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dc.contributor.authorSasikumar, P-
dc.contributor.authorPrabha, B-
dc.contributor.authorChand, S S-
dc.contributor.authorAswathy, M-
dc.contributor.authorMadhukrishnan, M-
dc.contributor.authorPreethanuj, P-
dc.contributor.authorSuresh, E-
dc.contributor.authorJaroschik, F-
dc.contributor.authorRadhakrishnan, K V-
dc.date.accessioned2018-06-21T05:52:26Z-
dc.date.available2018-06-21T05:52:26Z-
dc.date.issued2017-08-17-
dc.identifier.citationEuropean Journal of Organic Chemistry, 2017(30):4469-4474en_US
dc.identifier.urihttp://10.10.100.66:8080/xmlui/handle/123456789/3120-
dc.description.abstractA Lewis acid catalyzed double hydro(hetero)arylation of alkyl-substituted pentafulvenes for the synthesis of bisindolesubstituted cyclopentenoids has been developed. The scope of the reaction was explored with a wide range of indoles and pentafulvenes, and mechanistic insights were obtained. In addi-tion, we have also demonstrated a hydro(hetero)arylation–dehydroxylation reaction of 2-hydroxy-substituted pentafulvenes to afford bisindole derivatives with isoprenyl-substituted cyclopentene moieties.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectFulvenesen_US
dc.subjectC–C couplingen_US
dc.subjectHydro(hetero)arylationen_US
dc.subjectLewis acidsen_US
dc.subjectNitrogen heterocyclesen_US
dc.titleLewis Acid Promoted Regioselective Double Hydro(hetero)arylation of 6,6′-Dialkyl-Substituted Pentafulvenes: A Facile Approach to Bisindole Derivativesen_US
dc.typeArticleen_US
Appears in Collections:2017

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