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Title: Synthesis of amides by nucleophilic substitution of hydrogen in 3-nitropyridine
Authors: Amangasieva, G. A.
Амангазиева, Г. А.
Borovlev, I. V.
Боровлев, И. В.
Demidov, O. P.
Демидов, О. П.
Avakyan, E. K.
Авакян, Е. К.
Borovleva, A. A.
Боровлева, А. А.
Keywords: Synthesis of amides;Nucleophilic substitution
Issue Date: 2018
Publisher: Pleiades Publishing
Citation: Amangasieva, G.A., Borovlev, I.V., Demidov, O.P., Avakyan, E.K., Borovleva, A.A. Synthesis of amides by nucleophilic substitution of hydrogen in 3-nitropyridine // Russian Journal of Organic Chemistry. - 2018. - Volume 54. - Issue 6. - Pages 867-872
Series/Report no.: Russian Journal of Organic Chemistry
Abstract: 3-Nitropyridine reacted with nitrogen-centered carboxylic acid amide anions in anhydrous DMSO in the presence of K3Fe(CN)6 via oxidative nucleophilic substitution of hydrogen to give previously unknown N-(5-nitropyridin-2-yl) carboxamides. The reaction of nitrobenzene with urea anion in DMSO enabled one-pot synthesis of bis(4-nitrophenyl)amine
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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