1. Açık Erişim@BUU
  2. İndeksli Yayınlar
  3. Web of Science
Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/21095
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dc.date.accessioned2021-07-06T06:17:37Z-
dc.date.available2021-07-06T06:17:37Z-
dc.date.issued1999-10-01-
dc.identifier.citationCoşkun, N. ve Arıkan, N. (1999). "Direct conversion of aldehydes into nitriles via O-phenylcarbamoylated aldoximes". Tetrahedron, 55(40), 11943-11948.en_US
dc.identifier.issn0040-4020-
dc.identifier.urihttps://doi.org/10.1016/S0040-4020(99)00692-4-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0040402099006924-
dc.identifier.urihttp://hdl.handle.net/11452/21095-
dc.description.abstractO-Arylcarbamoylated hydroxylamine tosylate reacts with aldehydes at room temperature to give the corresponding O-carbamoylated oximes. The reaction of carbamoylated hydroxylamine with aromatic aldehydes in THF or in toluene at reflux affords the corresponding nitriles and anilinium tosylate in high yield. Attempts to cyclize compounds 2 in the presence of AcCl lead again to the formation of nitriles.en_US
dc.language.isoenen_US
dc.publisherPergamon-Elsevier Scienceen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectChemistryen_US
dc.titleDirect conversion of aldehydes into nitriles via O-phenylcarbamoylated aldoximesen_US
dc.typeArticleen_US
dc.identifier.wos000082710200018tr_TR
dc.identifier.scopus2-s2.0-0033213934tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Fen Edebiyat Fakültesi/Kimya Bölümü.tr_TR
dc.identifier.startpage11943tr_TR
dc.identifier.endpage11948tr_TR
dc.identifier.volume55tr_TR
dc.identifier.issue40tr_TR
dc.relation.journalTetrahedronen_US
dc.contributor.buuauthorCoşkun, Necdet-
dc.contributor.buuauthorArıkan, Nevin-
dc.contributor.researcheridAAH-6337-2021tr_TR
dc.subject.wosChemistry, organicen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.wos.quartileQ2en_US
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