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Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2316
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dc.contributor.authorSaini, Piyush-
dc.date.accessioned2024-04-03T09:56:48Z-
dc.date.available2024-04-03T09:56:48Z-
dc.date.issued2023-05-
dc.identifier.urihttp://hdl.handle.net/123456789/2316-
dc.descriptionunder embargo perioden_US
dc.description.abstractCyclopropenium ion salt has been utilized as a Lewis acid for the 1,6-conjugate hydroolefinaton of alkenes to para-quinone methides via intramolecular and intermolecular fashion. This transformation requires mild conditions and applies to various functional groups. This protocol provides easy access to indene and vinyl diarylmethane derivatives in medium to excellent yields.en_US
dc.language.isoenen_US
dc.publisherIISER Mohalien_US
dc.subjectChemistryen_US
dc.subjectTris-arylcyclopropeniumen_US
dc.titleTris-arylcyclopropenium Carbocation Catalyzed Inter and Inter-molecular Hydroolefination Reactionsen_US
dc.typeThesisen_US
dc.guideAnand, R. Vijayaen_US
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