Highly enantioselective synthesis of alpha-fluoro-alpha-nitro esters via organocatalyzed asymmetric Michael addition

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	Highly enantioselective synthesis of alpha-fluoro-alpha-nitro esters via organocatalyzed asymmetric Michael addition
	Cui HF(崔海峰) ; Li P(李鹏) ; Wang XW(王晓伟) ; Chai Z(柴卓) ; Yang YQ(杨映权) ; Cai YP(蔡岳鹏) ; Zhu SZ(朱仕正) ; Zhao G(赵刚)
刊名	Tetrahedron
	2011
卷号	67 期号:2 页码:312-317
ISSN号	0040-4020
其他题名	用有机催化的不对称迈克尔加成反应高对映选择性的合成α-氟-α-硝基酯类化合物
通讯作者	朱仕正 ; 赵刚
英文摘要	Primary amines catalyzed the asymmetric Michael addition of ethyl 2-fluoro-2-nitroacetate to enones to provide chiral alpha-fluoro-alpha-nitro ester ketones with two contiguous stereogenic centers, one of which is a fluorinated quaternary chiral center, with excellent enantioselectivities and in moderate to good yields. Crown Copyright (C) 2010 Published by Elsevier Ltd. All rights reserved.
学科主题	有机氟化学
收录类别	SCI
原文出处	http://dx.doi.org/10.1016/j.tet.2010.11.041
语种	英语
WOS记录号	WOS:000286499000005
公开日期	2013-01-18
内容类型	期刊论文
源URL	[http://202.127.28.38/handle/331003/14512]
专题	上海有机化学研究所_中科院有机氟化学重点实验室
推荐引用方式 GB/T 7714	Cui HF,Li P,Wang XW,et al. Highly enantioselective synthesis of alpha-fluoro-alpha-nitro esters via organocatalyzed asymmetric Michael addition[J]. Tetrahedron,2011,67(2):312-317.
APA	崔海峰.,李鹏.,王晓伟.,柴卓.,杨映权.,...&赵刚.(2011).Highly enantioselective synthesis of alpha-fluoro-alpha-nitro esters via organocatalyzed asymmetric Michael addition.Tetrahedron,67(2),312-317.
MLA	崔海峰,et al."Highly enantioselective synthesis of alpha-fluoro-alpha-nitro esters via organocatalyzed asymmetric Michael addition".Tetrahedron 67.2(2011):312-317.