Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/14941
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dc.contributor.authorLadumor, Ravikumaren_US
dc.contributor.authorSamanta, Souraven_US
dc.contributor.authorSermadurai, Selvakumaren_US
dc.date.accessioned2024-12-18T10:34:09Z-
dc.date.available2024-12-18T10:34:09Z-
dc.date.issued2024-
dc.identifier.citationLadumor, R., Samanta, S., & Selvakumar, S. (2024). Photocatalytic Silylation of Aryl Alkynoates: Synthesis of Silylated Coumarins. Advanced Synthesis and Catalysis. Scopus. https://doi.org/10.1002/adsc.202401007en_US
dc.identifier.issn1615-4150-
dc.identifier.otherEID(2-s2.0-85206907460)-
dc.identifier.urihttps://doi.org/10.1002/adsc.202401007-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/14941-
dc.description.abstractHerein, we report the photocatalytic synthesis of 3-silyl coumarins using hydrosilanes as the silyl radical source with aryl alkynoates. Readily prepared N-aminopyridinium salts act as hydrogen atom transfer reagents for generating silyl radicals under photoredox catalysis. The reaction proceeds through a silyl radical addition to alkyne followed by radical cascade cyclization/migration with subsequent oxidation and aromatization to give the desired 3-silyl coumarins in 34–89% yield. © 2024 Wiley-VCH GmbH.en_US
dc.language.isoenen_US
dc.publisherJohn Wiley and Sons Incen_US
dc.sourceAdvanced Synthesis and Catalysisen_US
dc.subjectCoumarinen_US
dc.subjectHydrogen atom transferen_US
dc.subjectPhotocatalysisen_US
dc.subjectRadicalsen_US
dc.subjectSilylationen_US
dc.titlePhotocatalytic Silylation of Aryl Alkynoates: Synthesis of Silylated Coumarinsen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

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