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一种新型手性席夫碱的合成及其在不对称环丙烷化反应中的催化性能
引用本文:李琛,张维萍,姚小泉,刘秀梅,陆世维,韩秀文,包信和.一种新型手性席夫碱的合成及其在不对称环丙烷化反应中的催化性能[J].催化学报,2000,21(3):289-292.
作者姓名:李琛  张维萍  姚小泉  刘秀梅  陆世维  韩秀文  包信和
作者单位:中国科学院大连化学物理研究所催化基础国家重点实验室,大连,116023
摘    要:在不对称催化的发展过程中,设计与合成新的手性配体一直是人们所关注的热点,并已取得很大的进展1].

关 键 词:不对称环丙烷化  手性席夫碱  手性配体  均相
收稿时间:2000-06-25

Synthesis of a New C2-Symmetric Chiral Schiff Base and Its Catalytic Performance in Asymmetric Cyclopropanation
LI Chen,ZHANG Weiping,YAO Xiaoquan,LIU Xiumei,LU Shiwei,HAN Xiuwen,BAO Xinhe.Synthesis of a New C2-Symmetric Chiral Schiff Base and Its Catalytic Performance in Asymmetric Cyclopropanation[J].Chinese Journal of Catalysis,2000,21(3):289-292.
Authors:LI Chen  ZHANG Weiping  YAO Xiaoquan  LIU Xiumei  LU Shiwei  HAN Xiuwen  BAO Xinhe
Abstract:A new C 2 symmetric chiral Schiff base compound A with relatively flexible chiral environment was synthesized from L (+) tartaric acid. Its structure was determined by NMR, IR, MS etc, and its preponderant conformation was modeled by CS Chem 3D Program. The results showed that its structure is not in a plane and has a big chiral cavity. It was showed that the complex B has different catalytic performance in asymmetric cyclopropanation of styrene and DMHD (2,5 dimethyl 2,4 hexadiene) with diazoacetate. The catalytic mechanism was also discussed.
Keywords:olefin  asymmetric cyclopropanation  chiral Schiff base  tartaric acid  nuclear magnetic resonance  
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