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DC Field | Value | Language |
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dc.contributor.author | Kirwale, Amol Bhivrao | en_US |
dc.contributor.author | Bhawale, Rajesh T. | en_US |
dc.contributor.author | Kshirsagar, Umesh Achyutrao | en_US |
dc.date.accessioned | 2025-07-09T13:48:00Z | - |
dc.date.available | 2025-07-09T13:48:00Z | - |
dc.date.issued | 2025 | - |
dc.identifier.citation | Kirwale, 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.202500462 | en_US |
dc.identifier.issn | 1434-193X | - |
dc.identifier.other | EID(2-s2.0-105008537564) | - |
dc.identifier.uri | https://dx.doi.org/10.1002/ejoc.202500462 | - |
dc.identifier.uri | https://dspace.iiti.ac.in:8080/jspui/handle/123456789/16399 | - |
dc.description.abstract | Visible-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.iso | en | en_US |
dc.publisher | John Wiley and Sons Inc | en_US |
dc.source | European Journal of Organic Chemistry | en_US |
dc.subject | CH activation | en_US |
dc.subject | dual catalysis | en_US |
dc.subject | heterocycles | en_US |
dc.subject | spirocyclization | en_US |
dc.subject | visible light | en_US |
dc.title | Visible-Light-Mediated Dual Catalytic Spiro Annulation of 2-Aryl Quinazolin-4(3H)-ones with N-Substituted Maleimides | en_US |
dc.type | Journal Article | en_US |
Appears in Collections: | Department of Chemistry |
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