Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/4541
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dc.contributor.authorRekha-
dc.contributor.authorSharma, Sonam-
dc.contributor.authorAnand, Ramasamy Vijaya-
dc.date.accessioned2023-08-11T13:10:04Z-
dc.date.available2023-08-11T13:10:04Z-
dc.date.issued2022-
dc.identifier.citationEuropean Journal of Organic Chemistry, 2022(46), 2201323en_US
dc.identifier.urihttps://doi.org/10.1002/ejoc.202201323-
dc.identifier.urihttp://hdl.handle.net/123456789/4541-
dc.descriptionOnly IISER Mohali authors are available in the recorden_US
dc.description.abstractIn this article, we demonstrate an atom economical, practical, mild and selective HBF4-catalyzed 1,6-conjugate addition of carbazoles to para-Quinone Methides (p-QMs) to access 3,6-bis-diarylmethyl- and mono-diarylmethyl carbazoles. This metal and additive free protocol provides convenient access to the substituted carbazole derivatives in moderate to excellent yields with a good functional group tolerance. It was found that a couple of 3,6-disubstituted carbazoles showed interesting photophysical properties and, therefore, might potentially find some applications as host materials in OLEDs.en_US
dc.language.isoen_USen_US
dc.publisherChemistry Europeen_US
dc.subjectCarbazolesen_US
dc.subjectpara-Quinone Methidesen_US
dc.titleHBF4-Catalyzed 3,6-Bis-diarylmethylation of Carbazoles with para-Quinone Methidesen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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