Issue 38, 2014

Oxidative cleavage of benzylic C–N bonds under metal-free conditions

Abstract

An interesting procedure for the oxidative cleavage of benzylic C–N bonds has been developed. Using TBAI as the catalyst and H2O2 as the oxidant, various benzylamines were transformed into their corresponding aromatic aldehydes in moderate to good yields. Notably, this is the first example of an oxidative cleavage of benzylic C–N bonds under metal-free conditions.

Graphical abstract: Oxidative cleavage of benzylic C–N bonds under metal-free conditions

Supplementary files

Article information

Article type
Communication
Submitted
30 Jul 2014
Accepted
12 Aug 2014
First published
12 Aug 2014

Org. Biomol. Chem., 2014,12, 7486-7488

Author version available

Oxidative cleavage of benzylic C–N bonds under metal-free conditions

J. Gong, X. Qi, D. Wei, J. Feng and X. Wu, Org. Biomol. Chem., 2014, 12, 7486 DOI: 10.1039/C4OB01633E

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