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dc.contributor.authorJijy, E-
dc.contributor.authorPraveen, P-
dc.contributor.authorShimi, M-
dc.contributor.authorPihko, P M-
dc.contributor.authorNayana Joseph-
dc.contributor.authorRadhakrishnan, K V-
dc.date.accessioned2013-09-26T09:11:50Z-
dc.date.available2013-09-26T09:11:50Z-
dc.date.issued2013-
dc.identifier.citationChemical Communications 49(66):7349-7351; 2013en_US
dc.identifier.urihttp://hdl.handle.net/123456789/620-
dc.description.abstractAn efficient one pot strategy for the synthesis of cyclopentene fused chromanone derivatives through the direct oxidative coupling of salicylaldehydes with bicyclic olefins in the presence of a rhodium-copper catalyst system is described. This is the first report on the ring opening-ring closing of bicyclic hydrazines via metal catalyzed oxidative coupling reaction.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectMeso bicyclic hydrazinesen_US
dc.subjectEnantioselective desymmetrizationen_US
dc.subjectIntermolecular hydroacylationen_US
dc.subjectStereoselective-synthesisen_US
dc.subjectReagentsen_US
dc.subjectCyclopentannulationen_US
dc.subjectTransformationsen_US
dc.subjectCyclopentenesen_US
dc.subjectAnnulationen_US
dc.subjectalkenesen_US
dc.titleRhodium catalyzed oxidative coupling of salicylaldehydes with diazabicyclic olefins: a one pot strategy involving aldehyde C-H cleavage and pi-allyl chemistry towards the synthesis of fused ring chromanonesen_US
dc.typeArticleen_US
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