Issue 29, 2018, Issue in Progress

Copper-catalyzed C–H acyloxylation of 2-phenylpyridine using oxygen as the oxidant

Abstract

An efficient copper-catalyzed direct o-acyloxylation of 2-phenylpyridine with carboxylic acids using oxygen as the oxidant has been developed. Various acids including aromatic acids, cinnamic acids and aliphatic acids are effective acyloxylation reagents and provide the desired products in moderate to excellent yields. The reaction proceeds well under an oxygen atmosphere, making this method potentially practical.

Graphical abstract: Copper-catalyzed C–H acyloxylation of 2-phenylpyridine using oxygen as the oxidant

Supplementary files

Article information

Article type
Paper
Submitted
06 Mar 2018
Accepted
27 Apr 2018
First published
03 May 2018
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2018,8, 16378-16382

Copper-catalyzed C–H acyloxylation of 2-phenylpyridine using oxygen as the oxidant

F. Wang, Z. Lin, W. Yu, Q. Hu, C. Shu and W. Zhang, RSC Adv., 2018, 8, 16378 DOI: 10.1039/C8RA01974F

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