1. Açık Erişim@BUU
  2. İndeksli Yayınlar
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Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/34661
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dc.contributor.authorAsutay, Oktay-
dc.contributor.authorHamarat, Nilüfer-
dc.contributor.authorUludağ, Nesimi-
dc.date.accessioned2023-10-30T08:15:44Z-
dc.date.available2023-10-30T08:15:44Z-
dc.date.issued2015-06-17-
dc.identifier.citationAsutay, O. vd. (2015). "Selective oxidative deoximation with anhydrous Ce(IV) sulfate". Tetrahedron Letters, 56(25), 3902-3904.en_US
dc.identifier.issn0040-4039-
dc.identifier.urihttps://doi.org/10.1016/j.tetlet.2015.04.111-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0040403915007686-
dc.identifier.urihttp://hdl.handle.net/11452/34661-
dc.description.abstractAnhydrous Ce(SO4)(2) in chloroform selectively converts oximes into the parent carbonyl compounds in good yields. Hammett correlations helped to indicate a plausible mechanism for the above reaction. The formation of 1-(dinitromethyl)benzene was assumed to be a product of isonitroso hydrogen reaction with arylaldoximes.en_US
dc.description.sponsorshipNamık Kemal Üniversitesi (NKUBAP.00.M6.AR.12.01)en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectChemistryen_US
dc.subjectOxidationen_US
dc.subjectOximesen_US
dc.subjectReaction mechanismen_US
dc.subjectHammett correlationen_US
dc.subjectIsonitroso hydrogenen_US
dc.subjectParent carbonyl-compoundsen_US
dc.subjectOne-pot synthesisen_US
dc.subjectPreparative conversionen_US
dc.subjectEfficienten_US
dc.subjectRegenerationen_US
dc.subjectDerivativesen_US
dc.subjectNitrateen_US
dc.titleSelective oxidative deoximation with anhydrous Ce(IV) sulfateen_US
dc.typeArticleen_US
dc.identifier.wos000356549600013tr_TR
dc.identifier.scopus2-s2.0-84930181671tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü.tr_TR
dc.relation.bapNKUBAP.00.M6.AR.12.01tr_TR
dc.identifier.startpage3902tr_TR
dc.identifier.endpage3904tr_TR
dc.identifier.volume56tr_TR
dc.identifier.issue25tr_TR
dc.relation.journalTetrahedron Lettersen_US
dc.contributor.buuauthorCoşkun, Necdet-
dc.contributor.researcheridB-1200-2012tr_TR
dc.relation.collaborationYurt içitr_TR
dc.subject.wosChemistry, organicen_US
dc.indexed.wosSCIEen_US
dc.indexed.wosCCREen_US
dc.indexed.scopusScopusen_US
dc.wos.quartileQ2en_US
dc.contributor.scopusid7004177880tr_TR
dc.subject.scopusOximes; Carbonyl derivative; Ketoneen_US
dc.subject.emtree1 (dinitromethyl)benzeneen_US
dc.subject.emtreeBenzeneen_US
dc.subject.emtreeCarbonyl derivativeen_US
dc.subject.emtreeCeriumen_US
dc.subject.emtreeChlorinated hydrocarbonen_US
dc.subject.emtreeChloroformen_US
dc.subject.emtreeHydrogenen_US
dc.subject.emtreeNitrile oxideen_US
dc.subject.emtreeOximeen_US
dc.subject.emtreeSulfateen_US
dc.subject.emtreeUnclassified drugen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeChemical reactionen_US
dc.subject.emtreeOxidative deoximationen_US
dc.subject.emtreeRoom temperatureen_US
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