Issue 6, 2017

Introducing tetramethylurea as a new methylene precursor: a microwave-assisted RuCl3-catalyzed cross dehydrogenative coupling approach to bis(indolyl)methanes

Abstract

Herein we report a microwave assisted Ru(III)/TBHP-mediated reaction of indoles with tetramethylurea (TMU) synthesizing symmetrical as well as unsymmetrical bis(indolyl)methanes, where TMU acts as a methylenating agent. This is the first report where TMU is used as a methylene source. Moreover, the synthesis of unsymmetrical bis(indolyl)methanes by using a carbon precursor is also reported herein for the first time. Various substituted indoles are used for the reaction. The reaction is high yielding and takes a much shorter time to accomplish compared to the existing methods.

Graphical abstract: Introducing tetramethylurea as a new methylene precursor: a microwave-assisted RuCl3-catalyzed cross dehydrogenative coupling approach to bis(indolyl)methanes

Supplementary files

Article information

Article type
Paper
Submitted
06 Dec 2016
Accepted
11 Jan 2017
First published
12 Jan 2017

Org. Biomol. Chem., 2017,15, 1435-1443

Introducing tetramethylurea as a new methylene precursor: a microwave-assisted RuCl3-catalyzed cross dehydrogenative coupling approach to bis(indolyl)methanes

M. L. Deb, P. J. Borpatra, P. J. Saikia and P. K. Baruah, Org. Biomol. Chem., 2017, 15, 1435 DOI: 10.1039/C6OB02671K

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