Issue 82, 2014

Copper-catalyzed tandem annulation/arylation for the synthesis of diindolylmethanes from propargylic alcohols

Abstract

Various highly substituted 2,3′-diindolylmethane heterocycles were prepared from propargylic alcohols and indole nucleophiles via a transition metal-catalyzed tandem indole annulation/arylation reaction for the first time. Among the metal catalysts we examined, the most economical copper(I) catalyst provided the highest efficiency. The indole nucleophiles could also be replaced by other electron-rich arenes or alcohols.

Graphical abstract: Copper-catalyzed tandem annulation/arylation for the synthesis of diindolylmethanes from propargylic alcohols

Supplementary files

Article information

Article type
Communication
Submitted
29 Jul 2014
Accepted
25 Aug 2014
First published
02 Sep 2014

Chem. Commun., 2014,50, 12293-12296

Copper-catalyzed tandem annulation/arylation for the synthesis of diindolylmethanes from propargylic alcohols

H. Li, X. Li, H. Wang, G. N. Winston-McPherson, H. J. Geng, I. A. Guzei and W. Tang, Chem. Commun., 2014, 50, 12293 DOI: 10.1039/C4CC05901H

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