中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Design and synthesis of a tridentate ligand inspired by the phenomenon of self-assembly catalysis and its application in the asymmetric alkynylation of N-(diphenylphosphinoyl) imines

文献类型:期刊论文

作者Yan WJ(阎文锦) ; Li P(李鹏) ; Feng JC(冯静超) ; Wang D(王东) ; Zhu SQ(朱绍群) ; Jiang XX(蒋先兴) ; Wang R(王锐)
刊名Tetrahedron: Asymmetry
出版日期2010
卷号21页码:2037-2042
ISSN号0957-4166
通讯作者王锐
中文摘要On the basis of the phenomenon of self-assembly catalysis, a tridentate ligand was designed and synthesized in two steps. The application in alkynylation of N-(diphenylphosphinoyl) imines gave the expected products. Aromatic, heteroaromatic N-(diphenylphosphinoyl) imines were employed and gave optically active propargylic amines in good yields (up to 89%) and excellent enantioselectivities (up to 96%) by a simple experimental procedure. The direct use of sulfone amides in the alkynylation of N-(diphenylphosphinoyl) aliphatic imines made this method very attractive.
学科主题物理化学
收录类别SCI
资助信息the National Natural Science Foundation of China (Nos. 20932003 ;90813012);the National S & T Major Project of China (2009ZX09503-017)
语种英语
WOS记录号WOS:000281977500015
公开日期2012-09-21
源URL[http://210.77.64.217/handle/362003/515]  
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,Li P,Feng JC,et al. Design and synthesis of a tridentate ligand inspired by the phenomenon of self-assembly catalysis and its application in the asymmetric alkynylation of N-(diphenylphosphinoyl) imines[J]. Tetrahedron: Asymmetry,2010,21:2037-2042.
APA 阎文锦.,李鹏.,冯静超.,王东.,朱绍群.,...&王锐.(2010).Design and synthesis of a tridentate ligand inspired by the phenomenon of self-assembly catalysis and its application in the asymmetric alkynylation of N-(diphenylphosphinoyl) imines.Tetrahedron: Asymmetry,21,2037-2042.
MLA 阎文锦,et al."Design and synthesis of a tridentate ligand inspired by the phenomenon of self-assembly catalysis and its application in the asymmetric alkynylation of N-(diphenylphosphinoyl) imines".Tetrahedron: Asymmetry 21(2010):2037-2042.

入库方式: OAI收割

来源:兰州化学物理研究所

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