中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Asymmetric Addition of Terminal Alkynes to N-(Diphenylphosphinoyl)imines Promoted by Stoichiometric Amounts of a Proline-Derived beta-Amino Alcohol

文献类型:期刊论文

作者Yan WJ(阎文锦) ; Mao B(毛斌) ; Zhu SQ(朱绍群) ; Jiang XX(蒋先兴) ; Liu ZL(刘中立) ; Wang R(王锐)
刊名European Journal of Organic Chemistry
出版日期2009
页码3790-3794
关键词Enantioslectivity Asymmetric synthesis Alkynylation β-Amino alcohol Propargylamines
ISSN号1466-8033
通讯作者王锐
中文摘要A new synthetic methodology for the preparation of optically active propargylamines is described. The alkynylation of aromatic, heteroaromatic, aliphatic and α,β-unsaturated N-(diphenylphosphinoyl) imines was investigated by using diethylzinc and a proline-derived β-amino alcohol. N-(Diphenyl-phosphinoyl)-protected propargylic amines can be synthesized in high yields and with good to excellent enantioselectivities.
学科主题物理化学
收录类别SCI
资助信息the National Natural Science Foundation of China (20525206;20772052;90813012;20621091);the Chang Jiang Program of the Ministry of Education of China
语种英语
WOS记录号WOS:000268659900016
公开日期2012-09-21
源URL[http://210.77.64.217/handle/362003/556]  
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
Yan WJ,Mao B,Zhu SQ,et al. Asymmetric Addition of Terminal Alkynes to N-(Diphenylphosphinoyl)imines Promoted by Stoichiometric Amounts of a Proline-Derived beta-Amino Alcohol[J]. European Journal of Organic Chemistry,2009:3790-3794.
APA 阎文锦,毛斌,朱绍群,蒋先兴,刘中立,&王锐.(2009).Asymmetric Addition of Terminal Alkynes to N-(Diphenylphosphinoyl)imines Promoted by Stoichiometric Amounts of a Proline-Derived beta-Amino Alcohol.European Journal of Organic Chemistry,3790-3794.
MLA 阎文锦,et al."Asymmetric Addition of Terminal Alkynes to N-(Diphenylphosphinoyl)imines Promoted by Stoichiometric Amounts of a Proline-Derived beta-Amino Alcohol".European Journal of Organic Chemistry (2009):3790-3794.

入库方式: OAI收割

来源:兰州化学物理研究所

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