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dc.contributor.authorAjesh, V-
dc.contributor.authorBaiju, T V-
dc.contributor.authorVarughese, S-
dc.contributor.authorRadhakrishnan, K V-
dc.date.accessioned2017-03-06T10:21:36Z-
dc.date.available2017-03-06T10:21:36Z-
dc.date.issued2016-07-06-
dc.identifier.citationTetrahedron Letters, 57(27-28):2965-2968en_US
dc.identifier.issn0040-4039-
dc.identifier.urihttp://hdl.handle.net/123456789/2700-
dc.description.abstractA facile route towards the synthesis of cyclopentene fused chromene derivatives from strained phenol substituted fulvene derived bicyclic hydrazines is described. The reaction is proceeding through base catalyzed sequential intramolecular ring opening and ring closure of azabicyclic olefins. The transition metal free method provides an easy access to biologically relevant fused chromene ring system under relatively mild reaction conditions.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subject2H-Chromeneen_US
dc.subjectBase catalyzeden_US
dc.subjectPentafulveneen_US
dc.subjectDiazabicyclic olefinen_US
dc.subjectElectrocyclic ring closureen_US
dc.titleTransition Metal Free Intramolecular Approach for the Synthesis of Cyclopenta[b]chromene Derivatives From Phenol Substituted Fulvene Derived Azabicyclic Olefinsen_US
dc.typeArticleen_US
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