Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/3444
Title: SN H arylamination of nitroquinolines: access to nitro and nitroso derivatives of arylaminoquinolines
Authors: Demidov, O. P.
Демидов, О. П.
Pobedinskaya, D. Y.
Побединская, Д. Ю.
Avakyan, E. K.
Авакян, Е. К.
Amangasieva, G. A.
Амангазиева, Г. А.
Borovlev, I. V.
Боровлев, И. В.
Keywords: Disproportionation;Nitroquinolines;Phenazines;SN H arylamination;SN H methodology
Issue Date: 2018
Publisher: Springer New York LLC
Citation: Demidov, O.P., Pobedinskaya, D.Y., Avakyan, E.K., Amangasieva, G.A., Borovlev, I.V. SN H Arylamination of Nitroquinolines: Access to Nitro and Nitroso Derivatives of Arylaminoquinolines // Chemistry of Heterocyclic Compounds. - 2018. - Volume 54. - Issue 9. - Pages 875-886
Series/Report no.: Chemistry of Heterocyclic Compounds
Abstract: SN H Arylamination of 5-, 6-, 7-, and 8-nitroquinolines in anhydrous DMSO gave not only the arylamino derivatives of the respective nitroquinolines, but also the arylamino derivatives of nitrosoquinolines. In the case of 6-nitroquinoline, the first representatives of polycyclic structures on the basis of pyrido[3,2-a]phenazine 7-oxide were isolated
URI: https://www.scopus.com/record/display.uri?eid=2-s2.0-85055981821&origin=resultslist&sort=plf-f&src=s&nlo=1&nlr=20&nls=afprfnm-t&affilName=north+caucasus+federal+university&sid=1f180307c145020403eeb63cdb0265e9&sot=afnl&sdt=sisr&sl=53&s=%28AF-ID%28%22North+Caucasus+Federal+University%22+60070541%29%29&ref=%28Arylamination+of+Nitroquinolines%3a+Access+to+Nitro+and+Nitroso+Derivatives+of+Arylaminoquinolines%29&relpos=0&citeCnt=0&searchTerm=
http://hdl.handle.net/20.500.12258/3444
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