Issue 6, 2017

[3+2] Cycloaddition of azide with aldehyde hydrazone through an aminyl radical-polar crossover strategy

Abstract

A novel approach to obtain functionalized tetrazoles by a [3+2] cycloaddition of azide with aldehyde hydrazone is reported. This reaction features a broad substrate scope and mild reaction conditions through an aminyl radical-polar crossover strategy.

Graphical abstract: [3+2] Cycloaddition of azide with aldehyde hydrazone through an aminyl radical-polar crossover strategy

Supplementary files

Article information

Article type
Communication
Submitted
02 Nov 2016
Accepted
17 Dec 2016
First published
19 Dec 2016

Chem. Commun., 2017,53, 1045-1047

[3+2] Cycloaddition of azide with aldehyde hydrazone through an aminyl radical-polar crossover strategy

Z. Wu, P. Xu, N. Zhou, Y. Duan, M. Zhang and C. Zhu, Chem. Commun., 2017, 53, 1045 DOI: 10.1039/C6CC08779E

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