Issue 46, 2015

Silver-catalyzed TEMPO oxidative homocoupling of indoles for the synthesis of 3,3′-biindolin-2-ones

Abstract

An oxidative homo dimerization of free indole derivatives, by means of silver catalysis and TEMPO oxidant, was first successful demonstrated. This new methodology is both atom and step efficient and is applicable to a broad scope of substrates, allowing the synthesis of a range of synthetically valuable substituted C3–C3′ bisindolin-2-ones in moderate to excellent yields.

Graphical abstract: Silver-catalyzed TEMPO oxidative homocoupling of indoles for the synthesis of 3,3′-biindolin-2-ones

Supplementary files

Article information

Article type
Communication
Submitted
08 Mar 2015
Accepted
13 Apr 2015
First published
13 Apr 2015

RSC Adv., 2015,5, 37018-37022

Silver-catalyzed TEMPO oxidative homocoupling of indoles for the synthesis of 3,3′-biindolin-2-ones

F. Lin, Y. Chen, B. Wang, W. Qin and L. Liu, RSC Adv., 2015, 5, 37018 DOI: 10.1039/C5RA04106F

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