Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12258/7499
Title: Nucleophilic addition of amide anions to 1-methyl-5(6,7,8)-nitroquinolinium salts
Authors: Avakyan, E. K.
Авакян, Е. К.
Amangasieva, G. A.
Амангазиева, Г. А.
Demidov, O. P.
Демидов, О. П.
Borovleva, A. A.
Боровлева, А. А.
Beketova, E. S.
Бекетова, Е. С.
Nechaeva, O. A.
Нечаева, О. А.
Borovlev, I. V.
Боровлев, И. В.
Keywords: Nitroquinoline N-methyl cations;Nitroquinolines;Nucleophilic addition
Issue Date: 2019
Publisher: Springer New York LLC
Citation: Avakyan, E.K., Amangasieva, G.А., Demidov, O.P., Borovleva, A.А., Beketova, E.S., Nechaeva, O.А., Borovlev, I.V. Nucleophilic addition of amide anions to 1-methyl-5(6,7,8)-nitroquinolinium salts // Chemistry of Heterocyclic Compounds. - 2019. - Volume 55. - Issue 8. - Pages 739-747
Series/Report no.: Chemistry of Heterocyclic Compounds
Abstract: The stable adducts, N-(1-methyl-5(6,7,8)-nitro-1,2-dihydroquinolin-2-yl)benzamides were synthesized for the first time by the action of amide anions of aromatic acids on the N-methyl salts of 5-, 6-, 7-, and 8-nitroquinolines in anhydrous MeCN. Oxidative dehydrogenation of these amides afforded aroylimino derivatives of the corresponding 1-methyl-5(6,7,8)-nitro-2-quinolones
URI: https://www.scopus.com/record/display.uri?eid=2-s2.0-85071603162&origin=resultslist&sort=plf-f&src=s&st1=Nucleophilic+addition+of+amide+anions+to+1-methyl-5+6%2c7%2c8-nitroquinolinium+salts&st2=&sid=1c5a6fe41babdcf93eed0c3d463275ee&sot=b&sdt=b&sl=95&s=TITLE-ABS-KEY%28Nucleophilic+addition+of+amide+anions+to+1-methyl-5+6%2c7%2c8-nitroquinolinium+salts%29&relpos=0&citeCnt=0&searchTerm=
http://hdl.handle.net/20.500.12258/7499
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

Files in This Item:
File Description SizeFormat 
scopusresults 1021 .pdf729.86 kBAdobe PDFThumbnail
View/Open
WoS 694 .pdf75.81 kBAdobe PDFThumbnail
View/Open


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