Chiral phosphine-catalyzed regio- and enantioselective allylic amination of Morita-Baylis-Hillman acetates

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	Chiral phosphine-catalyzed regio- and enantioselective allylic amination of Morita-Baylis-Hillman acetates
	Ma GN(马光宁) ; Cao SH(曹书华) ; Shi M(施敏)
刊名	Tetrahedron-Asymmetry
	2009
卷号	20 期号:9 页码:1086-1092
其他题名	手性膦催化的MBH加成产物的区域和不对称烯丙基胺化反应
通讯作者	施敏
英文摘要	Enantioselective allylic substitution of Morita-Baylis-Hillman (MBH) acetates with phthalimide was realized in the presence of a novel L-proline-derived chiral trifunctional phosphine amide ligand to give the corresponding allylic amination adducts in good yields (70-95%) and in modest to good enantioselectivities (34-78% ee's). (c) 2009 Elsevier Ltd. All rights reserved.
学科主题	金属有机化学
收录类别	SCI
原文出处	http://dx.doi.org/10.1016/j.tetasy.2009.03.040
语种	英语
WOS记录号	WOS:000266735800017
公开日期	2013-01-09
内容类型	期刊论文
源URL	[http://202.127.28.38/handle/331003/10280]
专题	上海有机化学研究所_金属有机化学国家重点实验室
推荐引用方式 GB/T 7714	Ma GN,Cao SH,Shi M. Chiral phosphine-catalyzed regio- and enantioselective allylic amination of Morita-Baylis-Hillman acetates[J]. Tetrahedron-Asymmetry,2009,20(9):1086-1092.
APA	Ma GN,Cao SH,&Shi M.(2009).Chiral phosphine-catalyzed regio- and enantioselective allylic amination of Morita-Baylis-Hillman acetates.Tetrahedron-Asymmetry,20(9),1086-1092.
MLA	Ma GN,et al."Chiral phosphine-catalyzed regio- and enantioselective allylic amination of Morita-Baylis-Hillman acetates".Tetrahedron-Asymmetry 20.9(2009):1086-1092.