Direct oxidative SNH amidation of 1,3,7-triazapyrene

Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/3733

Title:	Direct oxidative SNH amidation of 1,3,7-triazapyrene
Authors:	Borovlev, I. V. Боровлев, И. В. Demidov, O. P. Демидов, О. П. Kurnosova, N. A. Курносова, Н. А. Amangasieva, G. A. Амангазиева, Г. А. Avakyan, E. K. Авакян, Е. К.
Keywords:	1,3,7-triazapyrene;Nucleophilic substitution of hydrogen;Oxidative amidation
Issue Date:	2015
Publisher:	Springer New York LLC
Citation:	Borovlev, I.V., Demidov, O.P., Kurnosova, N.A., Amangasieva, G.A., Avakyan, E.K. Direct oxidative SNH amidation of 1,3,7-triazapyrene // Chemistry of Heterocyclic Compounds. - 2015. - Volume 51. - Issue 2. - Pages 170-175
Series/Report no.:	Chemistry of Heterocyclic Compounds
Abstract:	6-Acylamino-1,3,7-triazapyrenes have been synthesized for the first time by direct oxidative nucleophilic substitution of hydrogen
URI:	https://www.scopus.com/record/display.uri?eid=2-s2.0-84953356800&origin=resultslist&sort=plf-f&src=s&nlo=1&nlr=20&nls=afprfnm-t&affilName=north+caucasus+federal+university&sid=2b58301f3b6527e7b3146829ec448bcf&sot=afnl&sdt=cl&cluster=scopubyr%2c%222015%22%2ct&sl=53&s=%28AF-ID%28%22North+Caucasus+Federal+University%22+60070541%29%29&relpos=40&citeCnt=6&searchTerm= http://hdl.handle.net/20.500.12258/3733
Appears in Collections:	Статьи, проиндексированные в SCOPUS, WOS

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