Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/18593
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dc.contributor.authorBishi, Sangitaen_US
dc.contributor.authorSarkar, Debayanen_US
dc.date.accessioned2026-07-09T06:48:12Z-
dc.date.available2026-07-09T06:48:12Z-
dc.date.issued2026-
dc.identifier.citationBishi, S., Pastore, G., Kreitmeier, P., Reiser, O., & Sarkar, D. (2026). Graphitic Carbon Nitride Enabled Photocatalytic Synthesis of 3-Hydroxyisoindolin-1-ones. European Journal of Organic Chemistry. https://doi.org/10.1002/ejoc.70597en_US
dc.identifier.issn1434-193X-
dc.identifier.otherEID(2-s2.0-105040764985)-
dc.identifier.urihttps://dx.doi.org/10.1002/ejoc.70597-
dc.identifier.urihttps://dspace.iiti.ac.in:8080/jspui/handle/123456789/18593-
dc.description.abstractWe report a sustainable and metal free approach for the benzylation of phthalimide derivatives using readily available (hetero)aryl acetic acids via a decarboxylative, visible-light-induced photooxidation process catalyzed by graphitic carbon nitride (g-C3N4) and afforded the desired benzylated products in excellent yields within a reaction time of 5–6 h. The methodology features a broad substrate scope and high functional group tolerance, accommodating diverse (hetero)aryl and phthalimide derivatives. Importantly, this protocol avoids the use of transition metals and harsh oxidants, operates under mild conditions, and benefits from the recyclability of the heterogeneous photocatalyst, making it an efficient and environmentally benign strategy for C-C bond formation. © 2026 Wiley-VCH GmbH.en_US
dc.language.isoenen_US
dc.publisherJohn Wiley and Sons Incen_US
dc.sourceEuropean Journal of Organic Chemistryen_US
dc.titleGraphitic Carbon Nitride Enabled Photocatalytic Synthesis of 3-Hydroxyisoindolin-1-onesen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

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