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Lewis Acid Catalyzed Annulation of Cyclopropane Carbaldehydes and Aryl Hydrazines: Construction of tetrahydropyridazines and application toward a one-pot synthesis of hexahydropyrrolo[1,2- b]pyridazines

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dc.contributor.author Dey, R.
dc.contributor.author Kumar, P.
dc.contributor.author Banerjee, P.
dc.date.accessioned 2018-10-05T08:48:34Z
dc.date.available 2018-10-05T08:48:34Z
dc.date.issued 2018-10-05
dc.identifier.uri http://localhost:8080/xmlui/handle/123456789/975
dc.description.abstract In 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.iso en_US en_US
dc.title Lewis Acid Catalyzed Annulation of Cyclopropane Carbaldehydes and Aryl Hydrazines: Construction of tetrahydropyridazines and application toward a one-pot synthesis of hexahydropyrrolo[1,2- b]pyridazines en_US
dc.type Article en_US


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