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叶立德环丙烷化和环氧化反应的立体化学控制(英文)

  • 叶松 ,
  • 唐勇 ,
  • 戴立信
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  • 中国科学院上海有机化学研究所金属有机化学国家重点实验室, 上海 200032
叶松:在博士研究生学习期间,在国际知名刊物(如J.Org.Chem.及J.Am.Chem.Soc.)上发表多篇论文。荣获2002年度中国科学院院长奖学金特别奖。

收稿日期: 2002-12-26

  网络出版日期: 2003-05-10

Stereoselective Ylide Cyclopropanation and Epoxidation

  • YE Song ,
  • TANG Yong ,
  • DAI LiXin
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  • State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, China

Received date: 2002-12-26

  Online published: 2003-05-10

Supported by

supported by the National Natural Sciences Found ation of China(20172066)

摘要

主要研究了硫、碲叶立德环丙烷化和环氧化反应的立体化学控制。通过添加剂、手性辅基、手性试剂等 3种策略,分别控制反应的非对映选择性和对映选择性。对烯丙基硫叶立德的不对称环氧化反应也进行了初步研究

本文引用格式

叶松 , 唐勇 , 戴立信 . 叶立德环丙烷化和环氧化反应的立体化学控制(英文)[J]. 中国科学院大学学报, 2003 , 20(3) : 376 -380 . DOI: 10.7523/j.issn.2095-6134.2003.3.019

Abstract

Focusses on the stereoselective cyclopropanation of sulfonium and telluronium allylide with Michael acceptors.Three strategies (additive, chiral auxiliary or chiral reagent)were developed to improve the diastereoselectivity or enantioselectivity of the ylide cyclopropanation reactions.Some preliminary results of epoxidation reaction of sulfonium allylide were also included.

参考文献

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