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dc.contributor.authorGeorge, S C-
dc.contributor.authorSreeja, T-
dc.contributor.authorAnas, S-
dc.contributor.authorRadhakrishnan, K V-
dc.contributor.authorYamamoto, Y-
dc.date.accessioned2013-11-13T06:23:40Z-
dc.date.available2013-11-13T06:23:40Z-
dc.date.issued2011-
dc.identifier.citationOrganic Letters 13(19):4984-4987;07 Oct 2011en_US
dc.identifier.issn1523-7060-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/737-
dc.description.abstractThe palladium catalyzed 1, 8-conjugate addition of heptafulvene, an antiaromatic conjugated 8 pi-electron system, is discussed. The method is utilized for the concise synthesis of bis-functionalized cycloheptatriene (CHT) derivatives. This is the first report on the palladium catalyzed bisfunctionalization of a cyclic cross conjugated system.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectActivated olefinsen_US
dc.subjectCycloaddition reactionsen_US
dc.subjectAlpha-allylationen_US
dc.subject8-Cyanoheptafulveneen_US
dc.subject8, 8-Dicyano-3-(4'-N, N-Dimethylamino) Phenylheptafulveneen_US
dc.subject1, 6-Additionen_US
dc.subjectBenzyneen_US
dc.titlePalladium catalyzed 1, 8-conjugate addition to heptafulvene via bis-pi-allyl palladium complexesen_US
dc.typeArticleen_US
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