Highly Enantioselective [3+2]-Annulation of Isatin-Derived Morita-Baylis-Hillman Adducts with Cyclic Sulfonimines

	Highly Enantioselective [3+2]-Annulation of Isatin-Derived Morita-Baylis-Hillman Adducts with Cyclic Sulfonimines
	Wei, Feng ; Huang, Hong-Yon ; Zhong, Neng-Jun ; Gu, Chun-Ling ; Wang, Dong ; Liu, Li 1
刊名	ORGANIC LETTERS
	2015-04-03
卷号	17 期号:7 页码:1688-1691
英文摘要	An organocatalytic [3 + 2]-annulation between isatin-derived Morita-Baylis-Hillman adducts and cyclic sulfonimines has been developed in high yields with excellent enantio- and diastereoselectivities via an allylic nitrogen-ylide intermediate. The reaction provides access to heavily substituted aza-spirooxindole derivatives, which also contain ring fused cyclic sultams.
收录类别	SCI
语种	英语
公开日期	2015-11-03
内容类型	期刊论文
源URL	[http://ir.iccas.ac.cn/handle/121111/28557]
专题	化学研究所_分子识别与功能实验室
作者单位	1.Chinese Acad Sci, BNLMS, CAS Key Lab Mol Recognit & Funct, Inst Chem, Beijing 100190, Peoples R China 2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
推荐引用方式 GB/T 7714	Wei, Feng,Huang, Hong-Yon,Zhong, Neng-Jun,et al. Highly Enantioselective [3+2]-Annulation of Isatin-Derived Morita-Baylis-Hillman Adducts with Cyclic Sulfonimines[J]. ORGANIC LETTERS,2015,17(7):1688-1691.
APA	Wei, Feng,Huang, Hong-Yon,Zhong, Neng-Jun,Gu, Chun-Ling,Wang, Dong,&Liu, Li.(2015).Highly Enantioselective [3+2]-Annulation of Isatin-Derived Morita-Baylis-Hillman Adducts with Cyclic Sulfonimines.ORGANIC LETTERS,17(7),1688-1691.
MLA	Wei, Feng,et al."Highly Enantioselective [3+2]-Annulation of Isatin-Derived Morita-Baylis-Hillman Adducts with Cyclic Sulfonimines".ORGANIC LETTERS 17.7(2015):1688-1691.