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dc.contributor.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.contributor.authorAksenov, D. A.-
dc.contributor.authorАксенов, Д. А.-
dc.contributor.authorGanusenko, D. D.-
dc.contributor.authorГанусенко, Д. Д.-
dc.contributor.authorKurenkov, I. A.-
dc.contributor.authorКуренков, И. А.-
dc.contributor.authorLeontiev, A. V.-
dc.contributor.authorЛеонтьев, А. В.-
dc.contributor.authorAksenov, A. V.-
dc.contributor.authorАксенов, А. В.-
dc.date.accessioned2023-06-29T08:13:36Z-
dc.date.available2023-06-29T08:13:36Z-
dc.date.issued2023-
dc.identifier.citationAksenov N.A., Aksenov D.A., Ganusenko D.D., Kurenkov I.A., Leontiev A.V., Aksenov A.V. Synthesis of 2-carboxyaniline-substituted maleimides from 2'-nitrochalcones // Organic & biomolecular chemistry. - 2023. - 21(15), pp. 3156-3166. - DOI: 10.1039/d3ob00197kru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/23767-
dc.description.abstractA practical, one-pot approach to 3-anilino-4-(het)arylmaleimides by simple heating of aqueous DMSO solution of 2′-nitrochalcones with potassium cyanide in the presence of formic acid has been developed. This new reaction provides effective access to a variety of β-substituted α-aminomaleimides which have recently become a subject of growing interest as small, easily modified and environmentally responsive fluorescent probes.ru
dc.language.isoenru
dc.relation.ispartofseriesOrganic and Biomolecular Chemistry-
dc.subjectFluorescent probesru
dc.subject3-anilino-4-(het)arylmaleimidesru
dc.subjectβ-substituted α-aminomaleimidesru
dc.titleSynthesis of 2-carboxyaniline-substituted maleimides from 2'-nitrochalconesru
dc.typeСтатьяru
vkr.instХимико-фармацевтический факультетru
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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