Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/14082
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dc.contributor.advisorSamanta, Sampak-
dc.contributor.authorKushwah, Shishupal-
dc.date.accessioned2024-07-29T10:21:58Z-
dc.date.available2024-07-29T10:21:58Z-
dc.date.issued2024-05-10-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/14082-
dc.description.abstractA series of N-cyclopropyl pyrazole derivatives were synthesized in good to high yield. This reaction proceeds through an aza-Michael reaction between in situ generated cyclopropenecarboxylates as Michael acceptors and pyrazoles as Michael donors in the presence of base under heating conditions. Notably, this method is simple and has a good substrate scope.en_US
dc.language.isoenen_US
dc.publisherDepartment of Chemistry, IIT Indoreen_US
dc.relation.ispartofseriesMS443;-
dc.subjectChemistryen_US
dc.titleBase promoted Aza-Michael addition of pyrazole to 1-chlorocyclopropanecarboxylatesen_US
dc.typeThesis_M.Scen_US
Appears in Collections:Department of Chemistry_ETD

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