Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/22177
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dc.date.accessioned2021-10-01T09:03:23Z-
dc.date.available2021-10-01T09:03:23Z-
dc.date.issued1999-
dc.identifier.citationCoşkun, N. vd. (1999). "Beckmann fragmentation of diphenylcarbamoylated N-aryldiphenacylamine dioximes. New method for the synthesis of imidazooxadiazolones". Synthetic Communications, 29(22), 3889-3894.en_US
dc.identifier.issn0039-7911-
dc.identifier.urihttps://doi.org/10.1080/00397919908085909-
dc.identifier.urihttps://www.tandfonline.com/doi/abs/10.1080/00397919908085909-
dc.identifier.urihttp://hdl.handle.net/11452/22177-
dc.description.abstractN-Aryl-N,N-diphenacylamine dioximes were prepared by the reaction of corresponding arylamines with alpha-bromoacetophenone oxime in ethanol-water at room temperature. These compounds reacted with aryl isocyanates in acetonitrile to give imidazooxadiazolones 9. The probable mechanism of the reaction is discussed.en_US
dc.language.isoenen_US
dc.publisherTaylor & Francisen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectChemistryen_US
dc.subjectCarbon bond formationen_US
dc.subjectDiastereoselective additionen_US
dc.subjectOrganoaluminum reagentsen_US
dc.subjectImidazoline 3-oxidesen_US
dc.subjectAryl isocyanatesen_US
dc.subjectOximeen_US
dc.subjectRegioen_US
dc.titleBeckmann fragmentation of diphenylcarbamoylated N-aryldiphenacylamine dioximes. New method for the synthesis of imidazooxadiazolonesen_US
dc.typeArticleen_US
dc.identifier.wos000082688900005tr_TR
dc.identifier.scopus2-s2.0-0344562884tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Fen Edebiyat Fakültesi/Kimya Bölümü.tr_TR
dc.identifier.startpage3889tr_TR
dc.identifier.endpage3894tr_TR
dc.identifier.volume29tr_TR
dc.identifier.issue22tr_TR
dc.relation.journalSynthetic Communicationsen_US
dc.contributor.buuauthorCoşkun, Necdet-
dc.contributor.buuauthorTat, Fatma Tirli-
dc.contributor.buuauthorGüven, Özden Özel-
dc.subject.wosChemistry, organicen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.wos.quartileQ3en_US
dc.subject.scopusKendomycin; Allylation; Acetal Derivativeen_US
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