Exploring Gold Catalysis in a 1,6-Conjugate Addition/Domino Electrophilic Cyclization Cascade: Synthesis of Cyclohepta[b]indoles

dc.contributor.authorJadhav, A.S.
dc.contributor.authorPankhade, Y.A.
dc.contributor.authorAnand, R.V.
dc.date.accessioned2020-11-19T10:11:16Z
dc.date.available2020-11-19T10:11:16Z
dc.date.issued2018
dc.description.abstractAn effective method for the construction of the structurally complex fused cyclohepta[b]indole core has been developed through an intermolecular 1,6-conjugate addition of indoles to 2-alkynyl p-quinone methides followed by an intramolecular electrophilic cyclization under oxophilic and alkynophilic gold catalysis.en_US
dc.identifier.citationJournal of Organic Chemistry, 83(15), pp. 8615-8626en_US
dc.identifier.otherhttps://doi.org/10.1021/acs.joc.8b00607
dc.identifier.urihttps://pubs.acs.org/doi/abs/10.1021/acs.joc.8b00607
dc.identifier.urihttp://hdl.handle.net/123456789/1914
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subject1 ,6-conjugate additionsen_US
dc.subjectElectrophilic cyclizationen_US
dc.subjectp-Quinone methidesen_US
dc.subjectCyclizationen_US
dc.subjectquinone derivativeen_US
dc.subjectelectrophilicityen_US
dc.titleExploring Gold Catalysis in a 1,6-Conjugate Addition/Domino Electrophilic Cyclization Cascade: Synthesis of Cyclohepta[b]indolesen_US
dc.typeArticleen_US

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