Nucleophilic substitution of nitro group in dihydroazole[5,1-c] [1,2,4]triazines

Please use this identifier to cite or link to this item: http://elar.urfu.ru/handle/10995/103320

Title:	Nucleophilic substitution of nitro group in dihydroazole[5,1-c] [1,2,4]triazines
Authors:	Voinkov, E. K. Drokin, R. A. Tufyakov, D. V. Ulomsky, E. N. Rusinov, V. L.
Issue Date:	2020
Publisher:	American Institute of Physics Inc.
Citation:	Nucleophilic substitution of nitro group in dihydroazole[5,1-c] [1,2,4]triazines / E. K. Voinkov, R. A. Drokin, D. V. Tufyakov, et al. — DOI 10.1063/5.0018191 // AIP Conference Proceedings. — 2020. — Vol. 2280. — 0018191.
Abstract:	In the present work, we report the structural analogs of the antiviral drug Triazavirin. We carry out a study of nucleophilic substitution reaction of the nitro group in azolo[5,1-c][1,2,4]triazines with various aromatic amines and a hydrazine derivative. © 2020 Author(s).
URI:	http://elar.urfu.ru/handle/10995/103320
Access:	info:eu-repo/semantics/openAccess
SCOPUS ID:	85096433219
WOS ID:	000598468000045
PURE ID:	013ae271-0f50-4430-86c6-0cab69602a92 20127498
ISSN:	0094243X
ISBN:	9780735440104
DOI:	10.1063/5.0018191
metadata.dc.description.sponsorship:	The work was supported by the Russian Foundation for Basic Research (project № 19-33-90086).
Appears in Collections:	Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC

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