Issue 20, 2013

An improved iron-mediated synthesis of N-2-aryl substituted 1,2,3-triazoles

Abstract

Treatment of various chalcones and sodium azide in the presence of catalytic amounts of commercially available iron oxide nanoparticles, followed by the addition of aryl halides afforded N-2-arylated 1,2,3-triazoles in very good yields. This tandem three-component reaction involves an oxidative 1,3-dipolar cycloaddition of the chalcone and azide and subsequent regioselective N-2-arylation. The nano-catalyst is easily recoverable and can be reused without any significant loss in catalytic activity.

Graphical abstract: An improved iron-mediated synthesis of N-2-aryl substituted 1,2,3-triazoles

Supplementary files

Article information

Article type
Paper
Submitted
11 Oct 2012
Accepted
28 Feb 2013
First published
28 Feb 2013

RSC Adv., 2013,3, 7419-7426

An improved iron-mediated synthesis of N-2-aryl substituted 1,2,3-triazoles

A. Kamal and P. Swapna, RSC Adv., 2013, 3, 7419 DOI: 10.1039/C3RA22485F

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