中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Asymmetric Michael Addition of Trisubstituted Carbanion to Nitroalkenes Catalyzed by Sodium Demethylquinine Salt in Water

文献类型:期刊论文

作者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
出版日期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
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.

入库方式: OAI收割

来源:兰州化学物理研究所

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