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

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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. This journal is

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Dhiman, S., & Ramasastry, S. S. V. (2015). Synthesis of polysubstituted cyclopenta[b]indoles via relay gold(i)/Brønsted acid catalysis. Chemical Communications, 51(3), 557–560. https://doi.org/10.1039/c4cc08174a

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