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Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/1161
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dc.contributor.authorKumar, Suresh-
dc.date.accessioned2019-11-21T10:26:14Z-
dc.date.available2019-11-21T10:26:14Z-
dc.date.issued2019-11-21-
dc.identifier.urihttp://hdl.handle.net/123456789/1161-
dc.description.abstractTropylium tetrafluoroboratehas been utilized as a BrØnsted base for the 1,6-conjugate addition of indoles to para-quinone methides. This transformation occurs at mild conditions and is tolerant to a variety of functional groups. This protocol provides an easy and straightforward access to a set of unsymmetrical diarylindolylmethanes in good to excellent yield.en_US
dc.language.isoen_USen_US
dc.publisherIISERMen_US
dc.subjectTropylium tetrafluoroboratehasen_US
dc.subjectQuinone methidesen_US
dc.subjectFunctional groupsen_US
dc.subjectDiarylindolylmethanesen_US
dc.titleTropylium Tetrafluoroborate Catalyzed 1,6-Conjugate Addition of Indoles to p-Quinone Methidesen_US
dc.typeThesisen_US
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