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dc.contributor.authorSrinivas, V.-
dc.contributor.authorRao, V.R.-
dc.date.accessioned2025-05-20T05:12:43Z-
dc.date.available2025-05-20T05:12:43Z-
dc.date.issued2011-11-
dc.identifier.citation10.1002/jhet.849en_US
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/3276-
dc.descriptionNITWen_US
dc.description.abstractAn efficient zinc chloride-catalyzed one-pot synthesis of 5,8-dihydro-5,8-dioxo-4H-chromene derivatives have been achieved by the reaction of 2,5-dihydroxy-6-undecyl-1,4-bezoquinone, cyanothioacetamide, and aromaticaldehyde, in EtOH at room temperature. The structures of the products were characterized by IR, 1H-NMR, mass spectra, and elemental analyses. J.en_US
dc.language.isoenen_US
dc.publisherJournal of Heterocyclic Chemistryen_US
dc.subjectZinc chloride5,8-dihydro-5,8-dioxo-4H-chromeneen_US
dc.subject5,8-dihydro-5,8-dioxo-4H-chromeneen_US
dc.titleZinc chloride-catalyzed one-pot, three-component synthesis of 5,8-dihydro-5,8-dioxo-4H-chromene derivativesen_US
dc.typeArticleen_US
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