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手性双季铵盐诱导下的硝基甲烷与查尔酮的Michael反应
引用本文:陈继俊,杜争鸣,施耀曾,朱文胜,胡宏纹.手性双季铵盐诱导下的硝基甲烷与查尔酮的Michael反应[J].有机化学,1992(6).
作者姓名:陈继俊  杜争鸣  施耀曾  朱文胜  胡宏纹
作者单位:南京大学化学系,南京大学化学系,南京大学化学系,南京大学化学系,南京大学化学系 南京,210008,南京,210008,南京,210008,南京,210008,南京,210008
摘    要:双季铵盐相转移催化剂具有用量少、催化活性高的特点,比单官能团相转移催化剂的催化性能更为显著。手性季铵盐是进行不对称

关 键 词:不对称诱导  双季铵盐  Michael加成

Chiral Bis-quaternary Ammonium Salts Induction Michael Addition of Nitromethane and Chalcone
CHEN Ji-Jun,DU Zhen-Ming,SHI Yao-Zeng,ZHU Wen-Sheng,HU Hong-Wen.Chiral Bis-quaternary Ammonium Salts Induction Michael Addition of Nitromethane and Chalcone[J].Chinese Journal of Organic Chemistry,1992(6).
Authors:CHEN Ji-Jun  DU Zhen-Ming  SHI Yao-Zeng  ZHU Wen-Sheng  HU Hong-Wen
Institution:CHEN Ji-Jun,DU Zhen-Ming,SHI Yao-Zeng,ZHU Wen-Sheng,HU Hong-Wen Department of Chemistry,Nanjing University,210008 Nanjing
Abstract:The chiral bis-quaternary ammonium salts, 1,8-bis (1S,2R)-N-(2-hydroxy-1- methyl-2-phenyl) et y1-N, N-dimethylammonium]-3, 6-dioxaoctane diiodide (BDMEO I) and 1,11-bis (1S,2R)-N-(2-hydroxy-1-methyl-2-phenyl) ethyl-N, N-dimethylammonium]-3, 6,9-trioxaundecane diiodide (BDMEU I), were synthesized and their selectivity was stu- died in Michael addition of nitromethane and chalcone. The enantiomeric excess was 27.0% The effect of solvents on the stereoselectivity was also discussed.
Keywords:asymmetric induction  bis-quaternary ammonium salt  Michael addition  
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