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

dc.contributor.authorDhiman, Seema
dc.contributor.authorRamasastry, S.S.V.
dc.date.accessioned2020-12-11T06:05:41Z
dc.date.available2020-12-11T06:05:41Z
dc.date.issued2015
dc.description.abstractAn 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.identifier.citationChemical Communications, 51(3) pp. 557-560.en_US
dc.identifier.other10.1039/c4cc08174a
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2015/cc/c4cc08174a#!divAbstract
dc.identifier.urihttp://hdl.handle.net/123456789/3020
dc.language.isoen_USen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectSynthesisen_US
dc.subjectpolysubstituted cyclopenta[b]en_US
dc.subjectgold(i)/Brønsted aciden_US
dc.titleSynthesis of polysubstituted cyclopenta[b]indoles via relay gold(i)/Brønsted acid catalysisen_US
dc.typeArticleen_US

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