Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/18180
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dc.contributor.authorAksenov, A. V.-
dc.contributor.authorАксенов, А. В.-
dc.contributor.authorKirilov, N. K.-
dc.contributor.authorКирилов, Н. К.-
dc.contributor.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.contributor.authorAksenov, D. A.-
dc.contributor.authorАксенов, Д. А.-
dc.contributor.authorRubin, M. A.-
dc.contributor.authorРубин, М. А.-
dc.date.accessioned2021-10-11T09:34:44Z-
dc.date.available2021-10-11T09:34:44Z-
dc.date.issued2021-
dc.identifier.citationAksenov, A. V.; Kirilov, N. K.; Aksenov, N. A.; Aksenov, D. A.; Sorokina E. A.; Lower, C.; Rubin, M. A. Electrophilically activated nitroalkanes in double annulation of [1,2,4]triazolo[4,3-a]quinolines and 1,3,4-oxadiazole rings // Molecules. - 2021. - Том 26. - Выпуск 18. - Номер статьи 5692. - DOI 10.3390/molecules26185692ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/18180-
dc.description.abstractNitroalkanes activated with polyphosphoric acid could serve as efficient electrophiles in reactions with amines and hydrazines, enabling various cascade transformations toward heterocyclic systems. This strategy was developed for an innovative synthetic protocol employing simultaneous or sequential annulation of two different heterocyclic cores, affording [1,2,4]triazolo[4,3-a]quinolines with 1,3,4-oxadiazole substituents.ru
dc.language.isoenru
dc.publisherMDPIru
dc.relation.ispartofseriesMolecules-
dc.subjectAnnulationru
dc.subjectNitroalkanesru
dc.subjectCascade transformationsru
dc.subjectHeterocyclesru
dc.titleElectrophilically activated nitroalkanes in double annulation of [1,2,4]triazolo[4,3-a]quinolines and 1,3,4-oxadiazole ringsru
dc.typeСтатьяru
vkr.instХимико-фармацевтический факультетru
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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