Asymmetric Michael Addition of Trisubstituted Carbanion to Nitroalkenes Catalyzed by Sodium Demethylquinine Salt in Water
Chen FX(陈福欣) ; Shao C(邵成) ; Liu Q(刘谦) ; Gong P(龚频) ; Liu CL(刘春良) ; Wang R(王锐)
刊名Chirality
2009
卷号21页码:600-603
关键词organocatalysis nitroalkenes quinine derivate quaternary carbon centers water
ISSN号0899-0042
通讯作者王锐
中文摘要A mild method for the asymmetric synthesis of quaternary and tertiary carbon centers has been developed through Michael addition of trisubstituted carbon nucleophile to nitroalkenes catalyzed by low loading sodium demethylquinine salt in water.
学科主题物理化学
收录类别SCI
资助信息State Key Laboratory of Applied Organic Chemistry and Institute of Biochemistry and Molecular Biology, Lanzhou University, China, Ministry of Education of China;Natural Science Foundation of China (Contract grant numbers: 20525206;20772052;20621091)
语种英语
WOS记录号WOS:000267250300006
公开日期2012-09-21
内容类型期刊论文
源URL[http://210.77.64.217/handle/362003/573]  
专题兰州化学物理研究所_OSSO国家重点实验室
推荐引用方式
GB/T 7714
Chen FX,Shao C,Liu Q,et al. Asymmetric Michael Addition of Trisubstituted Carbanion to Nitroalkenes Catalyzed by Sodium Demethylquinine Salt in Water[J]. Chirality,2009,21:600-603.
APA 陈福欣,邵成,刘谦,龚频,刘春良,&王锐.(2009).Asymmetric Michael Addition of Trisubstituted Carbanion to Nitroalkenes Catalyzed by Sodium Demethylquinine Salt in Water.Chirality,21,600-603.
MLA 陈福欣,et al."Asymmetric Michael Addition of Trisubstituted Carbanion to Nitroalkenes Catalyzed by Sodium Demethylquinine Salt in Water".Chirality 21(2009):600-603.
个性服务
查看访问统计
相关权益政策
暂无数据
收藏/分享
所有评论 (0)
暂无评论
 

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。


©版权所有 ©2017 CSpace - Powered by CSpace