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Desulfinative palladium-catalyzed cross-coupling of arylsulfonyl hydrazides with aryl bromides under air  ( SCI-EXPANDED收录 EI收录)  

文献类型:期刊文献

英文题名:Desulfinative palladium-catalyzed cross-coupling of arylsulfonyl hydrazides with aryl bromides under air

作者:Liu, Qingling[1];Yang, Bo[1]

第一作者:刘清玲

通讯作者:Liu, QL[1];Yang, B[1]

机构:[1]Xinxiang Univ, Dept Chem & Chem Engn, Xinxiang 453003, Henan, Peoples R China

第一机构:新乡学院化学化工学院

通讯机构:[1]corresponding author), Xinxiang Univ, Dept Chem & Chem Engn, Xinxiang 453003, Henan, Peoples R China.|[110713]新乡学院化学化工学院;[11071]新乡学院;

年份:2019

卷号:33

期号:10

外文期刊名:APPLIED ORGANOMETALLIC CHEMISTRY

收录:;EI(收录号:20193407338444);Scopus(收录号:2-s2.0-85070812029);WOS:【SCI-EXPANDED(收录号:WOS:000482267100001),CCR-EXPANDED(收录号:WOS:000482267100001)】;

基金:This work was supported by 18YCKL028.

语种:英文

外文关键词:aryl bromides; arylsulfonyl hydrazides; biaryls synthesis; Pd-catalyzed cross-coupling

摘要:A highly efficient and mild palladium-catalyzed cross-coupling of arylsulfonyl hydrazides and aryl bromides for the selective synthesis of unsymmetrical biaryls has been developed. This methodology has the advantages of easily accessible starting materials, functional group tolerance and a wide range of substrates, which provide rapid access to biaryls derivatives. In this protocol, abundant and stable aryl bromides serve as the aryl sources by coupling reaction of the aryl group generated from arylsulfonyl hydrazides via in situ release of nitrogen and sulfur dioxide. No external oxidants or acids are needed for this kind of transformation.

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