Urea in an aminodemethoxylation reaction of 6-methoxy-1,3,7-triazapyrenes

Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/3709

Title:	Urea in an aminodemethoxylation reaction of 6-methoxy-1,3,7-triazapyrenes
Authors:	Amangasieva, G. A. Амангазиева, Г. А. Borovlev, I. V. Боровлев, И. В. Demidov, O. P. Демидов, О. П. Kurnosova, N. A. Курносова, Н. А. Avakyan, E. K. Авакян, Е. К.
Keywords:	6-methoxy-1,3,7-triazapyrenes;Nucleophilic ipso substitution of methoxy group;Urea
Issue Date:	2015
Publisher:	Springer New York LLC
Citation:	Amangasieva, G.A., Borovlev, I.V., Demidov, O.P., Kurnosova, N.A., Avakyan, E.K. Urea in an aminodemethoxylation reaction of 6-methoxy-1,3,7-triazapyrenes // Chemistry of Heterocyclic Compounds. - 2015. - Volume 51. - Issue 6. - Pages 586-588
Series/Report no.:	Chemistry of Heterocyclic Compounds
Abstract:	Upon reaction of N-anion of urea with 6-methoxy-1,3,7-triazapyrenes in DMSO at room temperature the products of nucleophilic ipso substitution of methoxy group with amino group form in high yields
URI:	https://www.scopus.com/record/display.uri?eid=2-s2.0-84938974457&origin=resultslist&sort=plf-f&src=s&nlo=1&nlr=20&nls=afprfnm-t&affilName=north+caucasus+federal+university&sid=c73d1c358909356c25b8ba1aa4ce585d&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=23&citeCnt=2&searchTerm= http://hdl.handle.net/20.500.12258/3709
Appears in Collections:	Статьи, проиндексированные в SCOPUS, WOS

Files in This Item:

File	Description	Size	Format
scopusresults 676 .pdf Restricted Access		64.14 kB	Adobe PDF	View/Open
WoS 439 .pdf Restricted Access		187.5 kB	Adobe PDF	View/Open

Репозиторий научных и учебно-методических публикаций