Pentafluorobenzoic Acid Catalyzed 1,6-Conjugate Addition of Indoles to p-Quinone Methides

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dc.contributor.authorChowdhury, Arjun.
dc.date.accessioned2021-09-14T07:02:20Z
dc.date.available2021-09-14T07:02:20Z
dc.date.issued2021-07-28
dc.description.abstractPentafluorobenzoic acid has been utilized as a non-covalent Br Ø nsted acid catalyst for the 1,6- conjugate addition of indoles to para-quinone methides. This transformation tolerant to a variety of functional groups and occurs in mild conditions. This methodology provides an easy and straightforward access to a set of unsymmetrical diarylindolylmethanes in moderate to good yields.en_US
dc.guideAnand, R.V.
dc.identifier.urihttp://hdl.handle.net/123456789/3864
dc.language.isoenen_US
dc.publisherIISERMen_US
dc.subjectPentafluorobenzoicen_US
dc.subjectp-Quinoneen_US
dc.subjectMethidesen_US
dc.titlePentafluorobenzoic Acid Catalyzed 1,6-Conjugate Addition of Indoles to p-Quinone Methidesen_US
dc.typeThesisen_US

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