Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12258/18827
Title: Electrophilically activated nitroalkanes in the synthesis of substituted 1,3,4-oxadiazoles from amino acid derivatives
Authors: Aksenov, A. V.
Аксенов, А. В.
Kirilov, N. K.
Кирилов, Н. К.
Aksenov, N. A.
Аксенов, Н. А.
Arutiunov, N. A.
Арутюнов, Н. А.
Aksenov, D. A.
Аксенов, Д. А.
Rubin, M. A.
Рубин, М. А.
Keywords: 1,3,4-oxadiazoles;1,3,4-thiadiazoles;Amino acids;Brønsted acid catalysis;Cascade reaction;Nitroalkanes;Nucleophilic cycloaddition;Semicarbazides
Issue Date: 2022
Publisher: Springer
Citation: Aksenov, 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/s10593-022-03053-2
Series/Report no.: Chemistry of Heterocyclic Compounds
Abstract: Novel 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.
URI: http://hdl.handle.net/20.500.12258/18827
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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