Issue 14, 2016

A general metal-free route towards the synthesis of 1,2,3-triazoles from readily available primary amines and ketones

Abstract

An unprecedented approach that enables the direct and selective preparation of 1,5-disubstituted 1,2,3-triazoles from abundantly available building blocks such as primary amines, enolizable ketones and 4-nitrophenyl azide as a renewable source of dinitrogen via an organocascade process has been developed. Furthermore, this efficient methodology also enables the synthesis of fully functionalized and fused N-substituted heterocycles.

Graphical abstract: A general metal-free route towards the synthesis of 1,2,3-triazoles from readily available primary amines and ketones

Supplementary files

Article information

Article type
Communication
Submitted
14 Oct 2015
Accepted
23 Dec 2015
First published
23 Dec 2015

Chem. Commun., 2016,52, 2885-2888

Author version available

A general metal-free route towards the synthesis of 1,2,3-triazoles from readily available primary amines and ketones

J. Thomas, S. Jana, J. John, S. Liekens and W. Dehaen, Chem. Commun., 2016, 52, 2885 DOI: 10.1039/C5CC08347H

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