A practical route for the highly stereoselective synthesis of tetrasubstituted fluoroalkenes

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	A practical route for the highly stereoselective synthesis of tetrasubstituted fluoroalkenes
	Cao CR(曹春如); Ou S(欧松); Jiang M(蒋敏); Liu JT(刘金涛)
刊名	Org. Biomol. Chem.
	2014
卷号	12 期号:3 页码:467-473
其他题名	一种高选择性合成四取代含氟烯烃的实用方法
通讯作者	刘金涛
英文摘要	A series of tetrasubstituted fluoroatkene derivatives were synthesized by the reaction of alpha-fluoro-beta-carbonyl benzothiazol-2-yl sulfones with various nucleophiles in good yields with high stereoselectivities. The predominant cis configuration of fluorine and alkynyl groups was observed. A single isomer was obtained when a ketone, acetate or amide was used as the substrate in the presence of a base.
学科主题	氟化学
收录类别	SCI
原文出处	http://dx.doi.org/10.1039/c3ob42093k
语种	英语
内容类型	期刊论文
源URL	[http://ir.sioc.ac.cn/handle/331003/38832]
专题	上海有机化学研究所_中科院有机氟化学重点实验室
作者单位	中科院上海有机化学研究所
推荐引用方式 GB/T 7714	Cao CR,Ou S,Jiang M,et al. A practical route for the highly stereoselective synthesis of tetrasubstituted fluoroalkenes[J]. Org. Biomol. Chem.,2014,12(3):467-473.
APA	曹春如,欧松,蒋敏,&刘金涛.(2014).A practical route for the highly stereoselective synthesis of tetrasubstituted fluoroalkenes.Org. Biomol. Chem.,12(3),467-473.
MLA	曹春如,et al."A practical route for the highly stereoselective synthesis of tetrasubstituted fluoroalkenes".Org. Biomol. Chem. 12.3(2014):467-473.