Publication:
Direct conversion of aldehydes into nitriles via O-phenylcarbamoylated aldoximes

dc.contributor.buuauthorCoşkun, Necdet
dc.contributor.buuauthorArıkan, Nevin
dc.contributor.departmentFen Edebiyat Fakültesi
dc.contributor.departmentKimya Bölümü
dc.contributor.researcheridAAH-6337-2021
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.
dc.identifier.citationCoşkun, N. ve Arıkan, N. (1999). "Direct conversion of aldehydes into nitriles via O-phenylcarbamoylated aldoximes". Tetrahedron, 55(40), 11943-11948.
dc.identifier.endpage11948
dc.identifier.issn0040-4020
dc.identifier.issue40
dc.identifier.scopus2-s2.0-0033213934
dc.identifier.startpage11943
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.volume55
dc.identifier.wos000082710200018
dc.indexed.scopusScopus
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherPergamon-Elsevier Science
dc.relation.journalTetrahedron
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectChemistry
dc.subject.wosChemistry, organic
dc.titleDirect conversion of aldehydes into nitriles via O-phenylcarbamoylated aldoximes
dc.typeArticle
dc.wos.quartileQ2
dspace.entity.typePublication
local.contributor.departmentFen Edebiyat Fakültesi/Kimya Bölümü
local.indexed.atWOS
local.indexed.atScopus

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