Novel HMG-COA reductase inhibitors
    3.
    发明公开
    Novel HMG-COA reductase inhibitors 失效
    的HMG-CoA-Reduktase,缝边。

    公开(公告)号:EP0325817A1

    公开(公告)日:1989-08-02

    申请号:EP88203032.3

    申请日:1988-12-29

    申请人: Merck & Co., Inc.

    CPC分类号: C07D309/30

    摘要: Novel 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors are useful as antihypercholesterolemic agents and are represented by the following general structural formulae (I) and (II):

    摘要翻译: 新型3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)还原酶抑制剂可用作抗高血胆固醇血症药,并由以下一般结构式(I)和(II)表示: r

    Substituted biphenyl-2-carboxaldehydes and a process for preparing them
    10.
    发明公开
    Substituted biphenyl-2-carboxaldehydes and a process for preparing them 失效
    取代基联苯-2-甲醛和Verfahren zu ihrer Herstellung。

    公开(公告)号:EP0038061A1

    公开(公告)日:1981-10-21

    申请号:EP81102810.9

    申请日:1981-04-13

    申请人: Merck & Co., Inc.

    摘要: Substituted biphenyl-2-carboxaldehydes are prepared in good yield by reacting palladium complexes of substituted benzaldehyde aniline Schiff bases with substituted phenylmagnesium bromides in the presence of at least six, preferably eight, molar equivalents of triphenylphosphine. Those compounds are intermediates for synthetic, in vivo cholesterol synthesis inhibitors.

    摘要翻译: 通过使取代的苯甲醛苯胺席夫碱的钯络合物与取代的苯基溴化镁在至少6个,优选8摩尔当量的三苯基膦存在下反应,以良好的产率制备取代的联苯-2-甲醛。 那些化合物是合成的体内胆固醇合成抑制剂的中间体。