高等学校化学学报 ›› 1999, Vol. 20 ›› Issue (5): 736.

• 论文 • 上一篇    下一篇

MK-287类PAF拮抗剂的合成

林辉1, 史鸿鑫2, MandvillG.3   

  1. 1. 浙江大学湖滨校区机能中心, 杭州 310006;
    2. 浙江工业大学化工学院, 杭州 310014;
    3. Lab.des Carbocycles, I.C.M.O.Universite de Paris-Sud, 91405, Orsay Cedex, France
  • 出版日期:1999-05-24 发布日期:1999-05-24
  • 通讯作者: 林 辉,女,40岁,实验师.
  • 作者简介:林 辉,女,40岁,实验师.
  • 基金资助:

    中法政府科技合作项目;浙江省科学技术委员会资助

Synthesis of Some Antagonists of PAF of MK 287's Kind

LIN Hui1, SHI Hong-Xin2, MandvillG.3   

  1. 1. Central Laboratory of Biochemistry & Physiological Sciences, Hubin Campus, Zhejiang University, Hangzhou, 310006;
    2. College of Chemical Engineering, Zhejiang University of Technology, Hangzhou, 310014;
    3. Lab.des Carbocycles, I.C.M.O.Universite de Paris-Sud, 91405, Orsay Cedex, France
  • Online:1999-05-24 Published:1999-05-24

摘要: 以(±)-4,10-二氧杂三环[5,2,1,02,6]-癸-8-烯-3-醇和PhTi(OPr-i)3为原料,经过芳基化、氧化、芳基化、环化、热分解和加氢反应,高立体选择性地合成了反式-2,5-二芳基四氢呋喃.

关键词: 合成, 立体选择性, 手性, 二芳基四氢呋喃

Abstract: Trans 2,5-diaryltetrahydrofuran is a potent antagonist of platelet activating factor. It is obtained in high stereoselectivity by the reactions of arylation, oxidation, arylation, cyclization, hot decomposition and hydrogenation starting from (±)4,10-dioxatricyclo[5,2,1,02,6]-dec-8-ene-3-ole and PhTi(OPr-i)3.

Key words: Synthesis, Stereoselectivity, Chiral, Diaryltetrahydrofuran

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