期刊文献+

Enantioselective Conjugate Addition of Diethylzinc to Chalcone Catalyzed by Ni(acac)_2 and Chiral β-Amino Alcohols

Enantioselective Conjugate Addition of Diethylzinc to Chalcone Catalyzed by Ni(acac)_2 and Chiral β-Amino Alcohols
原文传递
导出
摘要 Enantioselective conjugate addition of diethylzinc to chalcone was carried out in the presence of Ni(acac) 2 complexed with five pyrrolidinylmethanols derived from L proline. ( S ) N Benzyl 2 (1 hydroxy 1 methylethyl) pyrrolidine was found to be the best ligand in asymmetric conjugate addition among the five ligands. The products were obtained with up to 70% ee . The configuration of the product was determined jointly by the substituents on the carbon of the hydroxy group and the nitrogen atom. Enantioselective conjugate addition of diethylzinc to chalcone was carried out in the presence of Ni(acac) 2 complexed with five pyrrolidinylmethanols derived from L proline. ( S ) N Benzyl 2 (1 hydroxy 1 methylethyl) pyrrolidine was found to be the best ligand in asymmetric conjugate addition among the five ligands. The products were obtained with up to 70% ee . The configuration of the product was determined jointly by the substituents on the carbon of the hydroxy group and the nitrogen atom.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2003年第8期1105-1107,共3页 中国化学(英文版)
基金 theNationalNaturalScienceFoundationofChina (No .2 9972 0 16andQTProgram ) theTeachingandResearchAwardProgramforOutstandingYoungTeachersinHigherEducationInstitutionsoftheMinistryofEducationofChina
关键词 asymmetric conjugation addition Ni(acac) 2 pyrrolidinylmethanols asymmetric conjugation addition, Ni(acac) 2, pyrrolidinylmethanols
  • 相关文献

参考文献1

共引文献1

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