Oxidative SNH amidation of acridine and tautomerism of N-(acridin-9-yl)benzamides

Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/3296

Title:	Oxidative SNH amidation of acridine and tautomerism of N-(acridin-9-yl)benzamides
Authors:	Demidov, O. P. Демидов, О. П. Borovlev, I. V. Боровлев, И. В. Amangasieva, G. A. Амангазиева, Г. А. Avakyan, E. K. Авакян, Е. К.
Keywords:	Acridine;Nucleophilic substitution of hydrogen;Oxidative amidation;Tautomerism
Issue Date:	2016
Publisher:	Springer New York LLC
Citation:	Demidov, O.P., Borovlev, I.V., Amangasieva, G.A., Avakyan, E.K. Oxidative SNH amidation of acridine and tautomerism of N-(acridin-9-yl)benzamides // Chemistry of Heterocyclic Compounds. - 2016. - Volume 52. - Issue 2. - Pages 104-109
Series/Report no.:	Chemistry of Heterocyclic Compounds
Abstract:	Direct oxidative nucleophilic substitution of hydrogen atom in acridine molecule was used to synthesize 9-acylaminoacridines. The prototropic amine-imine tautomerism of these compounds was studied
URI:	https://www.scopus.com/record/display.uri?eid=2-s2.0-84961771276&origin=resultslist&sort=plf-f&src=s&nlo=1&nlr=20&nls=afprfnm-t&affilName=north+caucasus+federal+university&sid=b34ee1a283c2e8415711b601b248f06f&sot=afnl&sdt=cl&cluster=scopubyr%2c%222016%22%2ct&sl=53&s=%28AF-ID%28%22North+Caucasus+Federal+University%22+60070541%29%29&relpos=79&citeCnt=4&searchTerm= http://hdl.handle.net/20.500.12258/3296
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