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
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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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