Issue 13, 2015
From the journal:

RSC Advances

Copper catalysed C–N bond formation via a sequential acylation and deacylation process: a novel strategy for the synthesis of benzanilides†

Saurabh Kumar,a   Rajeshwer Vanjari,a   Tirumaleswararao Guntreddia  and  Krishna Nand Singh*a  

* Corresponding authors

a Department of Chemistry (Centre of Advanced Study), Faculty of Science, Banaras Hindu University, Varanasi-221005, India
E-mail: knsingh@bhu.ac.in, knsinghbhu@yahoo.co.in

Abstract

An efficient and mild oxidative amidation of aldehydes by means of acetanilides as amine components has been developed for the first time using copper catalysis. The approach is versatile and proceeds through sequential acylation and deacylation steps to afford benzanilides.

Graphical abstract: Copper catalysed C–N bond formation via a sequential acylation and deacylation process: a novel strategy for the synthesis of benzanilides

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Article information

DOI
https://doi.org/10.1039/C4RA15140B
Article type
Paper
Submitted
24 Nov 2014
Accepted
06 Jan 2015
First published
06 Jan 2015

RSC Adv., 2015,5, 9920-9924

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Copper catalysed C–N bond formation via a sequential acylation and deacylation process: a novel strategy for the synthesis of benzanilides

S. Kumar, R. Vanjari, T. Guntreddi and K. N. Singh, RSC Adv., 2015, 5, 9920 DOI: 10.1039/C4RA15140B

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