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

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	Asymmetric 5-endo chloroetherification of homoallylic alcohols toward the synthesis of chiral beta-chlorotetrahydrofurans
	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
刊名	Chemical Communications
	2013
卷号	49 期号:24 页码:2418-2420
ISSN号	1359-7345
通讯作者	孙伟 ; 夏春谷
英文摘要	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.
学科主题	物理化学与绿色催化
收录类别	SCI
资助信息	the Chinese Academy of Sciences;the National Natural Science Foundation of China (21073210;21133011)
语种	英语
WOS记录号	WOS:000315355900010
公开日期	2013-12-18
内容类型	期刊论文
源URL	[http://210.77.64.217/handle/362003/4759]
专题	兰州化学物理研究所_OSSO国家重点实验室
作者单位	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
推荐引用方式 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.(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.