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Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2337
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dc.contributor.authorMaiti, Dhriti-
dc.date.accessioned2024-04-03T15:47:12Z-
dc.date.available2024-04-03T15:47:12Z-
dc.date.issued2023-05-
dc.identifier.urihttp://hdl.handle.net/123456789/2337-
dc.descriptionEmbargo Perioden_US
dc.description.abstractTropylium tetrafluoroborate has been utilized as a Lewis acid promoter for the 1,6-conjugate addition of 2-Naphthol to para-quinone methides. This work demonstrates a transformation which occurs at mild conditions and is tolerable to many different functional groups. This protocol provides an easy and straightforward access to a set of unsymmetrical diarylnaphthol methanes in good to excellent yield.en_US
dc.language.isoenen_US
dc.publisherIISER Mohalien_US
dc.subjectp-quinone methidesen_US
dc.subjectAromatic ionsen_US
dc.titleTropylium Tetrafluoroborate Catalyzed 1,6-Conjugate Addition of 2-Naphthol to p-Quinone Methidesen_US
dc.typeThesisen_US
dc.guideAnand, Vijaya Ren_US
Appears in Collections:MS-18

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