首页 | 本学科首页   官方微博 | 高级检索  
     

手性伯胺催化Biginelli反应合成手性嘧啶酮化合物的影响因素研究
引用本文:周伟,赵金刚,林晶,徐燕霞,刘珺,赵淑娟,谢恬. 手性伯胺催化Biginelli反应合成手性嘧啶酮化合物的影响因素研究[J]. 杭州师范大学学报(自然科学版), 2012, 0(4): 352-358
作者姓名:周伟  赵金刚  林晶  徐燕霞  刘珺  赵淑娟  谢恬
作者单位:杭州师范大学生物医药与健康研究中心
基金项目:杭州市重大科技专门项目(20092113A03)
摘    要:手性嘧啶酮类化合物具有重要的药理活性应用.采用手性伯胺与金属盐的复合催化体系催化Bigi-nelli反应,可以得到高立体选择性的手性嘧啶酮化合物.通过对各种反应条件的考察,结果表明,在NbCl5与QN-NH2的协同催化作用下得到较为理想的e.e.值(69%)和产率(74%).

关 键 词:手性嘧啶酮化合物  Biginelli反应  金属  手性伯胺催化剂

The Influencing Factors on the Synthesis of Chiral Pyrimidine Sulfo-Benzophenone Compounds Catalyzed by Chiral Primary Amine-Based Organocatalyst in Biginelli Reaction
ZHOU Wei,ZHAO Jin-gang,LIN Jing,XU Yan-xia,LIU Jun,ZHAO Shu-juan,Xie Tian. The Influencing Factors on the Synthesis of Chiral Pyrimidine Sulfo-Benzophenone Compounds Catalyzed by Chiral Primary Amine-Based Organocatalyst in Biginelli Reaction[J]. , 2012, 0(4): 352-358
Authors:ZHOU Wei  ZHAO Jin-gang  LIN Jing  XU Yan-xia  LIU Jun  ZHAO Shu-juan  Xie Tian
Affiliation:(Center for Biomedicine and Health,Hangzhou Normal University,Hangzhou 311121,China)
Abstract:Chiral pyrimidine ketone compounds have important pharmacological activities and broad applications in many fields.Chiral pyrimidine sulfo-benzophenone compounds with high enantioselectivity were obtained by the Biginelli reaction,which was catalyzed by chiral primary amine and metal salt.The results show that e.e.can be up to 69% and yield can be up to 76% under the influence of synergistic catalysis of NbCl5 and QN-NH2.
Keywords:chiral pyrimidine sulfo-benzophenone compounds  Biginelli reaction  metal  chiral primary amine-based organocatalysts
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