首页 | 本学科首页   官方微博 | 高级检索  
     检索      

Study on the stannous halides promoted addition of 1,1,1-trichloro-2,2,2-trifluoroethane to aldehydes and the chemical transformation thereof
作者姓名:HU  Chang-Ming CHEN  JianShanghai Institute of Organic Chemistry  Chinese Academy of Sciences  Shanghai  China
作者单位:HU,Chang-Ming CHEN,JianShanghai Institute of Organic Chemistry,Chinese Academy of Sciences,Shanghai 200032,China
基金项目:Project supported by the National Natural Science Foundation of China.
摘    要:Promoted by stannous salts, 1,1,1-trichloro-2,2,2-trifluoroethane reacts readily with aliphatic, aromatic, and α, β-unsaturated aldehydes giving the corresponding alcohols bearing a CF3CCl2-moiety in good to excellent yields. These alcohols are farther oxidized by Jones reagent giving the corresponding ketones in high yields.


Study on the stannous halides promoted addition of 1,1,1-trichloro-2,2,2-trifluoroethane to aldehydes and the chemical transformation thereof
HU,Chang-Ming CHEN,JianShanghai Institute of Organic Chemistry,Chinese Academy of Sciences,Shanghai ,China.Study on the stannous halides promoted addition of 1,1,1-trichloro-2,2,2-trifluoroethane to aldehydes and the chemical transformation thereof[J].Chinese Journal of Chemistry,1994,12(2):183-189.
Authors:HU  Chang-Ming CHEN  Jian
Institution:HU,Chang-Ming CHEN,JianShanghai Institute of Organic Chemistry,Chinese Academy of Sciences,Shanghai 200032,China
Abstract:Promoted by stannous salts, 1,1,1-trichloro-2,2,2-trifluoroethane reacts readily with aliphatic, aromatic, and α,β-unsaturated aldehydes giving the corresponding alcohols bearing a CF3CCl2-moiety in good to excellent yields. These alcohols are further oxidized by Jones reagent giving the corresponding ketones in high yields.
Keywords:1  1  1-Trichloro-2  2  2-trifluoroethane  aldehydes  stannous halides  addition  Jones oxidation  ketones  
本文献已被 CNKI 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号