Issue 46, 2012

Dibenzo[a,c]carbazoles from 2-(2-bromoaryl)-3-arylindoles via a palladium-catalyzed intramolecular C–H functionalization/C–C bond formation process

Abstract

The palladium-catalyzed cyclization of 2-(2-bromoaryl)-3-arylindoles provides a new versatile approach to dibenzo[a,c]carbazoles. The reaction tolerates a variety of useful substituents including chloro, nitro, ether, cyano, keto, and ester groups.

Graphical abstract: Dibenzo[a,c]carbazoles from 2-(2-bromoaryl)-3-arylindoles via a palladium-catalyzed intramolecular C–H functionalization/C–C bond formation process

Supplementary files

Article information

Article type
Communication
Submitted
05 Sep 2012
Accepted
27 Sep 2012
First published
01 Oct 2012

Org. Biomol. Chem., 2012,10, 9142-9147

Dibenzo[a,c]carbazoles from 2-(2-bromoaryl)-3-arylindoles via a palladium-catalyzed intramolecular C–H functionalization/C–C bond formation process

S. Cacchi, G. Fabrizi, A. Goggiamani and A. Iazzetti, Org. Biomol. Chem., 2012, 10, 9142 DOI: 10.1039/C2OB26741A

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