Issue 26, 2014

TEMPO-mediated allylic C–H amination with hydrazones

Abstract

TEMPO-mediated reactions of alkenyl hydrazones afforded azaheterocycles via sp3 C–H allylic amination. The transformation is featured by a sequence of remote allylic H-radical shift and allylic homolytic substitution with hydrazone radicals.

Graphical abstract: TEMPO-mediated allylic C–H amination with hydrazones

Supplementary files

Article information

Article type
Communication
Submitted
23 Apr 2014
Accepted
10 May 2014
First published
13 May 2014

Org. Biomol. Chem., 2014,12, 4567-4570

Author version available

TEMPO-mediated allylic C–H amination with hydrazones

X. Zhu and S. Chiba, Org. Biomol. Chem., 2014, 12, 4567 DOI: 10.1039/C4OB00839A

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