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dc.contributor.authorVerma, K.-
dc.contributor.authorBanerjee, P.-
dc.date.accessioned2017-12-21T11:25:00Z-
dc.date.available2017-12-21T11:25:00Z-
dc.date.issued2017-12-21-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/874-
dc.description.abstractLewis acid catalyzed formal [3+2] cycloadditions of 1-azadienes with donor acceptor cyclopropanes to synthesize varieties of imine functionalized cyclopentanes and pyrrolidine derivatives in moderate to high yield have been developed. Moreover, pharmaceutically relevant azabicyclo[3.2.1] octane, bearing two all-carbon quaternary stereogenic centers at the bridgehead positions, has been synthesized by nosyl group deprotection and intramolecular amidation of imine functionalized cyclopentane derivative.en_US
dc.language.isoen_USen_US
dc.subjectDonor-Acceptor Cyclopropaneen_US
dc.subject1-Azadienesen_US
dc.subjectImine Functionalized Cyclopentanesen_US
dc.subjectPyrrolidineen_US
dc.subjectazabicyclo[3.2.1]octaneen_US
dc.titleLewis acid catalyzed formal [3+2] cycloaddition of donor-acceptor cyclopropanes and 1-Azadienes: synthesis of imine functionalized cyclopentanes and pyrrolidine derivativesen_US
dc.typeArticleen_US
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