Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12258/2806
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
URI: https://www.scopus.com/record/display.uri?eid=2-s2.0-85050465848&origin=resultslist&sort=plf-f&src=s&nlo=&nlr=&nls=&sid=5f9b6becf5270e68a8c48a2159c718f9&sot=aff&sdt=sisr&sl=145&s=AF-ID%28%22North+Caucasus+Federal+University%22+60070541%29+OR+AF-ID%28%22%5bNo+Affiliation+ID+found%5d%22+60070961%29+OR+AF-ID%28%22%5bNo+Affiliation+ID+found%5d%22+60026323%29&ref=%28Synthesis+of+Amides+by+Nucleophilic+Substitution+of+Hydrogen+in+3-Nitropyridine%29&relpos=0&citeCnt=0&searchTerm=
http://hdl.handle.net/20.500.12258/2806
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