Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/17311
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dc.contributor.authorSurve, Shivaji V.en_US
dc.contributor.authorBhawale, Rajesh T.en_US
dc.contributor.authorBiswas, Biswajiten_US
dc.contributor.authorKshirsagar, Umesh A.en_US
dc.date.accessioned2025-12-04T10:00:51Z-
dc.date.available2025-12-04T10:00:51Z-
dc.date.issued2025-
dc.identifier.citationSurve, Shivaji V., Bhawale, R. T., Biswas, B., & Kshirsagar, U. A. (2025). Palladium-Catalyzed Photoinduced Regioselective C8 Arylation of 1-(Pyridin-2-yl)quinolin-4(1H)-Ones with Aryl Diazonium Salts. European Journal of Organic Chemistry. https://doi.org/10.1002/ejoc.202500961en_US
dc.identifier.issn1434-193X-
dc.identifier.issn1099-0690-
dc.identifier.otherEID(2-s2.0-105022738398)-
dc.identifier.urihttps://dx.doi.org/10.1002/ejoc.202500961-
dc.identifier.urihttps://dspace.iiti.ac.in:8080/jspui/handle/123456789/17311-
dc.description.abstractA visible-light-mediated regioselective C8 arylation of quinolinones has been developed by merging transition-metal catalysis with photoredox catalysis. This approach offers broad substrate scope and mild reaction conditions, affording the desired products in up to 85% yield. Furthermore, to investigate the reaction mechanism, several control experiments were performed, including fluorescence quenching studies, quantum yield measurements, light-on/off experiments, kinetic isotope effect (KIE) analysis, and H/D labeling experiments. This strategy exhibits excellent scalability and also enables subsequent C2 alkenylation. © 2025 Wiley-VCH GmbH.en_US
dc.language.isoenen_US
dc.publisherJohn Wiley and Sons Incen_US
dc.sourceEuropean Journal of Organic Chemistryen_US
dc.subjectaryl diazonium salten_US
dc.subjectarylationen_US
dc.subjectdual catalysisen_US
dc.subjectheterocyclesen_US
dc.subjectquinolinoneen_US
dc.titlePalladium-Catalyzed Photoinduced Regioselective C8 Arylation of 1-(Pyridin-2-yl)quinolin-4(1H)-Ones with Aryl Diazonium Saltsen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

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