Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12258/18180
Title: Electrophilically activated nitroalkanes in double annulation of [1,2,4]triazolo[4,3-a]quinolines and 1,3,4-oxadiazole rings
Authors: Aksenov, A. V.
Аксенов, А. В.
Kirilov, N. K.
Кирилов, Н. К.
Aksenov, N. A.
Аксенов, Н. А.
Aksenov, D. A.
Аксенов, Д. А.
Rubin, M. A.
Рубин, М. А.
Keywords: Annulation;Nitroalkanes;Cascade transformations;Heterocycles
Issue Date: 2021
Publisher: MDPI
Citation: Aksenov, 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/molecules26185692
Series/Report no.: Molecules
Abstract: Nitroalkanes 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.
URI: http://hdl.handle.net/20.500.12258/18180
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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