文献类型：期刊文献

英文题名：Pd-catalyzed cross-coupling reactions of arenediazonium salts with arylsilanes and aryltrifluoroborates in water

作者：Cheng, Kai[1];Zhao, Baoli[1];Hu, Sai[2];Zhang, Xian-Man[1];Qi, Chenze[1]

机构：[1]Shaoxing Univ, Zhejiang Key Lab Alternat Technol Fine Chem Proc, Shaoxing 312000, Peoples R China;[2]Ningbo Univ, Coll Mat Sci & Chem Engn, Ningbo 310014, Zhejiang, Peoples R China

年份：2013

卷号：54

期号：46

起止页码：6211

外文期刊名：TETRAHEDRON LETTERS

收录：SCI-EXPANDED(收录号：WOS:000326009300015)、、Scopus(收录号：2-s2.0-84885481107)、WOS、CCR-EXPANDED(收录号：WOS:000326009300015)

基金：This study was financially supported by the National Science Foundation of China (Grant #21172149), the Science Technology Department of Zhejiang Province (Grant #2012R10014-15) and the Science Technology Project of Shaoxing (Grant.# 2013014017).

语种：英文

外文关键词：Palladium catalyzed cross-coupling; Arenediazonium salts; Environmental-friendly aqueous solution; One-pot domino process

外文摘要：Pd-catalyzed cross-coupling reactions of various arenediazonium salts with ArSi(OR)(3) and KArBF3 have been achieved in good to excellent yields under simple aerobic conditions in water at room temperature. The functional group tolerance makes these transformations as attractive alternatives to the traditional cross-coupling approaches. Furthermore, the sequence can also be performed in a one-pot domino process, omitting the isolation of the intermediate arenediazonium salt. (C) 2013 Elsevier Ltd. All rights reserved.