Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/65753
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dc.contributor.authorShit, Ranjit Kumar-
dc.contributor.authorSinha, Nitai Chand-
dc.date.accessioned2025-04-25T05:34:25Z-
dc.date.available2025-04-25T05:34:25Z-
dc.date.issued2025-04-
dc.identifier.issnISSN: 2583-1321 (Online);ISSN: 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/65753-
dc.description441-446en_US
dc.description.abstractThe higher degree of chemoselctivitiy and regioselectivity recorded during the selenium dioxide oxidation of various coumarinyl ketones 1-7 affords the corresponding coumarinyl α-di carbonyl compounds 1a-7a and 5b in which the compound 2a has been isolated as an unexpected product and also the sodium borohydride reduction of coumarinyl ketones 1-14 affords the desired coumarinyl carbinols 1c-3c, 5c, 7c-9c, 11c and 13c and 5-keto-6-hydroxy-cinnamic acid derivatives 4d, 6d, 10d, 12d and 14d as unexpected products in minor amounts.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR, Indiaen_US
dc.sourceIJC Vol.64(04) [April 2025]en_US
dc.subjectAssorteden_US
dc.subjectChemoselectivityen_US
dc.subjectDerivativesen_US
dc.subjectEpoxidesen_US
dc.subjectOxidationen_US
dc.subjectReductionen_US
dc.subjectUnusualen_US
dc.titleApplications of oxidative and reductive methodologies on coumarinyl ketonesen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.56042/ijc.v64i4.15225en_US
Appears in Collections:IJC Vol.64(04) [April 2025]

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