Zobrazeno 1 - 10
of 38
pro vyhledávání: '"E. N. Ulomskii"'
Publikováno v:
Chimica Techno Acta, Vol 2, Iss 3, Pp 234-246 (2015)
Chimica Techno Acta; Том 2, № 3 (2015); 234-246
Chimica Techno Acta; Том 2, № 3 (2015); 234-246
As a model of metabolic transformations of antiviral drug “Triazaverin” and its analogues‑2-alkylthio‑6-nitro‑1,2,4-triazolo[5,1-c][1,2,4]triazine‑7-ones 1a-d examined the oxidation of alkylthio groups to the corresponding sulfoxides 2a-d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42c48fa53ee9f79bf91463556ada363f
https://journals.urfu.ru/index.php/chimtech/article/view/1281
https://journals.urfu.ru/index.php/chimtech/article/view/1281
Autor:
Gennady L. Rusinov, Maksim L. Isenov, Evgeny B. Gorbunov, E. N. Ulomskii, Valery N. Charushin
Publikováno v:
Chemistry of Heterocyclic Compounds. 51:491-495
6-Nitroazolo[1,5-а]pyrimidines were used as dipolarophiles in a reaction with sodium azide providing previously unknown 2Н-azolo[1,5-а]-[1,2,3]triazolo[4,5-е]pyrimidines.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77d51d71502473d50fa63d7ecbc376e7
https://doi.org/10.1007/s10593-015-1725-2
https://doi.org/10.1007/s10593-015-1725-2
Autor:
Oleg N. Chupakhin, E. N. Ulomskii, Igor A. Khalymbadzha, G. L. Rusinov, Vladimir L. Rusinov, O. S. El´tsov, Victor G. Kartsev, Evgeny B. Gorbunov, V. N. Charushin
Publikováno v:
Chem. Nat. Compd.
Chemistry of Natural Compounds
Chemistry of Natural Compounds
The work was sponsored by the Russian Science Foundation (Project 14-13-01301).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec4555ca7a1d46d48b413f913de949af
https://doi.org/10.1007/s10600-016-1749-6
https://doi.org/10.1007/s10600-016-1749-6
Autor:
A. N. Korovina, Inna L. Karpenko, T. S. Shestakova, Galegov Ga, V.L. Andronova, Vladimir L. Rusinov, Oleg N. Chupakhin, Anastasia L. Khandazhinskaya, Marina K. Kukhanova, Sergey L. Deev, Maxim V. Yasko, E. N. Ulomskii
Publikováno v:
Bioorganic Chemistry. 38:265-270
A new class of inhibitors of herpes simplex virus replication was found. The compounds under study are derived from condensed 1,2,4-triazolo[5,1-c][1,2,4]triazines and 1,2,4-triazolo[1,5-a]pyrimidines, structural analogues of natural nucleic bases. A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b22e0215b960ab401eaeef6ded33dd0c
https://doi.org/10.1016/j.bioorg.2010.09.002
https://doi.org/10.1016/j.bioorg.2010.09.002
Autor:
S. L. Deev, T. S. Shestakova, Oleg I. Kiselev, Rusinova Larisa I, E. G Deeva, O. N. Chupakhin, E. N. Ulomskii, Vladimir L. Rusinov
Publikováno v:
Russian Chemical Bulletin. 59:136-143
Nucleoside analogs containing hydroxybutyl, hydroxyethoxymethyl, allyloxymethyl, and propargyloxymethyl fragments were synthesized based on 1,2,4-triazolo[3,2-c][1,2,4]triazin-7-ones isosteric to purine bases. Some of the compounds obtained inhibit i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a07b320aeda3e9bd90e979c971c8318c
https://doi.org/10.1007/s11172-010-0056-9
https://doi.org/10.1007/s11172-010-0056-9
Autor:
V. I. Saloutin, M. V. Pryadeina, Ya. V. Burgart, E. N. Ulomskii, Pavel A. Slepukhin, E. V. Sadchikova
Publikováno v:
Russian Journal of Organic Chemistry. 45:242-247
Methods were developed of the synthesis of alkyl 2-hydroxy-2-fluoroalkyl-4-phenyl-1,2,3,4—tetrahydroimidazo-[1,5-a]pyrimidine-3-carboxylates and alkyl-5-hydroxy-2,7-diphenyl-5-fluoroalkyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine-6-carboxylates b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::748872bd3b4735038aaf8cb11a05f9d5
https://doi.org/10.1134/s1070428009020158
https://doi.org/10.1134/s1070428009020158
Publikováno v:
Russian Chemical Bulletin. 57:985-1014
Synthetic methods, reactivity, and the properties of a new class of antiviral compounds, pyrazolo-, imidazo-, 1,2,4-triazolo[5,1-c]-1,2,4-triazinones, tetrazolo[5,1-b]-1,2,4-triazinones, and azoloannulated amino-1,2,4-triazines having structural simi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ead5863b4644c072da657e6b4829f071
https://doi.org/10.1007/s11172-008-0130-8
https://doi.org/10.1007/s11172-008-0130-8
Autor:
Maksim L. Isenov, Gennady L. Rusinov, Valery N. Charushin, E. N. Ulomskii, Evgeny B. Gorbunov
Publikováno v:
ChemInform. 46
Title compounds are conveniently and in high yields synthesized by a regioselective reaction from 6-nitroazolo[1,5-a]pyrimidines with sodium azide.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::81fc4f1eba474f24bde5eef7887f93fd
https://doi.org/10.1002/chin.201549177
https://doi.org/10.1002/chin.201549177
Publikováno v:
Russian Chemical Bulletin. 54:726-732
A new in principle method for the synthesis of 6-aryl(hetaryl)-3,5-diamino-1,2,4-triazines by decomposition of pre-synthesized tetrazolo[1,5-b][1,2,4]triazines was developed. The advantages of this method over traditional methods were demonstrated us
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22e26c3908d7ac1b475ab5ed8093fc32
https://doi.org/10.1007/s11172-005-0311-7
https://doi.org/10.1007/s11172-005-0311-7
Autor:
V. I. Saloutin, M. I. Kodess, Ya. V. Burgart, E. N. Ulomskii, M. V. Pryadeina, Vladimir L. Rusinov
Publikováno v:
Russian Journal of Organic Chemistry. 40:902-907
Fluorinated 3-oxo esters react with aldehydes and 3-amino-1,2,4-triazoles and 5-aminotetrazoles to give, respectively, 7-alkyl(aryl)-6-alkoxycarbonyl-5-fluoroalkyl-1,2,4-triazolo[1,5-a]pyrimidines and -tetra-zolo[1,5-a]pyrimidines. The same heterocyc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffd30d834c401250a02e7a5df0d97656
https://doi.org/10.1023/b:rujo.0000044558.47152.65
https://doi.org/10.1023/b:rujo.0000044558.47152.65