Issue 78, 2014

Nanoparticle mediated organic synthesis (NAMO-synthesis): CuI-NP catalyzed ligand free amidation of aryl halides

Abstract

The first CuI-nanoparticle catalyzed ligand free synthesis of N-aryl amides from aryl halides and arylamides/cyclic amides has been developed. This methodology is further extended for the synthesis of nitrogen heterocycles such as benzimidazole, and quinazolinone via intermolecular amidation reaction followed by cyclization. TEM images of the CuI-NP catalyst showed spherical, well-dispersed particles which provide large surface area for reactivity and have good recyclability.

Graphical abstract: Nanoparticle mediated organic synthesis (NAMO-synthesis): CuI-NP catalyzed ligand free amidation of aryl halides

Supplementary files

Article information

Article type
Communication
Submitted
08 Jul 2014
Accepted
26 Aug 2014
First published
26 Aug 2014

RSC Adv., 2014,4, 41631-41635

Author version available

Nanoparticle mediated organic synthesis (NAMO-synthesis): CuI-NP catalyzed ligand free amidation of aryl halides

A. Kumar and A. K. Bishnoi, RSC Adv., 2014, 4, 41631 DOI: 10.1039/C4RA06804A

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