Enantioselective synthesis of bicyclo[2.2.2]octane-1-carboxylates under metal free conditions

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	Enantioselective synthesis of bicyclo[2.2.2]octane-1-carboxylates under metal free conditions
	Li YZ(李英姿)1; Wang J(王杰)1; Sun WB(孙网彬)1; Dan YF(单益凡)1; Sun BF(孙炳峰)1; Lin GQ(林国强)1; Zou JP(邹建平)1
刊名	Org. Chem. Front.
	2015
卷号	2 期号:3 页码:274-278
其他题名	无金属催化下的对映选择性合成双环[2.2.2]辛烷-1-羧酸酯
通讯作者	孙炳峰 ; 林国强
英文摘要	A new tandem reaction was realized that permits rapid access to a wide range of bicyclo[2.2.2]octane-1-carboxylates in good to excellent yields with excellent enantioselectivities under metal free, mild, and operationally simple conditions. An open transition state was deemed operative in this highly enantioselective process mediated by an organic base.
学科主题	天然产物有机化学
收录类别	SCI
原文出处	http://dx.doi.org/10.1039/c4qo00311j
语种	英语
WOS记录号	WOS:000364444000014
内容类型	期刊论文
源URL	[http://ir.sioc.ac.cn/handle/331003/39811]
专题	上海有机化学研究所_中科院天然产物有机化学重点实验室
作者单位	1.中科院上海有机化学研究所, 天然产物有机合成化学重点实验室 2.苏州大学
推荐引用方式 GB/T 7714	Li YZ,Wang J,Sun WB,et al. Enantioselective synthesis of bicyclo[2.2.2]octane-1-carboxylates under metal free conditions[J]. Org. Chem. Front.,2015,2(3):274-278.
APA	李英姿.,王杰.,孙网彬.,单益凡.,孙炳峰.,...&邹建平.(2015).Enantioselective synthesis of bicyclo[2.2.2]octane-1-carboxylates under metal free conditions.Org. Chem. Front.,2(3),274-278.
MLA	李英姿,et al."Enantioselective synthesis of bicyclo[2.2.2]octane-1-carboxylates under metal free conditions".Org. Chem. Front. 2.3(2015):274-278.