Issue 5, 2017, Issue in Progress

Ligand- and copper-free Sonogashira and Heck couplings of (Het)aryl chlorides and bromides catalyzed by palladium nanoparticles supported on in situ generated Al(OH)3

Abstract

The ligand- and copper-free Sonogashira reaction of (Het)aryl halides (Br and Cl) with various terminal alkynes and the Heck coupling of (Het)aryl halides (Br and Cl) with a series of olefins, catalyzed by palladium nanoparticles supported on newly generated Al(OH)3, were developed. The catalyst can be readily recovered and reused 6 times without significant loss of activity and palladium leaching.

Graphical abstract: Ligand- and copper-free Sonogashira and Heck couplings of (Het)aryl chlorides and bromides catalyzed by palladium nanoparticles supported on in situ generated Al(OH)3

Supplementary files

Article information

Article type
Paper
Submitted
18 Oct 2016
Accepted
26 Nov 2016
First published
12 Jan 2017
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2017,7, 2475-2479

Ligand- and copper-free Sonogashira and Heck couplings of (Het)aryl chlorides and bromides catalyzed by palladium nanoparticles supported on in situ generated Al(OH)3

X. Li, X. Gong, Z. Li, H. Chang, W. Gao and W. Wei, RSC Adv., 2017, 7, 2475 DOI: 10.1039/C6RA25416K

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