Highly stereoselective [2,3]-sigmatropic rearrangement of sulfur ylide   generated through Cu(I) carbene and sulfides

doi:10.1021/ja055021d

CORC > 北京大学 > 化学与分子工程学院

	Highly stereoselective [2,3]-sigmatropic rearrangement of sulfur ylide generated through Cu(I) carbene and sulfides
	Ma, M ; Peng, LL ; Li, CK ; Zhang, X ; Wang, JB
刊名	journal of the american chemical society
	2005
关键词	2,3 SIGMATROPIC REARRANGEMENT < ASYMMETRIC-SYNTHESIS CATALYTIC METHODS DIAZO-COMPOUNDS ALLYL SULFIDES CYCLOPROPANATION AZIRIDINATION COMPLEXES LIGANDS 2,3> -SIGMATROPIC REARRANGEMENT
DOI	10.1021/ja055021d
英文摘要	A highly stereoselective [2,3]-sigmatropic rearrangement of sulfur ylide generated through Cu(I) carbene and allyl and propargyl sulfides by a double asymmetric induction approach that combines a chiral camphor sultam auxiliary and Cu(I) catalyst with chiral or achiral diimine ligands has been developed.; Chemistry, Multidisciplinary; SCI(E); EI; PubMed; 56; ARTICLE; 43; 15016-15017; 127
语种	英语
内容类型	期刊论文
源URL	[http://ir.pku.edu.cn/handle/20.500.11897/345927]
专题	化学与分子工程学院
推荐引用方式 GB/T 7714	Ma, M,Peng, LL,Li, CK,et al. Highly stereoselective [2,3]-sigmatropic rearrangement of sulfur ylide generated through Cu(I) carbene and sulfides[J]. journal of the american chemical society,2005.
APA	Ma, M,Peng, LL,Li, CK,Zhang, X,&Wang, JB.(2005).Highly stereoselective [2,3]-sigmatropic rearrangement of sulfur ylide generated through Cu(I) carbene and sulfides.journal of the american chemical society.
MLA	Ma, M,et al."Highly stereoselective [2,3]-sigmatropic rearrangement of sulfur ylide generated through Cu(I) carbene and sulfides".journal of the american chemical society (2005).