Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/12594
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dc.contributor.authorChillal, Abhinay S.en_US
dc.contributor.authorBhawale, Rajesh T.en_US
dc.contributor.authorKshirsagar, Umesh Achyutraoen_US
dc.date.accessioned2023-12-14T12:37:47Z-
dc.date.available2023-12-14T12:37:47Z-
dc.date.issued2023-
dc.identifier.citationChillal, A. S., Bhawale, R. T., & Kshirsagar, U. A. (2023). Photoinduced Regioselective Chalcogenation and Thiocyanation of 4H-Pyrido[1,2-a] pyrimidin-4-ones Under Benign Conditions. European Journal of Organic Chemistry. Scopus. https://doi.org/10.1002/ejoc.202300665en_US
dc.identifier.issn1434-193X-
dc.identifier.otherEID(2-s2.0-85166306094)-
dc.identifier.urihttps://doi.org/10.1002/ejoc.202300665-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/12594-
dc.description.abstractA lenient approach for regioselective C3−H chalcogenation and thiocyanation of 4H-pyrido[1,2-a] pyrimidin-4-ones is developed using visible light photocatalysis. This operationally straightforward method furnishes a broad array of C-3, Ar−S/Ar−Se and -SCN functionalized derivatives in moderate to high yields. This protocol employs visible light as an environmentally friendly energy source, cost effective inorganic persulfate-based oxidant and easily procurable dichalcogenides for regioselective C−H chalcogenation of the substrate at room temperature. Further, regioselective thiocyanation of 4H-pyrido[1,2-a] pyrimidin-4-ones was also developed. Mechanistic path for these transformations has been proposed based on light on/off and Stern-Volmer studies as well as quantum yield calculations. © 2023 Wiley-VCH GmbH.en_US
dc.language.isoenen_US
dc.publisherJohn Wiley and Sons Incen_US
dc.sourceEuropean Journal of Organic Chemistryen_US
dc.subjectC−H Functionalizationen_US
dc.subjectPhotocatalysisen_US
dc.subjectPyrido[1,2-a] pyrimidin-4-onesen_US
dc.subjectRegioselectiveen_US
dc.subjectVisible lighten_US
dc.titlePhotoinduced Regioselective Chalcogenation and Thiocyanation of 4H-Pyrido[1,2-a] pyrimidin-4-ones Under Benign Conditionsen_US
dc.typeJournal Articleen_US
dc.rights.licenseAll Open Access, Bronze-
Appears in Collections:Department of Chemistry

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