Asymmetric 5-endo chloroetherification of homoallylic alcohols toward the synthesis of chiral beta-chlorotetrahydrofurans

doi:10.1039/c2cc38436a

	Asymmetric 5-endo chloroetherification of homoallylic alcohols toward the synthesis of chiral beta-chlorotetrahydrofurans
Department	OSSO国家重点实验室
	Ceng XH(曾祥华)1,2; Miao CX(苗成霞)1 ; Wang SF(王寿峰)1 ; Xia CG(夏春谷)1 ; Sun W(孙伟)1 ; Sun W(孙伟); Xia CG(夏春谷)
	2013
Source Publication	Chemical Communications
ISSN	1359-7345
Volume	49 Issue:24 Pages:2418-2420
Abstract	An asymmetric 5-endo chloroetherification of homoallylic alcohols is successfully developed that employs an easily available quaternary ammonium salt derived from cinchonine as a conventional organocatalyst. This approach provides ready access to β-chlorotetrahydrofurans in high enantioselectivities.
Subject Area	物理化学与绿色催化
DOI	10.1039/c2cc38436a
Funding Organization	the Chinese Academy of Sciences;the National Natural Science Foundation of China (21073210;21133011)
Indexed By	SCI
If	6.718
Language	英语
Funding Project	生物与仿生催化课题组;均相催化课题组
compositor	第一作者单位
Citation statistics	Cited Times:74[WOS] [WOS Record] [Related Records in WOS]
Document Type	期刊论文
Identifier	http://ir.licp.cn/handle/362003/4759
Collection	羰基合成与选择氧化国家重点实验室（OSSO）
Corresponding Author	Sun W(孙伟); Xia CG(夏春谷)
Affiliation	1.Chinese Acad Sci, State Key Lab Oxo Synth & Select Oxidat, Lanzhou Inst Chem Phys, Lanzhou, Peoples R China 2.Chinese Acad Sci, Grad Sch, Beijing, Peoples R China
Recommended Citation GB/T 7714	Ceng XH,Miao CX,Wang SF,et al. Asymmetric 5-endo chloroetherification of homoallylic alcohols toward the synthesis of chiral beta-chlorotetrahydrofurans[J]. Chemical Communications,2013,49(24):2418-2420.
APA	Ceng XH.,Miao CX.,Wang SF.,Xia CG.,Sun W.,...&夏春谷.(2013).Asymmetric 5-endo chloroetherification of homoallylic alcohols toward the synthesis of chiral beta-chlorotetrahydrofurans.Chemical Communications,49(24),2418-2420.
MLA	Ceng XH,et al."Asymmetric 5-endo chloroetherification of homoallylic alcohols toward the synthesis of chiral beta-chlorotetrahydrofurans".Chemical Communications 49.24(2013):2418-2420.

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