首页 | 本学科首页   官方微博 | 高级检索  
     

联二萘酚衍生的手性二胺催化剂催化的丙酮与α酮酸酯不对称Aldol反应及机理研究
引用本文:夏友付,刘全忠,邵周恒,赵晶. 联二萘酚衍生的手性二胺催化剂催化的丙酮与α酮酸酯不对称Aldol反应及机理研究[J]. 西华师范大学学报(哲学社会科学版), 2009, 30(2): 216-219
作者姓名:夏友付  刘全忠  邵周恒  赵晶
作者单位:西华师范大学化学化工学院,四川南充637002
摘    要:报道了一种新型的手性二胺化合物,催化丙酮与α酮酸酯的不对称直接Aldol反应,以高达99%的产率和96%的对映选择性得到手性三级醇化合物.通过密度泛涵方法计算得到了四个立体异构过渡态的优化构型及其相对能量,推测了该不对称反应的立体选择性.

关 键 词:手性二胺  aldol反应  密度泛涵方法  机理

The Mechanistic Study in the Asymmetric Direct Aldol Reaction between α-Keto Esters and Acetone
XIA You-fu,LIU Quan-zhong,SHAO Zhou-heng,ZHAO Jing. The Mechanistic Study in the Asymmetric Direct Aldol Reaction between α-Keto Esters and Acetone[J]. Journal of China West Normal University:Natural Science Edition, 2009, 30(2): 216-219
Authors:XIA You-fu  LIU Quan-zhong  SHAO Zhou-heng  ZHAO Jing
Affiliation:College of Chemistry and Chemical Eengineering;China West Normal University;Nanchong 637002;China
Abstract:A novel type of chiral diamines compound has been reported for the asymmetric aldol reaction between acetone and α- keto ester, which furnishes the chiral teriary alcohols up to 99% yield and up to 96% ee. DFT calculations were applied to simulate the possible transition states, and the relative energies for each transition state were obtained. The calculation results revealed the origin of enantionselectivity of the reaction.
Keywords:chiral diamines  aldol reaction  DFT  mechanism  
本文献已被 CNKI 维普 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