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Публикации в базе данных Math-Net.Ru |
Цитирования |
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2025 |
| 1. |
Л. К. Садиева, К. В. Гржегоржевский, В. А. Платонов, С. Сантра, Г. В. Зырянов, В. Л. Русинов, “Ингибиторы “чувства кворума” растительного происхождения: взаимосвязь структура–активность”, Усп. хим., 94:11 (2025), RCR5192  ; L. K. Sadieva, K. V. Grzhegorzhevskii, V. A. Platonov, S. Santra, G. V. Zyryanov, V. L. Rusinov, “Quorum sensing inhibitors of plant origin: structure–activity relationships”, Russian Chem. Reviews, 94:11 (2025), RCR5192 |
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2024 |
| 2. |
I. I. Butorin, O. A. Konovalova, P. A. Slepukhin, S. K. Kotovskaya, V. L. Rusinov, “An alternative synthesis of 7-amino-6-nitro-substituted azolo[1,5-a]pyrimidines”, Mendeleev Commun., 34:5 (2024), 706–708  |
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2023 |
| 3. |
Д. Н. Ляпустин, В. В. Федотов, Е. Н. Уломский, В. Л. Русинов, О. Н. Чупахин, “Последние достижения в химии двухуглеродных нитросодержащих синтетических эквивалентов”, Усп. хим., 92:4 (2023), RCR5077 ; D. N. Lyapustin, V. V. Fedotov, E. N. Ulomsky, V. L. Rusinov, O. N. Chupakhin, “Recent advances in the chemistry of two-carbon nitro-containing synthetic equivalents”, Russian Chem. Reviews, 92:4 (2023), RCR5077  |
5
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2022 |
| 4. |
К. В. Саватеев, А. А. Спасов, В. Л. Русинов, “Малые синтетические молекулы с антигликирующей активностью. Соотношение “структура–активность””, Усп. хим., 91:6 (2022), RCR5041  ; K. V. Savateev, A. A. Spasov, V. L. Rusinov, “Small synthetic molecules with antiglycation activity. Structure–activity relationship”, Russian Chem. Reviews, 91:6 (2022), RCR5041 |
19
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2020 |
| 5. |
M. I. Savchuk, I. S. Kovalev, V. L. Rusinov, D. S. Kopchuk, A. P. Krinochkin, G. V. Zyryanov, O. N. Chupakhin, V. N. Charushin, “Rapid metal free construction of 3-positioned 2-pyridyl substituent in indoles”, Mendeleev Commun., 30:6 (2020), 712–713 |
7
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| 6. |
M. I. Savchuk, A. P. Krinochkin, A. Rammohan, A. F. Khasanov, D. S. Kopchuk, I. N. Egorov, S. Santra, G. V. Zyryanov, V. L. Rusinov, O. N. Chupakhin, “An expedient synthesis of 5-alkynyl-6-aryl-2,2′-bipyridines”, Mendeleev Commun., 30:5 (2020), 610–611 |
7
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| 7. |
V. L. Rusinov, R. A. Drokin, D. V. Tiufiakov, E. K. Voinkov, E. N. Ulomsky, “Synthesis and properties of the salts of 1-nitropropan-2-one and 1-nitrobutan-2-one”, Mendeleev Commun., 30:2 (2020), 177–179 |
5
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2018 |
| 8. |
К. В. Саватеев, Е. Н. Уломский, И. И. Буторин, В. Н. Чарушин, В. Л. Русинов, О. Н. Чупахин, “Азолоазины — антагонисты $\mathrm{A}_{2a}$-рецептора. Структура и свойства”, Усп. хим., 87:7 (2018), 636–669 ; K. V. Savateev, E. N. Ulomsky, I. I. Butorin, V. N. Charushin, V. L. Rusinov, O. N. Chupakhin, “Azoloazines as $\mathrm{A}_{2a}$ receptor antagonists. Structure–activity relationship”, Russian Chem. Reviews, 87:7 (2018), 636–669 |
32
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2017 |
| 9. |
E. K. Voinkov, E. N. Ulomsky, V. L. Rusinov, R. A. Drokin, V. V. Fedotov, E. B. Gorbunov, “1-Morpholino-2-nitroethylene as a precursor of nitroacetaldehyde in the synthesis of azolo[5,1-c][1,2,4]triazines”, Mendeleev Commun., 27:3 (2017), 285–286 |
14
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2016 |
| 10. |
N. V. Chepchugov, D. S. Kopchuk, I. S. Kovalev, G. V. Zyryanov, V. L. Rusinov, O. N. Chupakhin, “Convenient synthesis of α-dichloromethylpyridines from 3-trichloromethyl-1,2,4-triazines”, Mendeleev Commun., 26:3 (2016), 220–222 |
13
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| 11. |
E. K. Voinkov, E. N. Ulomsky, V. L. Rusinov, K. V. Savateev, V. V. Fedotov, E. B. Gorbunov, M. L. Isenov, O. S. Eltsov, “New stable form of nitroacetonitrile”, Mendeleev Commun., 26:2 (2016), 172–173 |
18
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2015 |
| 12. |
A. F. Khasanov, D. S. Kopchuk, I. S. Kovalev, O. S. Taniya, G. V. Zyryanov, V. L. Rusinov, O. N. Chupakhin, “Reaction of lithium 2-arylethynides with 6-aryl-3-(2-pyridyl)-1,2,4-triazines as an access to 6-aryl-5-arylvinyl-3-(2-pyridyl)-1,2,4-triazines”, Mendeleev Commun., 25:5 (2015), 332–333 |
12
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| 13. |
D. S. Kopchuk, I. L. Nikonov, G. V. Zyryanov, E. V. Nosova, I. S. Kovalev, P. A. Slepukhin, V. L. Rusinov, O. N. Chupakhin, “Aryne approach towards 2,3-difluoro-10-(1H-1,2,3-triazol-1-yl)pyrido[1,2-a]indoles”, Mendeleev Commun., 25:1 (2015), 13–14 |
20
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| 14. |
И. С. Ковалев, Д. С. Копчук, Г. В. Зырянов, В. Л. Русинов, О. Н. Чупахин, В. Н. Чарушин, “Литийорганические соединения в реакциях нуклеофильного замещения атома водорода в ряду аренов и гетаренов”, Усп. хим., 84:12 (2015), 1191–1225 ; I. S. Kovalev, D. S. Kopchuk, G. V. Zyryanov, V. L. Rusinov, O. N. Chupakhin, V. N. Charushin, “Organolithium compounds in the nucleophilic substitution of hydrogen in arenes and hetarenes”, Russian Chem. Reviews, 84:12 (2015), 1191–1225 |
28
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2014 |
| 15. |
I. S. Kovalev, D. S. Kopchuk, A. F. Khasanov, G. V. Zyryanov, V. L. Rusinov, O. N. Chupakhin, “The synthesis of polyarene-modified 5-phenyl-2,2'-bipyridines via the $\mathrm{S_N^H}$ methodology and aza-Diels–Alder reaction”, Mendeleev Commun., 24:2 (2014), 117–118 |
29
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| 16. |
I. S. Kovalev, D. S. Kopchuk, G. V. Zyryanov, V. L. Rusinov, O. N. Chupakhin, “Nucleophilic dimerization of indoline under oxidative conditions”, Mendeleev Commun., 24:1 (2014), 40–41 |
2
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| 17. |
Г. В. Зырянов, Д. С. Копчук, И. С. Ковалев, Э. В. Носова, В. Л. Русинов, О. Н. Чупахин, “Хемосенсоры для обнаружения нитроароматических (взрывчатых) веществ”, Усп. хим., 83:9 (2014), 783–819 ; G. V. Zyryanov, D. S. Kopchuk, I. S. Kovalev, E. V. Nosova, V. L. Rusinov, O. N. Chupakhin, “Chemosensors for detection of nitroaromatic compounds (explosives)”, Russian Chem. Reviews, 83:9 (2014), 783–819 |
87
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2013 |
| 18. |
D. S. Kopchuk, A. F. Khasanov, I. S. Kovalev, G. V. Zyryanov, V. L. Rusinov, O. N. Chupakhin, “Unexpected reduction of the nitro group in (3-nitrophenyl)-1,2,4-triazines during their aza-Diels–Alder reaction with 1-morpholinocyclopentene”, Mendeleev Commun., 23:4 (2013), 209–211 |
22
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| 19. |
D. S. Kopchuk, I. S. Kovalev, A. F. Khasanov, G. V. Zyryanov, P. A. Slepukhin, V. L. Rusinov, O. N. Chupakhin, “A rational protocol for the synthesis of 1-(2-pyridyl)isoquinolines”, Mendeleev Commun., 23:3 (2013), 142–144 |
19
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2008 |
| 20. |
I. N. Egorov, B. König, V. L. Rusinov, O. N. Chupakhin, “Diastereoselective synthesis of 3-substituted acylamino-3,4-dihydro-1,2,4-triazinones”, Mendeleev Commun., 18:2 (2008), 99–101 |
7
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2005 |
| 21. |
D. N. Kozhevnikov, N. N. Kataeva, V. L. Rusinov, O. N. Chupakhin, G. G. Alexandrov, “Transformations of 1,2,4-triazine 4-oxides to pyridazines and triazolo[4,3-b]pyridazines by the action of substituted acetonitriles”, Mendeleev Commun., 15:1 (2005), 31–33 |
9
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| 22. |
V. N. Kozhevnikov, O. V. Shabunina, A. R. Sharifullina, V. L. Rusinov, O. N. Chupakhin, B. König, “Aminomethyl bi- and terpyridines as luminescent probes for Zn<sup>2+</sup> ions”, Mendeleev Commun., 15:1 (2005), 8–9 |
10
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| 23. |
V. N. Kozhevnikov, D. N. Kozhevnikov, O. V. Shabunina, V. L. Rusinov, O. N. Chupakhin, M. Zabel, B. König, “Synthesis, structure and luminescence of ruthenium complexes with 6-cyano-2,2'-bipyridines”, Mendeleev Commun., 15:1 (2005), 6–8 |
1
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| 24. |
И. Н. Егоров, Г. В. Зырянов, В. Л. Русинов, О. Н. Чупахин, “Асимметрическая индукция в реакциях нуклеофильного присоединения в ряду ароматических азинов”, Усп. хим., 74:12 (2005), 1176–1192 ; I. N. Egorov, G. V. Zyryanov, V. L. Rusinov, O. N. Chupakhin, “Asymmetric induction in the nucleophilic addition in the series of aromatic azines”, Russian Chem. Reviews, 74:12 (2005), 1073–1087 |
12
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2003 |
| 25. |
O. N. Chupakhin, A. M. Prokhorov, D. N. Kozhevnikov, V. L. Rusinov, V. N. Kalinin, V. A. Ol'shevskaya, I. V. Glukhov, M. Yu. Antipin, “1,2,4-Triazinylcarboranes: a new approach to the synthesis and the crystal structures of 1-(3,6-ditolyl-1,2,4-triazin-5-yl)-2-phenyl-1,2-dicarba-closo-dodecaborane and 1,7-bis[6-phenyl-3-(4-chlorophenyl)-1,2,4-triazin-5-yl]-1,7-dicarba-closo-dodecaborane”, Mendeleev Commun., 13:4 (2003), 165–167 |
15
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2002 |
| 26. |
D. N. Kozhevnikov, V. N. Kozhevnikov, T. V. Nikitina, V. L. Rusinov, O. N. Chupakhin, H. Neunhoeffer, “Synthesis of functionalised bipyridines by sequential nucleophilic substitution of hydrogen and cycloaddition in 1,2,4-triazine rings”, Mendeleev Commun., 12:1 (2002), 30–32 |
11
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2001 |
| 27. |
O. N. Chupakhin, V. L. Rusinov, G. V. Zyryanov, “Regioselectivity in the reactions of pyrroles with 3-aryl-1,2,4-triazin-5-ones”, Mendeleev Commun., 11:2 (2001), 77–78 |
3
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2000 |
| 28. |
I. S. Kovalev, D. N. Kozhevnikov, V. L. Rusinov, O. N. Chupakhin, D. V. Raikov, V. A. Pustovarov, B. V. Shulgin, “Direct introduction of indoles into 2-aminopyrazine 1-oxides”, Mendeleev Commun., 10:6 (2000), 229–230 |
6
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| 29. |
D. N. Kozhevnikov, A. M. Prokhorov, V. L. Rusinov, O. N. Chupakhin, “Auto-aromatization of the σ<sup>H</sup>-adducts of 1,2,4-triazine 4-oxides with carbanions in reactions of nucleophilic substitution of hydrogen”, Mendeleev Commun., 10:6 (2000), 227–228 |
7
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| 30. |
D. N. Kozhevnikov, T. V. Nikitina, V. L. Rusinov, O. N. Chupakhin, “The Ritter reaction in the 5-cyano-1,2,4-triazine series”, Mendeleev Commun., 10:3 (2000), 117–118 |
7
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1999 |
| 31. |
V. V. Voronin, E. N. Ulomsky, V. L. Rusinov, O. N. Chupakhin, “Regiospecific cleavage of a triazole or pyrimidine ring in nitrotriazolo[1,5-a]pyrimidones”, Mendeleev Commun., 9:5 (1999), 200–201 |
3
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1998 |
| 32. |
Д. Н. Кожевников, В. Л. Русинов, О. Н. Чупахин, “1,2,4-Триазин-N-оксиды и их аннелированные производные”, Усп. хим., 67:8 (1998), 707–722 ; D. N. Kozhevnikov, V. L. Rusinov, O. N. Chupakhin, “1,2,4-Triazine N-oxides and their annelated derivatives”, Russian Chem. Reviews, 67:8 (1998), 633–648 |
31
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1997 |
| 33. |
D. N. Kozhevnikov, V. N. Kozhevnikov, V. L. Rusinov, O. N. Chupakhin, “A general method for the synthesis of 1,2,4-triazine 4-oxides”, Mendeleev Commun., 7:6 (1997), 238–239 |
14
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| 34. |
D. N. Kozhevnikov, E. N. Ulomsky, V. L. Rusinov, O. N. Chupakhin, H. Neunhoeffer, “Stable σ-adducts of 6-phenyl-1,2,4-triazine 4-oxides with phenols”, Mendeleev Commun., 7:3 (1997), 116–117 |
7
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| 35. |
O. N. Chupakhin, V. L. Rusinov, E. N. Ulomsky, D. N. Kozhevnikov, H. Neunhoeffer, “Nucleophilic substitution of hydrogen in the reaction of 1,2,4-triazine-4-oxides with cyanides”, Mendeleev Commun., 7:2 (1997), 66–67 |
24
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1996 |
| 36. |
D. N. Kojevnikov, V. L. Rusinov, E. N. Ulomsky, O. N. Chupakhin, H. Neunhoeffer, “Extensive degradation of the heterocyclic system in the reaction of l,2,4-triazolo[5,l-c]triazin-7(4H)-ones with resorcinol and its derivatives”, Mendeleev Commun., 6:4 (1996), 152–153 |
3
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1994 |
| 37. |
Yu. A. Azev, I. P. Loginova, O. L. Guselnikova, S. V. Shorshnev, V. L. Rusinov, O. N. Chupakhin, “Reactions of Diazido Derivatives of s-Triazine with C-Nucleophiles”, Mendeleev Commun., 4:3 (1994), 104–107 |
7
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1993 |
| 38. |
V. L. Rusinov, M. N. Kushnir, O. N. Chupakhin, G. G. Alexandrov, “Reaction of 6-Nitro-1,2,4-triazolo[1,5-a]pyrimidines with Benzylamine: an Unusual Synthesis of 1-Hydroxyimidazoles”, Mendeleev Commun., 3:5 (1993), 213–214 |
6
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| 39. |
Yu. A. Azev, I. P. Loginova, O. L. Guselnikova, S. V. Shorshnev, N. A. Klyuev, V. L. Rusinov, O. N. Chupakhin, “Transformation of Azido Derivatives of s-Triazine into 1,2,4-Triazolylaminotetrazoles”, Mendeleev Commun., 3:2 (1993), 49–50 |
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