Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/1925
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dc.contributor.authorMishra, U.K.-
dc.contributor.authorYadav, Sonu-
dc.contributor.authorRamasastry, S.S.V.-
dc.date.accessioned2020-11-20T04:48:58Z-
dc.date.available2020-11-20T04:48:58Z-
dc.date.issued2017-
dc.identifier.citationJournal of Organic Chemistry, 82 (13)en_US
dc.identifier.other10.1021/acs.joc.7b00865-
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/acs.joc.7b00865-
dc.identifier.urihttp://hdl.handle.net/123456789/1925-
dc.description.abstractDiversity oriented one-pot synthesis of cyclohepta[b]indoles, indolotropones, and tetrahydrocarbazoles (THCs) have been reported. Readily accessible 3-(2-aminophenyl)-5-hexenyn-3-ols under a one-pot trimetallic orthogonal catalysis furnish tetrahydrocyclohepta[b]indoles, and a one-pot quadruple reaction sequence of the enynols generates dihydrocyclohepta[b]indoles and indolotropones. During this study, formation of THCs was realized to be a reason for the yield loss in certain cases, this observation led to the development of a one-pot bimetallic approach for the synthesis of 1,3-disubstituted THCs.en_US
dc.language.isoen_USen_US
dc.publisherACS Publicationsen_US
dc.subjectCatalystsen_US
dc.subjectIndolesen_US
dc.subjectCatalytic reactionsen_US
dc.subjectDiversity oriented synthesisen_US
dc.titleOne-Pot Multicatalytic Approaches for the Synthesis of Cyclohepta[b]indoles, Indolotropones, and Tetrahydrocarbazolesen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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