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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.authorArutiunov, N. A.-
dc.contributor.authorАрутюнов, Н. А.-
dc.contributor.authorAksenov, D. A.-
dc.contributor.authorАксенов, Д. А.-
dc.contributor.authorRubin, M. A.-
dc.contributor.authorРубин, М. А.-
dc.date.accessioned2022-02-14T08:53:05Z-
dc.date.available2022-02-14T08:53:05Z-
dc.date.issued2022-
dc.identifier.citationAksenov, A. V., Kirilov, N. K., Aksenov, N. A., Arutiunov, N. A., Aksenov, D. A., Rubin, M. A. Electrophilically activated nitroalkanes in the synthesis of substituted 1,3,4-oxadiazoles from amino acid derivatives // Chemistry of Heterocyclic Compounds. - 2022. - DOI10.1007/s10593-022-03053-2ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/18827-
dc.description.abstractNovel preparative approach for the synthesis of alkylamines with 1,3,4-oxadiazole heterocyclic substituent is described. This method is based on unusual cascade transformation involving formal (4+1) cyclocondensation of hydrazides of amino acids with nitroalkanes electrophilically activated in the presence of polyphosphoric acid.ru
dc.language.isoenru
dc.publisherSpringerru
dc.relation.ispartofseriesChemistry of Heterocyclic Compounds-
dc.subject1,3,4-oxadiazolesru
dc.subject1,3,4-thiadiazolesru
dc.subjectAmino acidsru
dc.subjectBrønsted acid catalysisru
dc.subjectCascade reactionru
dc.subjectNitroalkanesru
dc.subjectNucleophilic cycloadditionru
dc.subjectSemicarbazidesru
dc.titleElectrophilically activated nitroalkanes in the synthesis of substituted 1,3,4-oxadiazoles from amino acid derivativesru
dc.typeСтатьяru
vkr.instХимико-фармацевтический факультетru
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