Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/16399
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dc.contributor.authorKirwale, Amol Bhivraoen_US
dc.contributor.authorBhawale, Rajesh T.en_US
dc.contributor.authorKshirsagar, Umesh Achyutraoen_US
dc.date.accessioned2025-07-09T13:48:00Z-
dc.date.available2025-07-09T13:48:00Z-
dc.date.issued2025-
dc.identifier.citationKirwale, A. B., Bhawale, R. T., & Kshirsagar, U. A. (2025). Visible-Light-Mediated Dual Catalytic Spiro Annulation of 2-Aryl Quinazolin-4(3H)-ones with N-Substituted Maleimides. European Journal of Organic Chemistry. https://doi.org/10.1002/ejoc.202500462en_US
dc.identifier.issn1434-193X-
dc.identifier.otherEID(2-s2.0-105008537564)-
dc.identifier.urihttps://dx.doi.org/10.1002/ejoc.202500462-
dc.identifier.urihttps://dspace.iiti.ac.in:8080/jspui/handle/123456789/16399-
dc.description.abstractVisible-light-induced, dehydrogenative spiro annulation of 2-arylquinazolin-4(3H)-ones with maleimides has been achieved at ambient conditions by merging Rh(III)-catalysis with photoredox catalysis. Various spirocyclized quinazolinone derivatives are synthesized with a broad substrate scope in up to 92% yields at room temperature. A further mechanistic study involving control experiments, UV spectroscopy, light on-off experiments, kinetic isotope effect study, H/D labeling study, and hydrogen peroxide detection tests has been explored. The present methodology is demonstrated to be effective for scale-up synthesis, enabling the efficient generation of the spirocyclic product. © 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.subjectCH activationen_US
dc.subjectdual catalysisen_US
dc.subjectheterocyclesen_US
dc.subjectspirocyclizationen_US
dc.subjectvisible lighten_US
dc.titleVisible-Light-Mediated Dual Catalytic Spiro Annulation of 2-Aryl Quinazolin-4(3H)-ones with N-Substituted Maleimidesen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

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