Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/123456789/29634
Title: An Oxidative SNH Alkylamination of 5(6,7,8)-Nitroquinoline N-Oxides in Aqueous Dioxane Medium
Authors: Larin, A. N.
Ларин, А. Н.
Avakyan, E. K.
Авакян, Е. К.
Demidov, O. P.
Демидов, О. П.
Borovleva, A. A.
Боровлева, А. А.
Pobedinskaya, D. Y.
Побединская, Д. Ю.
Ermolenko, A. P.
Ермоленко, А. П.
Kolosov, S. E.
Колосов, С. Е.
Borovlev, I. V.
Боровлев, И. В.
Keywords: Alkylamination;ONSH;C−H activation;Nitroquinoline N-oxides;Nucleophilic substitution of hydrogen
Issue Date: 2025
Publisher: John Wiley and Sons Inc
Citation: Larin, A.N., Avakyan, E.K., Demidov, O.P., Borovleva, A.A., Zubenko, A.A., Pobedinskaya, D.Y., Ermolenko, A.P., Kolosov, S.E., Borovlev, I.V. An Oxidative SNH Alkylamination of 5(6,7,8)-Nitroquinoline N-Oxides in Aqueous Dioxane Medium // European Journal of Organic Chemistry. - 2025. - 28 (3). - статья № e202401060. - DOI: 10.1002/ejoc.202401060
Series/Report no.: European Journal of Organic Chemistry
Abstract: A novel and efficient method for the synthesis of 2-alkylamino and 2-dialkylamino derivatives of N-oxides of 5-, 6-, 7- and 8-nitroquinolines, which can potentially exhibit biological activity, as containing a pharmacophoric quinoline fragment, is described herein. The reactions of 5(6,7,8)-nitroquinoline N-oxides with various primary or secondary amines in the presence of potassium ferricyanide at in aqueous dioxane medium afforded the corresponding secondary and tertiary amines in moderate to excellent yields. This reaction is the first example of a Chichibabin reaction leading to the formation of 2-alkylaminoquinoline derivatives at position 2 under mild conditions. A study of the antibacterial activity of some products was carried out.
URI: https://dspace.ncfu.ru/handle/123456789/29634
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

Files in This Item:
File Description SizeFormat 
scopusresults 3437.pdf
  Restricted Access
136.61 kBAdobe PDFView/Open
WoS 2072.pdf
  Restricted Access
126.49 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.