中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Organocatalyzed enantioselective Michael additions of nitroalkanes to enones by using primary-secondary diamine catalysts

文献类型:期刊论文

作者Yang YQ(杨映权) ; Chen XK(陈兴宽) ; Xiao H(肖华) ; Liu W(刘文) ; Zhao G(赵刚)
刊名Chem. Commun.
出版日期2010
卷号46期号:23页码:4130-4132
ISSN号1359-7345
其他题名手性伯-仲二胺催化剂催化的硝基烷烃对烯酮的对映选择性迈克加成反应
通讯作者赵刚
英文摘要Primary-secondary diamines perform as efficient organo-catalysts for the asymmetric addition of nitroalkanes to enones, giving the Michael adducts with excellent yields and enantio-selectivities.
学科主题天然产物有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1039/c002552f
语种英语
WOS记录号WOS:000278364900029
公开日期2013-02-26
源URL[http://202.127.28.38/handle/331003/20793]  
专题上海有机化学研究所_中科院天然产物有机化学重点实验室
推荐引用方式
GB/T 7714
Yang YQ,Chen XK,Xiao H,et al. Organocatalyzed enantioselective Michael additions of nitroalkanes to enones by using primary-secondary diamine catalysts[J]. Chem. Commun.,2010,46(23):4130-4132.
APA 杨映权,陈兴宽,肖华,刘文,&赵刚.(2010).Organocatalyzed enantioselective Michael additions of nitroalkanes to enones by using primary-secondary diamine catalysts.Chem. Commun.,46(23),4130-4132.
MLA 杨映权,et al."Organocatalyzed enantioselective Michael additions of nitroalkanes to enones by using primary-secondary diamine catalysts".Chem. Commun. 46.23(2010):4130-4132.

入库方式: OAI收割

来源:上海有机化学研究所

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