Cycloprenium Ion Catalyzed 1,6-Conjugate Addition of Indoles to p-Quinone Methides

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dc.contributor.authorNandy, Arkopal
dc.date.accessioned2024-02-06T05:03:33Z
dc.date.available2024-02-06T05:03:33Z
dc.date.issued2023-05
dc.descriptionembargo perioden_US
dc.description.abstractCyclopropenium salt has been used as a Lewis-Acid organocatalyst for performing 1,6 Conjugate Addition of Indoles to p-Quinone Methide systems. The reaction progresses efficiently at room temperatures with rapid reaction times thereby, constructing the biologically important diarylindolylmethanes in good to excellent yields.en_US
dc.guideAnand, R Vijayaen_US
dc.identifier.urihttp://hdl.handle.net/123456789/5376
dc.language.isoenen_US
dc.publisherIISER Mohalien_US
dc.subjectCyclopreniumen_US
dc.subjectCatalyzeden_US
dc.subjectp-Quinoneen_US
dc.titleCycloprenium Ion Catalyzed 1,6-Conjugate Addition of Indoles to p-Quinone Methidesen_US
dc.typeThesisen_US

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