,2-dichloro-1,2,2-trimethyl-1-phenyl disilane by reacting 1,1,2-trichloro-1,2,2-trimethyl disilane with phenyl magnesium halide expressed by the general formula (IV), C₆H₅MgX (X = halogen atom) in the presence of a cobalt catalyst.

    METHOD FOR PRODUCING 4-(PIPERIDIN-4-YL)MORPHOLINE
    45.
    发明公开
    METHOD FOR PRODUCING 4-(PIPERIDIN-4-YL)MORPHOLINE 审中-公开

    公开(公告)号：EP3470394A1

    公开(公告)日：2019-04-17

    申请号：EP17810418.8

    申请日：2017-06-09

    申请人： Yuki Gosei Kogyo Co., Ltd.

    发明人： ISHIKAWA Hiromi ,  NAKAGAWA Kiyono ,  TAKEDA Yukiko

    IPC分类号： C07D211/58 ,  C07B61/00

    摘要： The object of the present invention is to provide a method for preparing 4-(piperidin-4-yl)morpholine, which is easy to operate. The object can be solved by a method for preparing 4-(1-benzylpiperidin-4-yl)morpholine, characterized in that 5-fold molar or more of morpholine is added to 1-benzyl-4-piperidone, and the mixture is reacted with hydrogen under 1 MPa or less in the presence of platinum catalyst or palladium catalyst.

    Method of preparing a guanosine-group compound and an intermediate thereof
    48.
    发明公开
    Method of preparing a guanosine-group compound and an intermediate thereof 有权
    一种选自鸟苷的制备化合物的方法，以及它们的中间

    公开(公告)号：EP1138775A2

    公开(公告)日：2001-10-04

    申请号：EP01106745.1

    申请日：2001-03-17

    申请人： YUKI GOSEI KOGYO CO., LTD.

    发明人： Mikami, Yoichi ,  Matsumoto, Seiichiro ,  Hayashi, Yoshinori ,  Sato, Toyoki

    IPC分类号： C12P19/40

    CPC分类号： C12P19/40

    摘要： A glyoxal-guanosine-group compound is prepared either by reacting glyoxal-guanine with any one of ribose-1-phosphate and 2-deoxyribose-1-phosphate in the presence of purine nucleoside phosphorylase, or by reacting glyoxal-guanine with any one selected from the group consisting of uridine, 2'-deoxyuridine and thymidine, together with phosphate ion, in the presence of purine nucleoside phosphorylase and pyrimidine nucleoside phosphorylase. The glyoxal-guanosine-group compound is then decomposed by alkali, whereby a guanosine-group compound consisting of guanosine and 2'-deoxyguanosine is prepared.

    摘要翻译： 乙二醛 - 鸟苷类化合物是通过使乙二醛 - 鸟嘌呤与选定的核糖-1-磷酸中的任何一个和2-脱氧核糖-1-磷酸酯在嘌呤核苷磷酸化酶的存在下，或通过使乙二醛 - 鸟嘌呤与任何一种制备任一 选自尿苷，2'-脱氧尿苷和胸苷的，与磷酸根离子一起，在嘌呤核苷磷酸化酶和嘧啶核苷磷酸化酶的存在。 的乙二醛 - 鸟苷类化合物，然后通过碱，由此由......组成鸟苷和2'-脱氧鸟苷的鸟苷类化合物制备分解。