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Публикации в базе данных Math-Net.Ru |
Цитирования |
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2026 |
| 1. |
R. A. Irgashev, A. S. Steparuk, V. V. Emets, E. V. Tekshina, N. M. Tolkach, P. I. Lazarenko, G. L. Rusinov, S. A. Kozyukhin, “New metal-free dye with an acceptor-anchor group of thieno[3,2-<em>b</em>]thiophene family for dye-sensitized solar cells”, Mendeleev Commun., 36:1 (2026), 72–75  |
| 2. |
L. G. Samsonova, N. V. Izmailova, R. M. Gadirov, R. A. Irgashev, N. A. Kazin, Yu. A. Kvashnin, A. S. Steparuk, G. L. Rusinov, E. V. Verbitskiy, “Photoacid generation from substituted benzo[<em>b</em>]thiophene-2-carboxanilides”, Mendeleev Commun., 36:1 (2026), 50–52 |
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2023 |
| 3. |
Yu. A. Kvashnin, D. V. Belyaev, M. I. Kodess, M. A. Ezhikova, G. L. Rusinov, E. V. Verbitskiy, V. N. Charushin, “Two-step synthesis of indeno[1,2-b]furazanopyrazines through combination of the S<sub>N</sub><sup>H</sup> and Heck reactions”, Mendeleev Commun., 33:6 (2023), 753–755  |
4
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2022 |
| 4. |
E. V. Verbitskiy, Yu. A. Kvashnin, M. V. Medvedeva, T. S. Svalova, A. N. Kozitsina, O. S. Eltsov, G. L. Rusinov, V. N. Charushin, “First synthesis of new polycyclic systems from ortho-di(heteroaryl)-substituted furazanopyrazine derivatives by the Scholl reaction”, Mendeleev Commun., 32:6 (2022), 722–725 |
8
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| 5. |
A. S. Steparuk, R. A. Irgashev, E. F. Zhilina, V. V. Emets, V. A. Grinberg, E. V. Tekshina, E. V. Belova, P. I. Lazarenko, N. M. Tolkach, G. L. Rusinov, S. A. Kozyukhin, “New thieno[3,2-b]indole conjugates with 5-(methylene)rhodanine-3-acetic acid in dye-sensitized solar cells”, Mendeleev Commun., 32:4 (2022), 523–526 |
6
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2021 |
| 6. |
E. V. Verbitskiy, S. A. Baskakova, D. V. Belyaev, D. V. Vakhrusheva, N. I. Eremeeva, G. L. Rusinov, V. N. Charushin, “Renaissance of 4-(5-nitrofuran-2-yl)-5-arylamino substituted pyrimidines: microwave-assisted synthesis and antitubercular activity”, Mendeleev Commun., 31:2 (2021), 210–212 |
13
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2020 |
| 7. |
E. V. Verbitskiy, E. M. Dinastiya, O. S. Eltsov, E. F. Zhilina, A. V. Shchepochkin, G. L. Rusinov, O. N. Chupakhin, V. N. Charushin, “Assembly of annulated 1,3-diazapyrenes by consecutive cross-coupling and cyclodehydrogenation of (het)arene moieties”, Mendeleev Commun., 30:2 (2020), 142–144 |
13
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2019 |
| 8. |
D. V. Belyaev, D. L. Chizhov, M. I. Kodess, M. A. Ezhikova, G. L. Rusinov, V. N. Charushin, “Synthesis of 2-(polyfluoromethyl)pyrimido-[1,2-a]benzimidazole-4-carbaldehyde derivatives”, Mendeleev Commun., 29:3 (2019), 249–251 |
7
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| 9. |
I. G. Ovchinnikova, G. A. Kim, E. G. Matochkina, M. I. Kodess, E. V. Nosova, G. L. Rusinov, V. N. Charushin, “Pericyclic reactions in the synthesis of new 5-aryl-5,6-dihydroquinolino[2,1-b]quinazolin-12-ones”, Mendeleev Commun., 29:2 (2019), 135–137 |
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2018 |
| 10. |
Yu. A. Kvashnin, G. L. Rusinov, V. N. Charushin, “Metal-free protocol for the synthesis of novel 6-(het)aryl-5-aryl-5H-imidazo[4,5-b][1,2,5]oxadiazolo[3,4-e]pyrazines”, Mendeleev Commun., 28:5 (2018), 461–463 |
5
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| 11. |
E. V. Verbitskiy, S. A. Baskakova, N. A. Gerasimova, N. P. Evstigneeva, N. V. Zil'berberg, N. V. Kungurov, M. A. Kravchenko, G. L. Rusinov, O. N. Chupakhin, V. N. Charushin, “New 5-arylamino-4-(5-nitrofuran-2-yl)pyrimidines as promising antibacterial agents”, Mendeleev Commun., 28:4 (2018), 393–395 |
15
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| 12. |
O. V. Fedorova, Yu. A. Titova, I. G. Ovchinnikova, G. L. Rusinov, V. N. Charushin, “4-Hydroxyproline containing podands as new chiralcatalysts for the asymmetric Biginelli reaction”, Mendeleev Commun., 28:4 (2018), 357–358 |
17
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2016 |
| 13. |
A. V. Dmitriev, A. R. Yusupov, R. A. Irgashev, N. A. Kazin, E. I. Mal'tsev, D. A. Lypenko, G. L. Rusinov, A. V. Vannikov, V. N. Charushin, “Electron-hole mobility in 6,12-di(2-thienyl)indolo[3,2-b]carbazoles”, Mendeleev Commun., 26:6 (2016), 516–517 |
8
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2015 |
| 14. |
Ю. А. Титова, О. В. Федорова, Г. Л. Русинов, В. Н. Чарушин, “Оксиды металлов и кремния – эффективные катализаторы процессов препаративной органической химии”, Усп. хим., 84:12 (2015), 1294–1315  ; Yu. A. Titova, O. V. Fedorova, G. L. Rusinov, V. N. Charushin, “Metal and silicon oxides as efficient catalysts for the preparative organic chemistry”, Russian Chem. Reviews, 84:12 (2015), 1294–1315  |
15
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2009 |
| 15. |
G. L. Rusinov, E. V. Verbitskiy, P. A. Slepukhin, O. N. Zabelina, I. N. Ganebnykh, V. N. Kalinin, V. A. Ol'shevskaya, V. N. Charushin, “A new approach to incorporate the carboranyl fragment into 2,5-diazabicyclo[2.2.2]oct-2-enes”, Mendeleev Commun., 19:5 (2009), 243–245 |
9
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2006 |
| 16. |
G. L. Rusinov, P. A. Slepukhin, V. N. Charushin, O. A. Dyachenko, O. N. Kazheva, A. N. Chekhlov, E. V. Verbitskiy, M. I. Kodess, O. N. Chupakhin, “Chemistry of O- and C-adducts derived from 1,4-diazinium salts: the use of tetrahydropyrazines in the synthesis of condensed systems”, Mendeleev Commun., 16:1 (2006), 26–29 |
12
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| 17. |
A. Yu. Ponomareva, D. G. Beresnev, N. A. Itsikson, O. N. Chupakhin, G. L. Rusinov, “Synthesis of [2,3-b]thieno- and furoquinoxalines by the <mml:math altimg="si1.gif"><mml:mrow><mml:msubsup><mml:mtext>S</mml:mtext><mml:mtext>N</mml:mtext><mml:mtext>H</mml:mtext></mml:msubsup></mml:mrow></mml:math> and <mml:math altimg="si2.gif"><mml:mrow><mml:msubsup><mml:mtext>S</mml:mtext><mml:mtext>N</mml:mtext><mml:mrow><mml:mi>i</mml:mi><mml:mi>p</mml:mi><mml:mi>s</mml:mi><mml:mi>o</mml:mi></mml:mrow></mml:msubsup></mml:mrow></mml:math> reactions of 2-substituted quinoxalines with acetophenones”, Mendeleev Commun., 16:1 (2006), 16–18 |
10
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2002 |
| 18. |
I. P. Romanova, V. V. Kalinin, D. G. Yakhvarov, A. A. Nafikova, V. I. Kovalenko, P. V. Plekhanov, G. L. Rusinov, O. G. Sinyashin, “Synthesis and electrochemical properties of 2-(azahomo[60]fullereno)-5-nitropyrimidine”, Mendeleev Commun., 12:2 (2002), 51–52 |
12
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2001 |
| 19. |
G. L. Rusinov, P. A. Slepukhin, V. N. Charushin, O. N. Chupakhin, “2,3-Dichloro-1-alkylpyrazinium tetrafluoroborates: the synthesis and reactions with nucleophiles”, Mendeleev Commun., 11:2 (2001), 78–80 |
10
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2000 |
| 20. |
D. G. Beresnev, G. L. Rusinov, O. N. Chupakhin, H. Neunhoeffer, “Interaction of 5-methoxy-1,2,4-triazines with ureas as a new route to 6-azapurines”, Mendeleev Commun., 10:2 (2000), 58–59 |
7
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1999 |
| 21. |
G. L. Rusinov, P. V. Plekhanov, A. Yu. Ponomareva, O. N. Chupakhin, “First example of cine-substitution for halogens in azolopyrimidines”, Mendeleev Commun., 9:6 (1999), 233–234 |
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