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Direct conversion of aldehydes into nitriles via O-phenylcarbamoylated aldoximes

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dc.contributor.buuauthorCoşkun, Necdet
dc.contributor.buuauthorArıkan, Nevin
dc.contributor.departmentFen Edebiyat Fakültesi
dc.contributor.departmentKimya Bölümü
dc.contributor.researcheridAAH-6337-2021tr_TR
dc.date.accessioned2021-07-06T06:17:37Z
dc.date.available2021-07-06T06:17:37Z
dc.date.issued1999-10-01
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.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.endpage11948tr_TR
dc.identifier.issn0040-4020
dc.identifier.issue40tr_TR
dc.identifier.scopus2-s2.0-0033213934tr_TR
dc.identifier.startpage11943tr_TR
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.identifier.volume55tr_TR
dc.identifier.wos000082710200018
dc.indexed.scopusScopusen_US
dc.indexed.wosSCIEen_US
dc.language.isoenen_US
dc.publisherPergamon-Elsevier Scienceen_US
dc.relation.journalTetrahedronen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectChemistryen_US
dc.subject.wosChemistry, organicen_US
dc.titleDirect conversion of aldehydes into nitriles via O-phenylcarbamoylated aldoximesen_US
dc.typeArticle
dc.wos.quartileQ2en_US
dspace.entity.typePublication
local.contributor.departmentFen Edebiyat Fakültesi/Kimya Bölümütr_TR

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