Zobrazeno 1 - 6
of 6
pro vyhledávání: '"nitro group transformations"'
Autor:
Artyom O. Neymash, Evgeny N. Ulomsky, Victor V. Fedotov, Semen V. Aminov, Daniil N. Lyapustin, Evgeny B. Gorbunov, Vladislav A. Ishimnikov, Pavel A. Slepukhin, Vladimir L. Rusinov
Publikováno v:
Molecules, Vol 29, Iss 1, p 134 (2023)
A fundamentally new synthetic approach to the synthesis of 2-aminopurine has been developed. It consists in the combination of the creation of a condensed polyazotic heterocyclic tetrazolopyrimidine structure, its transformation into triaminopyrimidi
Externí odkaz:
https://doaj.org/article/9e98e5044687470c967180099ed86538
Akademický článek
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Autor:
Alexandra Ivoilova, Ludmila V. Mikhalchenko, Anton Tsmokalyuk, Marina Leonova, Andrey Lalov, Polina Mozharovskaia, Alisa N. Kozitsina, Alla V. Ivanova, Vladimir L. Rusinov
Publikováno v:
Molecules, Vol 26, Iss 16, p 5087 (2021)
This article presents the results of a study of electrochemical transformations in aqueous and aprotic media of 5-methyl-6-nitro-7-oxo-4,7-dihydro-1,2,4-triazolo[1,5-a]pyrimidinide l-arginine monohydrate (1a, Triazid) obtained by electrochemical meth
Externí odkaz:
https://doaj.org/article/e30b1879d52f4964a4ee93268aa1c258
Autor:
A. N. Kozitsina, Andrey V. Lalov, A. V. Ivanova, A. N. Tsmokalyuk, Marina Yu. Leonova, L. V. Mikhal’chenko, Polina Mozharovskaia, Vladimir L. Rusinov, Alexandra Ivoilova
Publikováno v:
Molecules
Molecules, Vol 26, Iss 5087, p 5087 (2021)
Volume 26
Issue 16
Molecules, Vol 26, Iss 5087, p 5087 (2021)
Volume 26
Issue 16
This article presents the results of a study of electrochemical transformations in aqueous and aprotic media of 5-methyl-6-nitro-7-oxo-4,7-dihydro-1,2,4-triazolo[1,5-a]pyrimidinide l-arginine monohydrate (1a, Triazid) obtained by electrochemical meth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa4ece3d5e23c37b4efd6edb1f768960
http://europepmc.org/articles/PMC8400642
http://europepmc.org/articles/PMC8400642
Akademický článek
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Autor:
Neymash AO; Chemical Engineering Institute, Ural Federal University, 19 Mira St., 620002 Yekaterinburg, Russia., Ulomsky EN; Chemical Engineering Institute, Ural Federal University, 19 Mira St., 620002 Yekaterinburg, Russia., Fedotov VV; Chemical Engineering Institute, Ural Federal University, 19 Mira St., 620002 Yekaterinburg, Russia., Aminov SV; Chemical Engineering Institute, Ural Federal University, 19 Mira St., 620002 Yekaterinburg, Russia., Lyapustin DN; Chemical Engineering Institute, Ural Federal University, 19 Mira St., 620002 Yekaterinburg, Russia., Gorbunov EB; Institute of Organic Synthesis, Ural Branch of the Russian Academy of Science, Sofii Kovalevskoy St. 22, 620137 Yekaterinburg, Russia., Ishimnikov VA; Chemical Engineering Institute, Ural Federal University, 19 Mira St., 620002 Yekaterinburg, Russia., Slepukhin PA; Institute of Organic Synthesis, Ural Branch of the Russian Academy of Science, Sofii Kovalevskoy St. 22, 620137 Yekaterinburg, Russia., Rusinov VL; Chemical Engineering Institute, Ural Federal University, 19 Mira St., 620002 Yekaterinburg, Russia.
Publikováno v:
Molecules (Basel, Switzerland) [Molecules] 2023 Dec 25; Vol. 29 (1). Date of Electronic Publication: 2023 Dec 25.