Synthesis of Aryl Trimethylstannanes from Aryl Amines: A Sandmeyer-Type   Stannylation Reaction

doi:10.1002/anie.201304579

CORC > 北京大学 > 化学与分子工程学院

	Synthesis of Aryl Trimethylstannanes from Aryl Amines: A Sandmeyer-Type Stannylation Reaction
	Qiu, Di ; Meng, He ; Jin, Liang ; Wang, Shuai ; Tang, Shengbo ; Wang, Xi ; Mo, Fanyang ; Zhang, Yan ; Wang, Jianbo
刊名	angewandte chemie international edition
	2013
关键词	aryl stannanes cross-coupling diazonium salts Sandmeyer reaction Stille coupling reaction CROSS-COUPLING REACTIONS METAL-FREE BORYLATION ORGANIC HALIDES ORGANOTIN COMPOUNDS DIRECT CONVERSION RADICAL-ADDITION DIAZONIUM SALTS ALKYL NITRITES PALLADIUM ARYLAMINES
DOI	10.1002/anie.201304579
英文摘要	Sandmeyer-type stannylation: Stille coupling is one of the most powerful coupling reactions for C?C bond formation, whereas there are only limited methods to access aryl stannane compounds. A mild stannylation process based on a Sandmeyer-type transformation using aromatic amines as the starting materials is described. DCE: 1,2-dichloroethane.Copyright ? 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.; http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000330732700022&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=8e1609b174ce4e31116a60747a720701 ; Chemistry, Multidisciplinary; SCI(E); PubMed; 36; ARTICLE; 44; 11581-11584; 52
语种	英语
内容类型	期刊论文
源URL	[http://ir.pku.edu.cn/handle/20.500.11897/189979]
专题	化学与分子工程学院
推荐引用方式 GB/T 7714	Qiu, Di,Meng, He,Jin, Liang,et al. Synthesis of Aryl Trimethylstannanes from Aryl Amines: A Sandmeyer-Type Stannylation Reaction[J]. angewandte chemie international edition,2013.
APA	Qiu, Di.,Meng, He.,Jin, Liang.,Wang, Shuai.,Tang, Shengbo.,...&Wang, Jianbo.(2013).Synthesis of Aryl Trimethylstannanes from Aryl Amines: A Sandmeyer-Type Stannylation Reaction.angewandte chemie international edition.
MLA	Qiu, Di,et al."Synthesis of Aryl Trimethylstannanes from Aryl Amines: A Sandmeyer-Type Stannylation Reaction".angewandte chemie international edition (2013).