Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/18044
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dc.contributor.authorAksenov, A. V.-
dc.contributor.authorАксенов, А. В.-
dc.contributor.authorGrishin, I. Y.-
dc.contributor.authorГришин, И. Ю.-
dc.contributor.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.contributor.authorMalyuga, V. V.-
dc.contributor.authorМалюга, В. В.-
dc.contributor.authorAksenov, D. A.-
dc.contributor.authorАксенов, Д. А.-
dc.contributor.authorRubin, M. A.-
dc.contributor.authorРубин, М. А.-
dc.date.accessioned2021-08-30T14:26:00Z-
dc.date.available2021-08-30T14:26:00Z-
dc.date.issued2021-
dc.identifier.citationAksenov, A.V., Grishin, I. Y., Aksenov, N. A., Malyuga, V. V., Aksenov, D. A., Nobi, M. A., Rubin, M. A. Electrophilically activated nitroalkanes in synthesis of 3,4-dihydroquinozalines // Molecules. - 2021. - Том 26. - Выпуск 142. - Номер статьи 4274ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/18044-
dc.description.abstractNitroalkanes activated with polyphosphoric acid serve as efficient electrophiles in reactions with various nucleophilic amines. Strategically placed second functionality allows for the design of annulation reactions enabling preparation of various heterocycles. This strategy was employed to develop an innovative synthetic approach towards 3,4-dihydroquinazolines from readily available 2-(aminomethyl)anilinesru
dc.language.isoenru
dc.publisherMDPI AGru
dc.relation.ispartofseriesMolecules-
dc.subjectAnnulationru
dc.subjectQuinozalinesru
dc.subjectHeterocyclic compoundsru
dc.subjectNitroalkanesru
dc.titleElectrophilically activated nitroalkanes in synthesis of 3,4-dihydroquinozalinesru
dc.typeСтатьяru
vkr.instХимико-фармацевтический факультетru
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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