Catalyst-Free Imidation of Allyl Sulfides with Chloramine-T and   Subsequent [2,3]-Sigmatropic Rearrangement

doi:10.1002/cjoc.201200604

CORC > 北京大学 > 化学与分子工程学院

	Catalyst-Free Imidation of Allyl Sulfides with Chloramine-T and Subsequent [2,3]-Sigmatropic Rearrangement
	Jiang Yubo ; Mo Fanyang ; Qiu Di ; Kuang Chunxiang ; Zhang Yan ; Wang Jianbo
刊名	中国化学英文版
	2012
关键词	allyl sulfonamide allyl sulfide transition-metal-free reaction sigmatropic rearrangement nitrene 2,3 SIGMATROPIC REARRANGEMENT SULFUR-COMPOUNDS ENANTIOSELECTIVE SYNTHESIS N-ALLENYLSULFENIMIDES PROPARGYL SULFIDES SULFIMIDATION CARBENOIDS AMINATION OXAZIRIDINE DERIVATIVES
DOI	10.1002/cjoc.201200604
英文摘要	A facile synthesis of various allyl sulfonamides based on imidation of allyl sulfides with chloramine-T and subsequent [2,3]-sigmatropic rearrangement has been achieved without metal catalysts. The reaction completes smoothly within 10 min, providing excellent yields in environment friendly solvent of alcohol. Functional groups such as bromine, hydroxyl, protected amido and aldehyde are tolerant under this condition.; Chemistry, Multidisciplinary; SCI(E); 中国科学引文数据库(CSCD); 0; ARTICLE; 9,SI; 2029-2035; 30
语种	英语
内容类型	期刊论文
源URL	[http://ir.pku.edu.cn/handle/20.500.11897/231473]
专题	化学与分子工程学院
推荐引用方式 GB/T 7714	Jiang Yubo,Mo Fanyang,Qiu Di,et al. Catalyst-Free Imidation of Allyl Sulfides with Chloramine-T and Subsequent [2,3]-Sigmatropic Rearrangement[J]. 中国化学英文版,2012.
APA	Jiang Yubo,Mo Fanyang,Qiu Di,Kuang Chunxiang,Zhang Yan,&Wang Jianbo.(2012).Catalyst-Free Imidation of Allyl Sulfides with Chloramine-T and Subsequent [2,3]-Sigmatropic Rearrangement.中国化学英文版.
MLA	Jiang Yubo,et al."Catalyst-Free Imidation of Allyl Sulfides with Chloramine-T and Subsequent [2,3]-Sigmatropic Rearrangement".中国化学英文版 (2012).