Issue 47, 2014

Copper catalyzed oxidative ortho-C–H benzoxylation of 2-phenylpyridines with benzyl alcohols and benzyl amines as benzoxylation sources

Abstract

A simple and efficient protocol for the oxidative ortho benzoxylation of 2-phenylpyridines with benzyl alcohols and benzyl amines via C–H bond activation has been developed. The present protocol uses benzyl alcohol and benzyl amine as inexpensive and easily available starting materials to afford benzoxylation products in moderate to good yields in the presence of the Cu/TBHP catalytic system.

Graphical abstract: Copper catalyzed oxidative ortho-C–H benzoxylation of 2-phenylpyridines with benzyl alcohols and benzyl amines as benzoxylation sources

Supplementary files

Article information

Article type
Paper
Submitted
09 Sep 2014
Accepted
01 Oct 2014
First published
01 Oct 2014

Org. Biomol. Chem., 2014,12, 9631-9637

Author version available

Copper catalyzed oxidative ortho-C–H benzoxylation of 2-phenylpyridines with benzyl alcohols and benzyl amines as benzoxylation sources

A. B. Khemnar and B. M. Bhanage, Org. Biomol. Chem., 2014, 12, 9631 DOI: 10.1039/C4OB01912A

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