Issue 3, 2015

Synthesis of polysubstituted cyclopenta[b]indoles via relay gold(i)/Brønsted acid catalysis

Abstract

An efficient relay catalytic process involving Au(I)/Brønsted acid to access various polysubstituted cyclopentannulated indoles from easily accessible 1-(2-aminophenyl)prop-2-ynols and readily available 1,3-dicarbonyls has been developed. In an unprecedented event, the intermediate 2-indolylmethyl cations undergo the cation-Ene reaction with various 1,3-dicarbonyls followed by an intramolecular Friedel–Crafts-type reaction generating functionalized cyclopenta[b]indoles.

Graphical abstract: Synthesis of polysubstituted cyclopenta[b]indoles via relay gold(i)/Brønsted acid catalysis

Supplementary files

Article information

Article type
Communication
Submitted
15 Oct 2014
Accepted
06 Nov 2014
First published
06 Nov 2014
This article is Open Access
Creative Commons BY-NC license

Chem. Commun., 2015,51, 557-560

Synthesis of polysubstituted cyclopenta[b]indoles via relay gold(I)/Brønsted acid catalysis

S. Dhiman and S. S. V. Ramasastry, Chem. Commun., 2015, 51, 557 DOI: 10.1039/C4CC08174A

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