Synthesis of chiral gamma-sultams through intramolecular reductive amination with sulfonylcarbamate as N-source

doi:10.1016/j.tetlet.2017.03.012

	Synthesis of chiral gamma-sultams through intramolecular reductive amination with sulfonylcarbamate as N-source
	Song, Bo 1,2; Ji, Yue 2; Hu, Shu-Bo 2; Yu, Chang-Bin 2; Zhou, Yong-Gui 2
刊名	TETRAHEDRON LETTERS
	2017-04-12
卷号	58 页码:1528-1530
关键词	Palladium Reductive Amination Sulfonylcarbamate Chiral Gamma-sultams
DOI	10.1016/j.tetlet.2017.03.012
英文摘要	An efficient and enantioselective palladium-catalyzed intramolecular asymmetric reductive amination with sulfonylcarbamates as N-sources was reported, providing a facile and general access to the chiral gamma-sultam derivatives with up to 97% of enantioselectivity. This tandem process avoids additional deprotection manipulation and arduous isolation of the N-sulfonyl-imine intermediates. (C) 2017 Elsevier Ltd. All rights reserved.
语种	英语
WOS记录号	WOS:000399517600026
内容类型	期刊论文
源URL	[http://cas-ir.dicp.ac.cn/handle/321008/152320]
专题	大连化学物理研究所_中国科学院大连化学物理研究所
作者单位	1.Univ Chinese Acad Sci, Beijing 100049, Peoples R China 2.Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, 457 Zhongshan Rd, Dalian 116023, Peoples R China
推荐引用方式 GB/T 7714	Song, Bo,Ji, Yue,Hu, Shu-Bo,et al. Synthesis of chiral gamma-sultams through intramolecular reductive amination with sulfonylcarbamate as N-source[J]. TETRAHEDRON LETTERS,2017,58:1528-1530.
APA	Song, Bo,Ji, Yue,Hu, Shu-Bo,Yu, Chang-Bin,&Zhou, Yong-Gui.(2017).Synthesis of chiral gamma-sultams through intramolecular reductive amination with sulfonylcarbamate as N-source.TETRAHEDRON LETTERS,58,1528-1530.
MLA	Song, Bo,et al."Synthesis of chiral gamma-sultams through intramolecular reductive amination with sulfonylcarbamate as N-source".TETRAHEDRON LETTERS 58(2017):1528-1530.