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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/2806
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dc.contributor.authorKumar, Anil-
dc.date.accessioned2021-10-14T13:09:24Z-
dc.date.available2021-10-14T13:09:24Z-
dc.date.issued2021-
dc.identifier.urihttps://pubs.acs.org/doi/abs/10.1021/acs.orglett.1c00031-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2806-
dc.description.abstractA simple and highly efficient metal-free method has been developed for hydroxyfluoroalkylation of indoles and imidazo[1,2-a]pyridines via TEMPO-mediated C(sp3)–H and C(sp2)–H bond cross-dehydrogenative coupling of fluorinated alcohols and indoles. The protocol showed broad substrate scope, afforded good yields of hydroxyfluoroalkylated products, and was amenable for scale-up. Mechanistic investigation indicated involvement of the radical pathway.en_US
dc.language.isoenen_US
dc.publisherACSen_US
dc.subjectChemistryen_US
dc.subjectFunctionalizationen_US
dc.subjectIndolesen_US
dc.subjectChemical reactionsen_US
dc.titleTEMPO-Mediated Cross-Dehydrogenative Coupling of Indoles and Imidazo[1,2-a]pyridines with Fluorinated Alcoholsen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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