Issue 49, 2014
From the journal:

RSC Advances

Palladium-catalyzed Suzuki cross-couplings of N′-mesyl arylhydrazines via C–N bond cleavage†

He-Ping Zhou,a   Jin-Biao Liu,*ab   Jian-Jun Yuana  and  Yi-Yuan Peng*a  

* Corresponding authors

a Key Laboratory of Green Chemistry, Jiangxi Province and College of Chemistry & Chemical Engineering, Jiangxi Normal University, Nanchang 330022, Jiangxi, PR China
E-mail: liujbgood@hotmail.com, yiyuanpeng@yahoo.com

b School of Metallurgy and Chemical Engineering, Jiangxi University of Science and Technology, 86 Hongqi Road, Ganzhou 341000, Jiangxi, PR China

Abstract

An efficient palladium-catalyzed Suzuki cross-coupling reaction of N′-mesyl arylhydrazine with aryl boronic acid is described, which affords the corresponding biaryl compounds in high yields. This transformation proceeds through C–N bond cleavage under mild conditions.

Graphical abstract: Palladium-catalyzed Suzuki cross-couplings of N′-mesyl arylhydrazines via C–N bond cleavage

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Article information

DOI
https://doi.org/10.1039/C4RA03421J
Article type
Communication
Submitted
15 Apr 2014
Accepted
29 May 2014
First published
29 May 2014

RSC Adv., 2014,4, 25576-25579

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Palladium-catalyzed Suzuki cross-couplings of N′-mesyl arylhydrazines via C–N bond cleavage

H. Zhou, J. Liu, J. Yuan and Y. Peng, RSC Adv., 2014, 4, 25576 DOI: 10.1039/C4RA03421J

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