Issue 36, 2014

A facile manganese dioxide mediated oxidation of primary benzylamines to benzamides

Abstract

A high yielding manganese dioxide mediated oxidation of benzylamines to the corresponding amides has been developed under mild reaction conditions. The mechanism for the conversion has been explored by 1H NMR spectroscopy and the role of both manganese dioxide and molecular sieves in the reaction elucidated.

Graphical abstract: A facile manganese dioxide mediated oxidation of primary benzylamines to benzamides

Supplementary files

Article information

Article type
Paper
Submitted
05 Jun 2014
Accepted
29 Jul 2014
First published
30 Jul 2014

Org. Biomol. Chem., 2014,12, 7150-7158

Author version available

A facile manganese dioxide mediated oxidation of primary benzylamines to benzamides

A. Poeschl and D. M. Mountford, Org. Biomol. Chem., 2014, 12, 7150 DOI: 10.1039/C4OB01166J

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