4.6 Article

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

Journal

ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 12, Issue 47, Pages 9631-9637

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c4ob01912a

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Funding

  1. Council of Scientific and Industrial Research (CSIR), New Delhi, India

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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.

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