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Публикации в базе данных Math-Net.Ru |
Цитирования |
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2024 |
| 1. |
M. A. Novikov, K. V. Potapov, R. A. Novikov, P. N. Solyev, Yu. V. Tomilov, S. N. Kochetkov, A. A. Makarov, V. A. Mitkevich, “A convenient synthesis of a chlorobenzothiophenyl-indole-based inhibitor of bacterial cystathionine γ-lyase”, Mendeleev Commun., 34:2 (2024), 255–258  |
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2023 |
| 2. |
M. S. Novikov, M. P. Paramonova, I. M. Kirillov, O. A. Smirnova, A. L. Khandazhinskaya, A. O. Chizhov, S. N. Kochetkov, A. V. Ivanov, I. F. Fedyakina, “New N<sup>1</sup>-(4-aryloxybenzyl)uracils containing N<sup>3</sup>-positioned 4-(trimethyleneoxy)benzoic acid moiety, and study of their antiviral activity against SARS-CoV-2 and influenza virus”, Mendeleev Commun., 33:4 (2023), 537–538 |
1
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2022 |
| 3. |
S. D. Negrya, M. V. Jasko, D. A. Makarov, I. L. Karpenko, P. N. Solyev, V. O. Chekhov, O. V. Efremenkova, B. F. Vasilieva, T. A. Efimenko, S. N. Kochetkov, L. A. Alexandrova, “Oligoglycol carbonate prodrugs of 5-modified 2'-deoxyuridines: synthesis and antibacterial activity”, Mendeleev Commun., 32:4 (2022), 433–435 |
3
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2021 |
| 4. |
Е. С. Матюгина, С. Н. Кочетков, А. Л. Хандажинская, “Синтез и биологическая активность аза- и дезаза-аналогов пуриновых нуклеозидов”, Усп. хим., 90:11 (2021), 1454–1491  ; E. S. Matyugina, S. N. Kochetkov, A. L. Khandazhinskaya, “Synthesis and biological activity of aza and deaza analogues of purine nucleosides”, Russian Chem. Reviews, 90:11 (2021), 1454–1491   |
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2020 |
| 5. |
E. S. Matyugina, A. L. Khandazhinskaya, S. N. Kochetkov, K. L. Seley-Radtke, “Synthesis of 3-hetarylpyrroles by Suzuki–Miyaura cross-coupling”, Mendeleev Commun., 30:2 (2020), 231–232 |
10
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2019 |
| 6. |
M. A. Khomutov, A. O. Chizhov, S. N. Kochetkov, A. R. Khomutov, “Synthesis of (R)- and (S)-isomers of 2-methylspermidine”, Mendeleev Commun., 29:6 (2019), 678–679 |
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2018 |
| 7. |
M. A. Khomutov, M. T. Hyvönen, A. R. Simonian, J. Weisell, J. J. Vepsalainen, L. Alhonen, S. N. Kochetkov, T. A. Keinanen, A. R. Khomutov, “Acetylated derivatives of C-methylated analogues of spermidine: synthesis and interaction with N<sup>1</sup>-acetylpolyamine oxidase”, Mendeleev Commun., 28:5 (2018), 479–481 |
5
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2017 |
| 8. |
M. S. Gaman, E. S. Matyugina, M. S. Novikov, D. A. Babkov, P. N. Solyev, S. N. Kochetkov, A. L. Khandazhinskaya, “New benzophenone phosphonate derivatives”, Mendeleev Commun., 27:4 (2017), 346–348 |
2
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2016 |
| 9. |
E. S. Matyugina, V. T. Valuev-Elliston, A. O. Chizhov, S. N. Kochetkov, A. L. Khandazhinskaya, “HIV-1 non-nucleoside reverse transcriptase inhibitors: incorporation of benzylphosphonate moiety for solubility improvement”, Mendeleev Commun., 26:2 (2016), 114–116 |
3
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2013 |
| 10. |
Э. Р. Шмаленюк, С. Н. Кочетков, Л. А. Александрова, “Новые ингибиторы роста Mycobacterium tuberculosis на основе модифицированных пиримидиновых нуклеозидов и их аналогов”, Усп. хим., 82:9 (2013), 896–915 ; E. R. Shmalenyuk, S. N. Kochetkov, L. A. Alexandrova, “New inhibitors of Mycobacterium tuberculosis growth based on modified pyrimidine nucleosides and their analogues”, Russian Chem. Reviews, 82:9 (2013), 896–915 |
27
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2012 |
| 11. |
Е. С. Матюгина, А. П. Хандажинская, С. Н. Кочетков, “Карбоциклические аналоги нуклеозидов: классификация, ферменты-мишени и механизмы действия, синтез”, Усп. хим., 81:8 (2012), 729–746 ; E. S. Matyugina, A. P. Khandazhinskaya, S. N. Kochetkov, “Carbocyclic nucleoside analogues: classification, target enzymes, mechanism of action and synthesis”, Russian Chem. Reviews, 81:8 (2012), 729–746 |
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