Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/19711
Title: SNH Amidation of 5(6,7,8)-nitroquinoline N-oxides
Authors: Borovleva, A. A.
Боровлева, А. А.
Avakyan, E. K.
Авакян, Е. К.
Amangasieva, G. A.
Амангазиева, Г. А.
Demidov, O. P.
Демидов, О. П.
Pobedinskaya, D. Y.
Побединская, Д. Ю.
Ermolenko, A. P.
Ермоленко, А. П.
Larin, A. N.
Ларин, А. Н.
Borovlev, I. V.
Боровлев, И. В.
Keywords: 5(6,7,8)-nitroquinoline N-oxides;Disproportionation;N-(nitro(nitroso)-1-oxidoquinolinyl)benzamides;SNH amidation
Issue Date: 2022
Publisher: Springer
Citation: Borovleva, A. A., Avakyan, E. K., Amangasieva, G. A., Demidov, O. P., Pobedinskaya, D. Y., Ermolenko, A. P., Larin, A. N., Borovlev, I. V. SNH Amidation of 5(6,7,8)-nitroquinoline N-oxides // Chemistry of Heterocyclic Compounds. - 2022. - DOI10.1007/s10593-022-03077-8
Series/Report no.: Chemistry of Heterocyclic Compounds
Abstract: Direct SNH amidation of 6- and 7-nitroquinoline N-oxides in anhydrous DMSO allowed to obtain N-oxides of 2- and 8-aroylaminonitroquinolines, respectively. 5-Nitroquinoline N-oxide was transformed into a mixture of amides derived from the N-oxides of 5-nitroand 5-nitrosoquinolines. 8-Nitroquinoline N-oxide underwent destruction under the same conditions.
URI: http://hdl.handle.net/20.500.12258/19711
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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