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dc.contributor.authorSteparuk, E. V.en
dc.contributor.authorObydennov, D. L.en
dc.contributor.authorSosnovskikh, V. Y.en
dc.date.accessioned2024-04-05T16:26:53Z-
dc.date.available2024-04-05T16:26:53Z-
dc.date.issued2023-
dc.identifier.citationSteparuk, EV, Obydennov, DL & Sosnovskikh, VY 2023, 'Synthesis of 5-Aroyl-2-aryl-3-hydroxypyridin-4(1H)-ones', Molbank, Том. 2023, № 2, M1668. https://doi.org/10.3390/M1668harvard_pure
dc.identifier.citationSteparuk, E. V., Obydennov, D. L., & Sosnovskikh, V. Y. (2023). Synthesis of 5-Aroyl-2-aryl-3-hydroxypyridin-4(1H)-ones. Molbank, 2023(2), [M1668]. https://doi.org/10.3390/M1668apa_pure
dc.identifier.issn1422-8599-
dc.identifier.otherFinal2
dc.identifier.otherAll Open Access, Gold3
dc.identifier.otherhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85163774687&doi=10.3390%2fM1668&partnerID=40&md5=d9b3c036381ac8e9adb20f55bb6e5c391
dc.identifier.otherhttps://www.mdpi.com/1422-8599/2023/2/M1668/pdf?version=1687153588pdf
dc.identifier.urihttp://elar.urfu.ru/handle/10995/130596-
dc.description.abstractA two-stage synthesis of 5-aroyl-2-aryl-3-hydroxypyridin-4(1H)-ones (56–66% overall yields) was carried out by refluxing 5-aroyl-3-(benzyloxy)-2-(het)aryl-4H-pyran-4-ones with ammonium acetate in AcOH and subsequent debenzylation. The prepared N-unsubstituted 4-pyridones exist in the pyridone tautomeric form. © 2023 by the authors.en
dc.description.sponsorshipRussian Science Foundation, RSF: 22-73-10236en
dc.description.sponsorshipThis research was funded by the Russian Science Foundation, grant number 22-73-10236 (https://rscf.ru/project/22-73-10236/ (accessed on 24 April 2023)).en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherMDPIen
dc.relationinfo:eu-repo/grantAgreement/RSF//22-73-10236en
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.rightscc-byother
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/unpaywall
dc.sourceMolbank2
dc.sourceMolBanken
dc.subject3-HYDROXY-4-PYRIDONESen
dc.subject4-PYRONESen
dc.subjectCHELATING AGENTSen
dc.subjectDEBENZYLATIONen
dc.subjectMETALLOENZYME INHIBITORSen
dc.subjectTAUTOMERISMen
dc.titleSynthesis of 5-Aroyl-2-aryl-3-hydroxypyridin-4(1H)-onesen
dc.typeArticleen
dc.typeinfo:eu-repo/semantics/articleen
dc.type|info:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.3390/M1668-
dc.identifier.scopus85163774687-
local.contributor.employeeSteparuk, E.V., Institute of Natural Sciences and Mathematics, Ural Federal University, 51 Lenina ave, Ekaterinburg, 620000, Russian Federationen
local.contributor.employeeObydennov, D.L., Institute of Natural Sciences and Mathematics, Ural Federal University, 51 Lenina ave, Ekaterinburg, 620000, Russian Federationen
local.contributor.employeeSosnovskikh, V.Y., Institute of Natural Sciences and Mathematics, Ural Federal University, 51 Lenina ave, Ekaterinburg, 620000, Russian Federationen
local.issue2-
local.volume2023-
dc.identifier.wos001017254100001-
local.contributor.departmentInstitute of Natural Sciences and Mathematics, Ural Federal University, 51 Lenina ave, Ekaterinburg, 620000, Russian Federationen
local.identifier.pure41528523-
local.description.orderM1668-
local.identifier.eid2-s2.0-85163774687-
local.fund.rsf22-73-10236-
local.identifier.wosWOS:001017254100001-
Располагается в коллекциях:Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC

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