Issue 1, 2018

Aerobic oxidative acylation of nitroarenes with arylacetic esters under mild conditions: facile access to diarylketones

Abstract

A facile and regioselective base-mediated aerobic oxidative acylation of nitroarenes to access diarylketones under mild conditions has been developed. It features the use of bench-stable and readily available arylacetates as acyl surrogates, and the absence of transition-metals and synthetic oxidants. This protocol involves a cascade CDC/oxidative decarboxylation process.

Graphical abstract: Aerobic oxidative acylation of nitroarenes with arylacetic esters under mild conditions: facile access to diarylketones

Supplementary files

Article information

Article type
Paper
Submitted
21 Nov 2017
Accepted
01 Dec 2017
First published
01 Dec 2017

Org. Biomol. Chem., 2018,16, 140-145

Aerobic oxidative acylation of nitroarenes with arylacetic esters under mild conditions: facile access to diarylketones

J. Li, Q. Yang, F. Yang, G. Chen, Z. Li, Y. Kuang, W. Zhang and P. Huang, Org. Biomol. Chem., 2018, 16, 140 DOI: 10.1039/C7OB02865B

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements