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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/26447
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dc.contributor.authorAksenov, A. V.-
dc.contributor.authorАксенов, А. В.-
dc.contributor.authorArutiunov, N. A.-
dc.contributor.authorАрутюнов, Н. А.-
dc.contributor.authorZatsepilina, A. M.-
dc.contributor.authorЗацепилина, А. М.-
dc.contributor.authorAksenova, A. A.-
dc.contributor.authorАксенова, А. А.-
dc.contributor.authorAleksandrova, E. V.-
dc.contributor.authorАлександрова, Е. В.-
dc.contributor.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.contributor.authorLeontiev, A. V.-
dc.contributor.authorЛеонтьев, А. В.-
dc.contributor.authorAksenov, D. A.-
dc.contributor.authorАксенов, Д. А.-
dc.date.accessioned2024-02-12T13:01:15Z-
dc.date.available2024-02-12T13:01:15Z-
dc.date.issued2024-
dc.identifier.citationAksenov, A.V., Arutiunov, N.A., Zatsepilina, A.M., Aksenova, A.A., Aleksandrova, E.V., Aksenov, N.A., Leontiev, A.V., Aksenov, D.A. Novel Two-Step Synthesis of N -Alkylated 2,3-Diaryl-4-quinolones // Synthesis (Germany). - 2024. - 56 (3). - pp. 435-444. - DOI: 10.1055/s-0042-1751530ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/26447-
dc.description.abstractA library of 18 polysubstituted 4-quinolones was conveniently prepared via simple and practical protocol involving N-alkylation of 2-(3-oxoindolin-2-yl)acetonitriles and following NaH-induced ring expansion. The current two-step approach provides feasible access to a subclass of N-protected C3-aryl-substituted 2-phenyl-4-quinolones starting with or just one step away from commercially available 2- arylindoles and nitrostyrenes.ru
dc.language.isoenru
dc.relation.ispartofseriesSynthesis (Germany)-
dc.subject4-quinolonesru
dc.subjectNitroalkenesru
dc.subjectCascade transformationsru
dc.subjectIndolesru
dc.subjectRearrangementru
dc.subjectSodium compoundsru
dc.titleNovel Two-Step Synthesis of N -Alkylated 2,3-Diaryl-4-quinolonesru
dc.typeСтатьяru
vkr.instХимико-фармацевтический факультетru
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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