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dc.contributor.authorDey, R.-
dc.contributor.authorKumar, P.-
dc.contributor.authorBanerjee, P.-
dc.date.accessioned2018-10-05T08:48:34Z-
dc.date.available2018-10-05T08:48:34Z-
dc.date.issued2018-10-05-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/975-
dc.description.abstractIn this report, a facile synthesis of tetrahydropyridazines via a Lewis acid catalyzed annulation reaction of cyclopropane carbaldehydes and aryl hydrazines has been demonstrated. Moreover, the generated tetrahydropyridazine further participated in a cycloaddition reaction with donor−acceptor cyclopropanes to furnish hexahydropyrrolo[1,2-b]pyridazines. We also performed these two steps in one pot in a consecutive manner. In addition, a monodecarboxylation reaction of hexahydropyrrolo[1,2-b]pyridazine was achieved with a good yield.en_US
dc.language.isoen_USen_US
dc.titleLewis Acid Catalyzed Annulation of Cyclopropane Carbaldehydes and Aryl Hydrazines: Construction of tetrahydropyridazines and application toward a one-pot synthesis of hexahydropyrrolo[1,2- b]pyridazinesen_US
dc.typeArticleen_US
Appears in Collections:Year-2018

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