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dc.contributor.authorSana, Sravani
dc.contributor.authorReddy Dannarm, Srinivas
dc.contributor.authorTokala, Ramya
dc.contributor.authorDastari, Sowmya
dc.contributor.authorSathish, Manda
dc.contributor.authorKumar, Rahul
dc.contributor.authorSonti, Rajesh
dc.contributor.authorShankaraiah, Nagula
dc.date.accessioned2025-03-12T13:44:05Z
dc.date.available2025-03-12T13:44:05Z
dc.date.issued2023
dc.identifier.urihttp://repositorio.ucm.cl/handle/ucm/5845
dc.description.abstractA sustainable visible light-mediated synthetic protocol for the construction of color-tunable fluorescent 6-aryl-derived naphthoimidazo[1,2-a]pyridine- and anthraimidazo[1,2-a]pyridine-based molecules has been achieved via ruthenium-catalyzed sequential multiple C–H activation/annulation between heteroarenes and sulfoxonium ylides. This annulation strategy provides easy access to obtain a library of fused heterocyclic frameworks with significant yields and atom economy. In furthering this protocol to discover new small N-fused heterocyclic fluorophores, we also demonstrate a systematic investigation using a practical and computational analysis of photophysical properties. A conceptual trend is deep-rooted across a series of naphthyl and anthracene fused imidazo[1,2-a]pyridines based on the predicted emission wavelengths and theoretical concepts. Towards the end, we demonstrate an effective method to understand and synthesize color-tunable fluorophores under mild reaction conditions with a broad substrate scope.es_CL
dc.language.isoenes_CL
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 Chile*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
dc.sourceMayo Clinic Proceedings, 99(4), 564-577es_CL
dc.titleSustainable photocatalytic C-H annulation of heteroarenes with sulfoxonium ylides: synthesis and photophysical properties of fused imidazo[1,2-a]pyridine-based moleculeses_CL
dc.typeArticlees_CL
dc.ucm.indexacionScopuses_CL
dc.ucm.indexacionIsies_CL
dc.ucm.uripubs.rsc.org/en/content/articlelanding/2023/QO/D3QO00923Hes_CL
dc.ucm.doidoi.org/10.1039/D3QO00923Hes_CL


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Atribución-NoComercial-SinDerivadas 3.0 Chile
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