Tandem nitrosation/cycloaddition of heterocyclic enamines using nitrolic acids

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dc.authorid0000-0003-4740-1138en_US
dc.authorid0000-0002-0873-694Xen_US
dc.authorid0000-0002-8658-3897en_US
dc.contributor.authorAltuğ, Cevher
dc.contributor.authorDürüst, Yaşar
dc.contributor.authorElliott, Mark C.
dc.contributor.authorKariuki, Benson M.
dc.date.accessioned2021-06-23T19:26:08Z
dc.date.available2021-06-23T19:26:08Z
dc.date.issued2009
dc.departmentBAİBÜ, Fen Edebiyat Fakültesi, Kimya Bölümüen_US
dc.description.abstractThe reaction of alkylidenepyrrolidines with nitrolic acids gives rise to the formation of novel 3,7a-disubstituted (1,2,4-oxadiazol-5-yl)-5,6,7,7a-tetrahydropyrrolo[1,2-d][1,2,4]oxadiazoles. A plausible mechanism for this reaction is proposed, which features nitrosation of the enamine by the nitrous acid that is liberated from the nitrolic acid. (C) 2009 Elsevier Ltd. All rights reserved.en_US
dc.identifier.doi10.1016/j.tetlet.2009.06.065
dc.identifier.endpage4921en_US
dc.identifier.issn0040-4039
dc.identifier.issue34en_US
dc.identifier.scopus2-s2.0-67649854185en_US
dc.identifier.scopusqualityQ3en_US
dc.identifier.startpage4919en_US
dc.identifier.urihttps://doi.org/10.1016/j.tetlet.2009.06.065
dc.identifier.urihttps://hdl.handle.net/20.500.12491/6432
dc.identifier.volume50en_US
dc.identifier.wosWOS:000268508900032en_US
dc.identifier.wosqualityQ2en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.institutionauthorAltuğ, Cevher
dc.institutionauthorDürüst, Yaşar
dc.language.isoenen_US
dc.publisherPergamon-Elsevier Science Ltden_US
dc.relation.ispartofTetrahedron Lettersen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectTandemen_US
dc.titleTandem nitrosation/cycloaddition of heterocyclic enamines using nitrolic acidsen_US
dc.typeArticleen_US

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