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

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DC Field	Value	Language
dc.contributor.author	Dhiman, Seema	-
dc.contributor.author	Ramasastry, S.S.V.	-
dc.date.accessioned	2020-12-11T06:05:41Z	-
dc.date.available	2020-12-11T06:05:41Z	-
dc.date.issued	2015	-
dc.identifier.citation	Chemical Communications, 51(3) pp. 557-560.	en_US
dc.identifier.other	10.1039/c4cc08174a	-
dc.identifier.uri	https://pubs.rsc.org/en/content/articlelanding/2015/cc/c4cc08174a#!divAbstract	-
dc.identifier.uri	http://hdl.handle.net/123456789/3020	-
dc.description.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.	en_US
dc.language.iso	en_US	en_US
dc.publisher	Royal Society of Chemistry	en_US
dc.subject	Synthesis	en_US
dc.subject	polysubstituted cyclopenta[b]	en_US
dc.subject	gold(i)/Brønsted acid	en_US
dc.title	Synthesis of polysubstituted cyclopenta[b]indoles via relay gold(i)/Brønsted acid catalysis	en_US
dc.type	Article	en_US
Appears in Collections:	Research Articles

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