Highly diastereoselective addition of the lithium enolate of   alpha-diazoacetoacetate to N-sulfinyl imines: Enantioselective synthesis   of 2-oxo and 3-oxo pyrrolidines

doi:10.1021/jo702275a

CORC > 北京大学 > 化学与分子工程学院

	Highly diastereoselective addition of the lithium enolate of alpha-diazoacetoacetate to N-sulfinyl imines: Enantioselective synthesis of 2-oxo and 3-oxo pyrrolidines
	Dong, Changqing ; Mo, Fanyang ; Wang, Jianbo
刊名	journal of organic chemistry
	2008
关键词	C-H INSERTION SUBSTITUTED GAMMA-LACTAMS BETA-AMINO ACIDS STEREOSELECTIVE-SYNTHESIS ASYMMETRIC-SYNTHESIS RING EXPANSION WOLFF REARRANGEMENT CARBONYL-COMPOUNDS CHLOROSULFONYL ISOCYANATE NUCLEOPHILIC-ADDITION
DOI	10.1021/jo702275a
英文摘要	[GRAPHICS] The highly enantioselective synthesis of 2-oxo and 3-oxo pyrrolidines has been achieved by diastereoselective addition of the lithium enolate of alpha-diazoacetoacetate to chiral N-sulfinyl imines, followed by photoinduced Wolff rearrangement or Rh(II)-catalyzed intramolecular N-H insertion.; http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000253595100035&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=8e1609b174ce4e31116a60747a720701 ; Chemistry, Organic; SCI(E); PubMed; 29; ARTICLE; 5; 1971-1974; 73
语种	英语
内容类型	期刊论文
源URL	[http://ir.pku.edu.cn/handle/20.500.11897/199245]
专题	化学与分子工程学院
推荐引用方式 GB/T 7714	Dong, Changqing,Mo, Fanyang,Wang, Jianbo. Highly diastereoselective addition of the lithium enolate of alpha-diazoacetoacetate to N-sulfinyl imines: Enantioselective synthesis of 2-oxo and 3-oxo pyrrolidines[J]. journal of organic chemistry,2008.
APA	Dong, Changqing,Mo, Fanyang,&Wang, Jianbo.(2008).Highly diastereoselective addition of the lithium enolate of alpha-diazoacetoacetate to N-sulfinyl imines: Enantioselective synthesis of 2-oxo and 3-oxo pyrrolidines.journal of organic chemistry.
MLA	Dong, Changqing,et al."Highly diastereoselective addition of the lithium enolate of alpha-diazoacetoacetate to N-sulfinyl imines: Enantioselective synthesis of 2-oxo and 3-oxo pyrrolidines".journal of organic chemistry (2008).