中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Asymmetric synthesis of trifluoromethylated propargylamines via 1,2-additions of trifluoromethylacetylide to N-tert-butanesulfinyl imines

文献类型:期刊论文

作者Chen XY(陈先印) ; Qiu XL(邱小龙) ; Qing FL(卿凤翎)
刊名Tetrahedron
出版日期2008
卷号64期号:10页码:2301-2306
ISSN号0040-4020
其他题名Asymmetric synthesis of trifluoromethylated propargylamines via 1,2-additions of trifluoromethylacetylide to N-tert-butanesulfinyl imines
通讯作者卿凤翎
英文摘要An efficient method for the asymmetric synthesis of the trifluoromethylated propargylamines was described. Addition of lithium trifluoromethylacetylide, in situ prepared from lithium diisopropylamide and the 2-bromo-3,3,3-trifluoropropene, to various N-tert-butanesulfinyl imines provided a range of trifluoromethylated propargyl sulfinamides. Besides high yields and excellent diastereoselectivities, the additions featured that the diastereoselectivities could be reversed when polar or nonpolar solvent was used. Acidic cleavage of the tert-butanesulfinyl groups delivered highly optically pure trifluoromethylated propargylamines. (C) 2008 Elsevier Ltd. All rights reserved.
学科主题氟化学
收录类别SCI
原文出处http://dx.doi.org/10.1016/j.tet.2008.01.021
语种英语
WOS记录号WOS:000253432600002
公开日期2013-02-22
源URL[http://202.127.28.38/handle/331003/17645]  
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
Chen XY,Qiu XL,Qing FL. Asymmetric synthesis of trifluoromethylated propargylamines via 1,2-additions of trifluoromethylacetylide to N-tert-butanesulfinyl imines[J]. Tetrahedron,2008,64(10):2301-2306.
APA 陈先印,邱小龙,&卿凤翎.(2008).Asymmetric synthesis of trifluoromethylated propargylamines via 1,2-additions of trifluoromethylacetylide to N-tert-butanesulfinyl imines.Tetrahedron,64(10),2301-2306.
MLA 陈先印,et al."Asymmetric synthesis of trifluoromethylated propargylamines via 1,2-additions of trifluoromethylacetylide to N-tert-butanesulfinyl imines".Tetrahedron 64.10(2008):2301-2306.

入库方式: OAI收割

来源:上海有机化学研究所

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