Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2068
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dc.contributor.authorYadav, S.-
dc.contributor.authorHazra, R.-
dc.contributor.authorSingh, Animesh-
dc.contributor.authorRamasastry, S.S.V.-
dc.date.accessioned2020-11-23T11:22:49Z-
dc.date.available2020-11-23T11:22:49Z-
dc.date.issued2019-
dc.identifier.citationOrganic Letters, 21(9),pp.2983-2987.en_US
dc.identifier.otherhttps://doi.org/10.1021/acs.orglett.9b00410-
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/acs.orglett.9b00410-
dc.identifier.urihttp://hdl.handle.net/123456789/2068-
dc.description.abstractAn efficient palladium-catalyzed intramolecular Trost–Oppolzer type Alder-ene strategy was developed for the synthesis of carbazoles and cyclopenta[b]indoles from easily accessible(3-allyl-1H-indol-2-yl)methyl acetates. This strategy was extended for the synthesis of naphthalenes and dibenzobenzofurans as well. In addition, a short synthesis of antibacterial and antifungal natural product glycozoline and its analogues was also achieved.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectIntramolecularen_US
dc.subjectTrost–Oppolzeren_US
dc.subjectAntifungalen_US
dc.subjectNaturalen_US
dc.titleSubstituent-Guided Palladium-Ene Reaction for the Synthesis of Carbazoles and Cyclopenta[b]indolesen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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