Published in

Facultad de Humanidades y Ciencias de la Educación, Synthesis: Journal of Synthetic Organic Chemistry, 04(51), p. 921-932, 2018

DOI: 10.1055/s-0037-1610664

Links

Tools

Export citation

Search in Google Scholar

Catalyst-Free, Metal-Free, and Chemoselective Transamidation of Activated Secondary Amides

Journal article published in 2018 by Srinivasan Chandrasekaran ORCID, Rajagopal Ramkumar
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

Full text: Download

Red circle
Preprint: archiving forbidden
Green circle
Postprint: archiving allowed
Green circle
Published version: archiving allowed
Data provided by SHERPA/RoMEO

Abstract

A simple protocol, which is catalyst-free, metal-free, and chemoselective, for transamidation of activated secondary amides in ethanol as solvent under mild conditions is reported. A wide range of amines, amino acids, amino alcohols, and the substituents, which are problematic in catalyzed transamidation, are tolerated in this methodology. The transamidation reaction was successfully extended to water as the medium as well. The present methodology appears to be better than the other catalyzed transamidations reported recently.