Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12258/7504
Title: S N H Amidation of nitroquinolines: synthesis of amides on the basis of nitro- and nitrosoquinolines
Authors: Amangasieva, G. A.
Амангазиева, Г. А.
Avakyan, E. K.
Авакян, Е. К.
Demidov, O. P.
Демидов, О. П.
Borovleva, A. A.
Боровлева, А. А.
Pobedinskaya, D. Y.
Побединская, Д. Ю.
Borovlev, I. V.
Боровлев, И. В.
Keywords: Disproportionation;N-(nitroquinolinyl)benzamides;N-(nitrosoquinolinyl)benzamides;Nitroquinolines;SN H amidation
Issue Date: 2019
Publisher: Springer New York LLC
Citation: Amangasieva, G.А., Avakyan, E.K., Demidov, O.P., Borovleva, A.A., Pobedinskaya, D.Y., Borovlev, I.V. S N H Amidation of nitroquinolines: synthesis of amides on the basis of nitro- and nitrosoquinolines // Chemistry of Heterocyclic Compounds. - 2019. - Volume 55. - Issue 7. - Pages 623-631
Series/Report no.: Chemistry of Heterocyclic Compounds
Abstract: Direct SN H amidation of 5-, 6-, 7-, and 8-nitroquinolines in anhydrous DMSO was used to obtain the respective aroylamino derivatives of nitro- and nitrosoquinolines
URI: https://www.scopus.com/record/display.uri?eid=2-s2.0-85070204638&origin=resultslist&sort=plf-f&src=s&st1=S+N+H+Amidation+of+nitroquinolines%3a+synthesis+of+amides+on+the+basis+of+nitro-+and+nitrosoquinolines&st2=&sid=1c5a6fe41babdcf93eed0c3d463275ee&sot=b&sdt=b&sl=115&s=TITLE-ABS-KEY%28S+N+H+Amidation+of+nitroquinolines%3a+synthesis+of+amides+on+the+basis+of+nitro-+and+nitrosoquinolines%29&relpos=0&citeCnt=1&searchTerm=
http://hdl.handle.net/20.500.12258/7504
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

Files in This Item:
File Description SizeFormat 
scopusresults 1026 .pdf907.8 kBAdobe PDFThumbnail
View/Open
WoS 682 .pdf75.18 kBAdobe PDFThumbnail
View/Open


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