Regioselective synthesis of the 3,4-dihydrofuro[3,2-d]pyrimidin-2(1H)-one skeleton: a new class of compound

dc.authorid0000-0001-5001-2817
dc.authorid0000-0002-6311-8917
dc.contributor.authorKoza, Gani
dc.contributor.authorÖzcan, Sevil
dc.contributor.authorŞahin, Ertan
dc.contributor.authorBalcı, Metin
dc.date.accessioned2021-06-23T19:26:10Z
dc.date.available2021-06-23T19:26:10Z
dc.date.issued2009
dc.departmentBAİBÜ, Fen Edebiyat Fakültesi, Kimya Bölümüen_US
dc.description.abstractWe hereby report the first preparation of the 3,4-dihydrofuro[3,2-d]pyrimidin-2(1H)-one skeleton formed by two controlled Curtius rearrangements of the corresponding acyl azides, prepared from 2-(2-methoxy-2-oxoethyl)furan-3-carboxylate via the hydrazide. Rearrangement of the acyl azides followed by trapping by nucleophiles and intramolecular trapping provided the target compounds. (C) 2009 Elsevier Ltd. All rights reserved.en_US
dc.identifier.doi10.1016/j.tet.2009.05.090
dc.identifier.endpage5976en_US
dc.identifier.issn0040-4020
dc.identifier.issue31en_US
dc.identifier.startpage5973en_US
dc.identifier.urihttps://doi.org/10.1016/j.tet.2009.05.090
dc.identifier.urihttps://hdl.handle.net/20.500.12491/6444
dc.identifier.volume65en_US
dc.identifier.wosWOS:000268217000014en_US
dc.identifier.wosqualityQ1en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.institutionauthorÖzcan, Sevil
dc.language.isoenen_US
dc.publisherPergamon-Elsevier Science Ltden_US
dc.relation.ispartofTetrahedronen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectPyrimidinoneen_US
dc.subjectFuropyrimidinoneen_US
dc.subjectAcyl Azideen_US
dc.subjectAcyl Hydrazideen_US
dc.subjectCurtius Rearrangementen_US
dc.titleRegioselective synthesis of the 3,4-dihydrofuro[3,2-d]pyrimidin-2(1H)-one skeleton: a new class of compounden_US
dc.typeArticleen_US

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