Issue 129, 2015
From the journal:

RSC Advances

Room-temperature palladium-catalysed Suzuki–Miyaura coupling of arylboric acid with aryl chlorides†

Dan Wang,‡a   Hong-Guan Chen,‡a   Xin-Chuan Tian,a   Xiao-Xia Liang,a   Feng-Zhen Chenb  and  Feng Gao*a  

* Corresponding authors

a Department of Chinese Traditional Herbal, Agronomy College, Sichuan Agricultural University, Chengdu 611130, P. R. China
E-mail: gaofeng@sicau.edu.cn

b School of Bioengineering, Chengdu University, Chengdu 610106, P. R.China

Abstract

An efficient room-temperature Pd-catalyzed Suzuki–Miyaura cross-coupling reaction of aryl-boronic acids with aryl chlorides is communicated here. The Pd(OAc)2/NiXantphos catalyst system enables the coupling reaction at room temperature in good to excellent yields (average yield >90%).

Graphical abstract: Room-temperature palladium-catalysed Suzuki–Miyaura coupling of arylboric acid with aryl chlorides

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Article information

DOI
https://doi.org/10.1039/C5RA19790B
Article type
Communication
Submitted
24 Sep 2015
Accepted
07 Dec 2015
First published
09 Dec 2015

RSC Adv., 2015,5, 107119-107122

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Room-temperature palladium-catalysed Suzuki–Miyaura coupling of arylboric acid with aryl chlorides

D. Wang, H. Chen, X. Tian, X. Liang, F. Chen and F. Gao, RSC Adv., 2015, 5, 107119 DOI: 10.1039/C5RA19790B

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