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dc.contributor.authorSarath Chand, S-
dc.contributor.authorJijy, E-
dc.contributor.authorPraveen, P-
dc.contributor.authorSzymoniak, J-
dc.contributor.authorPreethanuj, P-
dc.contributor.authorDhanya, B P-
dc.contributor.authorRadhakrishnan, K V-
dc.identifier.citationOrganic Letters 15(13): 3338-3341; 5 Jul 2013en_US
dc.description.abstractA palladium/Lewis acid mediated stepwise and one-pot transformation of pentafulvene derived diazabicyclic olefins is described. The reaction offers a facile strategy for the synthesis of novel spiropentacyclic motifs with indoline and pyrazolidine fused to the cyclopentene core.en_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectMeso-bicyclic hydrazinesen_US
dc.subjectFunctionalized cyclopentenesen_US
dc.subjectTrialkylaluminum reagentsen_US
dc.subjectCycloaddition reactionsen_US
dc.subjectFacile synthesisen_US
dc.titlePalladium/Lewis acid mediated domino reaction of pentafulvene derived diazabicyclic olefins: efficient access to spiropentacyclic motif with an indoline and pyrazolidine fused to cyclopenteneen_US
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