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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/123456789/32013
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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.authorMalyuga, V. V.-
dc.contributor.authorМалюга, В. В.-
dc.contributor.authorAksenov, D. A.-
dc.contributor.authorАксенов, Д. А.-
dc.contributor.authorDzhioeva, R. G.-
dc.contributor.authorДжиоева, Р. Г.-
dc.contributor.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.date.accessioned2025-09-08T09:43:41Z-
dc.date.available2025-09-08T09:43:41Z-
dc.date.issued2025-
dc.identifier.citationAksenov, A. V., Grishin, I. Y, Malyuga, V. V., Aksenov, D. A., Dzhioeva, R. G., Aksenov, N. A. α-Alkyl-α-nitro ketones as 1,2- and 1,1-biselectrophiles. Synthesis of benzoxazoles, benzimidazoles, and quinoxalines // Russian Chemical Bulletin. - 2025. - 74 (7). - pp. 2114 - 2124. - DOI: 10.1007/s11172-025-4695-2ru
dc.identifier.urihttps://dspace.ncfu.ru/handle/123456789/32013-
dc.description.abstractThe reactivity of α-alkyl-α-nitroacetophenones with 1,2-phenylenediamines and o-aminophenols in acidic medium was examined. The reaction pathway depends on the catalyst used and provides access to the corresponding benzoxazoles, benzimidazoles, and quinoxalines via the aza-Nef-type reaction.ru
dc.language.isoenru
dc.publisherSpringerru
dc.relation.ispartofseriesRussian Chemical Bulletin-
dc.subjectBiselectrophilesru
dc.subjectPolyphosphoric acidru
dc.subjectBisnucleophilesru
dc.subjectHeterocyclizationru
dc.subjectNitro ketonesru
dc.titleα-Alkyl-α-nitro ketones as 1,2- and 1,1-biselectrophiles. Synthesis of benzoxazoles, benzimidazoles, and quinoxalinesru
dc.typeСтатьяru
vkr.instХимический факультетru
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