Issue 95, 2014

Silver-catalyzed tandem radical acylarylation of cinnamamides in aqueous media

Abstract

A mild silver-catalyzed regioselective radical addition/cyclization reaction of cinnamamides with α-oxocarboxylic acids has been developed. The procedure proceeded well under very mild conditions, leading to a diverse range of 3-acyl-4-aryldihydroquinolin-2(1H)-ones in moderate to good yields.

Graphical abstract: Silver-catalyzed tandem radical acylarylation of cinnamamides in aqueous media

Supplementary files

Article information

Article type
Paper
Submitted
12 Aug 2014
Accepted
30 Sep 2014
First published
02 Oct 2014

RSC Adv., 2014,4, 52986-52990

Silver-catalyzed tandem radical acylarylation of cinnamamides in aqueous media

H. Yang, L. Guo and X. Duan, RSC Adv., 2014, 4, 52986 DOI: 10.1039/C4RA08529A

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