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DC Field | Value | Language |
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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 |
Appears in Collections: | Year-2018 |
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Full Text.pdf | 1.1 MB | Adobe PDF | View/Open Request a copy |
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