Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/15945
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dc.contributor.authorKshirsagar, Umesh Achyutraoen_US
dc.date.accessioned2025-04-22T17:45:34Z-
dc.date.available2025-04-22T17:45:34Z-
dc.date.issued2025-
dc.identifier.citationNandini, R., Hegde, R. v, Grzegorz Małecki, J., Kshirsagar, U. A., Patil, S. A., Mane, M. v, & Dateer, R. B. (2025). Metal and Base-Free Synthesis of Benzoxazino and Benzoxazepino Fused Isoquinolines: A DFT Insight and Photophysical Study. Advanced Synthesis and Catalysis. https://doi.org/10.1002/adsc.202500014en_US
dc.identifier.issn1615-4150-
dc.identifier.otherEID(2-s2.0-105002247097)-
dc.identifier.urihttps://doi.org/10.1002/adsc.202500014-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/15945-
dc.description.abstractA novel metal- and base-free approach for the synthesis of benzoxazino and benzoxazepino fused isoquinoline derivatives from ortho-alkynyl aldehydes and amines under mild reaction conditions has been described. The formation of new C−O and C−N bonds via metal-free cyclization with internal alkyne aided by water molecules without using external ligands and bases has been described. In addition, a series of control experiments are performed, and mechanistic studies are discussed elaborately by Density Functional Theory (DFT) calculation. Furthermore, gram-scale synthesis and photophysical studies of the synthesized compounds and their quantum yield calculation have been demonstrated. © 2025 Wiley-VCH GmbH.en_US
dc.language.isoenen_US
dc.publisherJohn Wiley and Sons Incen_US
dc.sourceAdvanced Synthesis and Catalysisen_US
dc.subjectBenzoxazepino fused isoquinolinesen_US
dc.subjectBenzoxazino fused isoquinolinesen_US
dc.subjectDFT studyen_US
dc.subjectmetal-free approachen_US
dc.subjectphotophysical studyen_US
dc.titleMetal and Base-Free Synthesis of Benzoxazino and Benzoxazepino Fused Isoquinolines: A DFT Insight and Photophysical Studyen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

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