有机化学 ›› 2006, Vol. 26 ›› Issue (9): 1208-1216. 上一篇    下一篇

综述与进展

手性催化的环氧化物立体选择性开环反应

王磊a,b,李叶芝a,黄化民a,方唯硕*,b   

  1. (a吉林大学化学学院 长春 130023)
    (b中国医学科学院中国协和医科大学药物研究所 北京 100050)
  • 收稿日期:2005-03-29 修回日期:1900-01-01 发布日期:2006-09-11
  • 通讯作者: 方唯硕

Catalytic Enantioselective Ring Opening of Epoxides

WANG Leia,b ,LI Ye-Zhia,HUANG Hua-Mina,FANG Wei-Shuo*,b   

  1. (a College of Chemistry, Jilin University, Changchun 130023)
    (b Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100050)
  • Received:2005-03-29 Revised:1900-01-01 Published:2006-09-11
  • Contact: FANG Wei-Shuo

手性催化的环氧化物立体选择性开环反应可以用来制备多种具光学活性的化合物, 因而成为有机合成中极为重要的方法之一. 多种亲核试剂都已成功应用于此类反应. 综述了近十年来环氧化物的立体选择性开环反应方面的一些最新研究进展.

关键词: 环氧化物, 立体选择性, 动力学拆分, 开环反应

The enantioselective ring opening of epoxides catalyzed by chiral catalysts has emerged as an important synthetic strategy for the preparation of various optically active compounds. A variety of nucleophiles have been employed successfully in these reactions. This review summarizes the progress in the last ten years.

Key words: enantioselectivity, ring opening, kinetic resolution, epoxide