期刊文献+

Copper(I)-Catalyzed Asymmetric [3+2]-Cycloaddition of α-Substituted Iminoesters with α-Trifluoromethyl α,β-Unsaturated Esters

Copper(I)-Catalyzed Asymmetric [3+2]-Cycloaddition of α-Substituted Iminoesters with α-Trifluoromethyl α,β-Unsaturated Esters
原文传递
导出
摘要 Reported herein is an example of highly regio-, diastereo-and enantioselective Cu(I)-catalyzed intermolecular [3+2] cycloaddition reaction of a-substituted iminoesters with α-trifluoromethyl α,β-unsaturated esters. This novel strategy provided a facile access to pyrrolidines with two skipped (aza)quaternary stereocenters including a CF3 all-carbon quaternary stereocenter. A broad substrate scope was observed and high yields (up to 94%) with excellent diastereoselectivity (up to 〉20 : 1 d.r.) and enantioselectivity (up to 98% ee) were obtained. Reported herein is an example of highly regio-, diastereo-and enantioselective Cu(I)-catalyzed intermolecular [3+2] cycloaddition reaction of a-substituted iminoesters with α-trifluoromethyl α,β-unsaturated esters. This novel strategy provided a facile access to pyrrolidines with two skipped (aza)quaternary stereocenters including a CF3 all-carbon quaternary stereocenter. A broad substrate scope was observed and high yields (up to 94%) with excellent diastereoselectivity (up to 〉20 : 1 d.r.) and enantioselectivity (up to 98% ee) were obtained.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2018年第5期421-429,共9页 中国化学(英文版)
关键词 tminoesters [3+2] cycioaddition (aza)quaternary stereocenters tminoesters [3+2] cycioaddition (aza)quaternary stereocenters
  • 相关文献

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部