Issue 3, 2012
From the journal:

Organic & Biomolecular Chemistry

Suzuki–Miyaura cross-couplings of arenediazonium tetrafluoroborate salts with arylboronic acids catalyzed by aluminium hydroxide-supported palladium nanoparticles†

Xing Li,*a   Xu-Ying Yan,a   Hong-Hong Chang,*a   Li-Chao Wang,a   Yan Zhang,a   Wen-Wen Chen,a   Yan-Wei Lia  and  Wen-Long Weia  

* Corresponding authors

a Department of Chemistry and Chemical Engineering, Taiyuan University of Technology, 79 West Yingze Street, Taiyuan, People's Republic of China
E-mail: lixing@tyut.edu.cn
Fax: +86-351-6111165
Tel: +86-351-6111165

Abstract

Suzuki–Miyaura cross-couplings of arenediazonium salts with arylboronic acids catalyzed by highly active aluminium hydroxide-supported palladium nanoparticles catalyst have been investigated for the first time. The reactions are performed at 25 °C in MeOH without any base and ligand to afford biaryls in good to excellent yields under non-anhydrous and non-degassed conditions.

Graphical abstract: Suzuki–Miyaura cross-couplings of arenediazonium tetrafluoroborate salts with arylboronic acids catalyzed by aluminium hydroxide-supported palladium nanoparticles

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Article information

DOI
https://doi.org/10.1039/C1OB06752D
Article type
Communication
Submitted
19 Oct 2011
Accepted
27 Oct 2011
First published
18 Nov 2011

Org. Biomol. Chem., 2012,10, 495-497

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Suzuki–Miyaura cross-couplings of arenediazonium tetrafluoroborate salts with arylboronic acids catalyzed by aluminium hydroxide-supported palladium nanoparticles

X. Li, X. Yan, H. Chang, L. Wang, Y. Zhang, W. Chen, Y. Li and W. Wei, Org. Biomol. Chem., 2012, 10, 495 DOI: 10.1039/C1OB06752D

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