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Publications in Math-Net.Ru |
Citations |
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2025 |
| 1. |
L. I. Minaeva, M. A. Topchiy, S. A. Rzhevskiy, A. F. Asachenko, “Pd-catalyzed isoprene telomerization with nucleophiles over the years: a look into the past and future prospects”, Mendeleev Commun., 35:6 (2025), 619–626  |
| 2. |
O. A. Zakurdaeva, A. F. Asachenko, M. A. Topchiy, S. V. Nesterov, “Effect of macrocycle stereoisomerism on extraction of Li<sup>+ </sup>cations from chloride media by solutions of dicyclohexano-14-crown-4 in 1,1,7-trihydrododecafluoroheptanol”, Mendeleev Commun., 35:3 (2025), 362–363   |
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2024 |
| 3. |
S. A. Rzhevskiy, O. V. Shurupova, A. F. Asachenko, N. M. Belov, A. V. Plutalova, E. S. Trofimchuk, R. V. Toms, E. V. Chernikova, I. P. Beletskaya, “Polymerization–cyclodepolymerization of polypropylene carbonate mediated by cobalt catalyst”, Mendeleev Commun., 34:6 (2024), 878–880 |
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| 4. |
O. V. Samsonov, G. P. Goryunov, D. V. Uborsky, A. F. Asachenko, J. A. M. Canich, J. Yang, A. Z. Voskoboynikov, “Sulfur-bridged bis(2-indenyl) zirconocenes and their performance in olefin polymerization”, Mendeleev Commun., 34:6 (2024), 815–818 |
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2023 |
| 5. |
E. A. Golubeva, M. I. Lavrov, P. N. Veremeeva, E. M. Bovina, E. V. Radchenko, M. A. Topchiy, A. F. Asachenko, V. L. Zamoyski, V. V. Grigoriev, V. A. Palyulin, “New 1,11-dimethyl-3,6,9-triazatricyclo[7.3.1.1<sup>3,11</sup>]tetradecane-4,8,12-trione derivative as an allosteric modulator of the glutamatergic system”, Mendeleev Commun., 33:1 (2023), 70–72 |
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2022 |
| 6. |
O. V. Shurupova, G. K. Sterligov, M. A. Rasskazova, E. A. Drokin, A. N. Lysenko, S. A. Rzhevskiy, L. I. Minaeva, M. A. Topchiy, A. F. Asachenko, “One-pot two step synthesis of unsymmetrically substituted indenes from 3,4-diarylbutadiene sulfones”, Mendeleev Commun., 32:4 (2022), 446–448 |
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| 7. |
S. A. Rzhevskiy, M. A. Topchiy, V. N. Bogachev, L. I. Minaeva, I. R. Cherkashchenko, K. V. Lavrov, G. K. Sterligov, M. S. Nechaev, A. F. Asachenko, “Solvent-free palladium-catalyzed C–O cross-coupling of (hetero)aryl halides with primary alcohols”, Mendeleev Commun., 32:2 (2022), 258–259 |
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2021 |
| 8. |
S. A. Rzhevskiy, V. N. Bogachev, L. I. Minaeva, G. K. Sterligov, M. S. Nechaev, M. A. Topchiy, A. F. Asachenko, “Efficient synthesis of 3-arylbutadiene sulfones using the Heck–Matsuda reaction”, Mendeleev Commun., 31:4 (2021), 548–549 |
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| 9. |
S. A. Rzhevskiy, M. A. Topchiy, V. N. Bogachev, A. A. Ageshina, L. I. Minaeva, G. K. Sterligov, M. S. Nechaev, A. F. Asachenko, “NHC Pd<sup>ii</sup> complexes for the solvent-free telomerisation of isoprene with methanol”, Mendeleev Commun., 31:4 (2021), 478–480 |
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| 10. |
S. A. Rzhevskiy, M. A. Topchiy, V. N. Bogachev, L. I. Minaeva, I. R. Cherkashchenko, K. V. Lavrov, G. K. Sterligov, M. S. Nechaev, A. F. Asachenko, “Solvent-free palladium-catalyzed C–O cross-coupling of aryl bromides with phenols”, Mendeleev Commun., 31:3 (2021), 409–411 |
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| 11. |
P. S. Gribanov, D. A. Lypenko, A. V. Dmitriev, S. I. Pozin, M. A. Topchiy, A. F. Asachenko, D. A. Loginov, S. N. Osipov, “Synthesis and optical properties of novel unsymmetrically substituted benzothiadiazole-based luminophores”, Mendeleev Commun., 31:1 (2021), 33–35 |
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2020 |
| 12. |
M. A. Topchiy, S. A. Rzhevskiy, A. A. Ageshina, N. Yu. Kirilenko, G. K. Sterligov, D. Yu. Mladentsev, D. Yu. Parashchuk, S. N. Osipov, M. S. Nechaev, A. F. Asachenko, “Deep blue luminescent cyclometallated 1,2,3-triazol-5-ylidene iridium(<sc>iii</sc>) complexes”, Mendeleev Commun., 30:6 (2020), 717–718 |
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| 13. |
S. A. Rzhevskiy, M. A. Topchiy, Yu. D. Golenko, P. S. Gribanov, G. K. Sterligov, N. Yu. Kirilenko, A. A. Ageshina, M. V. Bermeshev, M. S. Nechaev, A. F. Asachenko, “Undirected ortho-selectivity in C–H borylation of arenes catalyzed by NHC platinum(0) complexes”, Mendeleev Commun., 30:5 (2020), 569–571 |
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2019 |
| 14. |
P. S. Gribanov, G. A. Chesnokov, P. B. Dzhevakov, N. Yu. Kirilenko, S. A. Rzhevskiy, A. A. Ageshina, M. A. Topchiy, M. V. Bermeshev, A. F. Asachenko, M. S. Nechaev, “Solvent-free Suzuki and Stille cross-coupling reactions of 4- and 5-halo-1,2,3-triazoles”, Mendeleev Commun., 29:2 (2019), 147–149 |
20
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| 15. |
M. A. Topchiy, P. B. Dzhevakov, N. Yu. Kirilenko, S. A. Rzhevskiy, A. A. Ageshina, V. N. Khrustalev, D. Yu. Parashchuk, M. V. Bermeshev, M. S. Nechaev, A. F. Asachenko, “Cyclometallated 1,2,3-triazol-5-ylidene iridium(III) complexes: synthesis, structure, and photoluminescence properties”, Mendeleev Commun., 29:2 (2019), 128–131 |
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2018 |
| 16. |
P. S. Gribanov, Yu. D. Golenko, M. A. Topchiy, A. N. Philippova, N. Yu. Kirilenko, N. V. Krivoshchapov, G. K. Sterligov, A. F. Asachenko, M. V. Bermeshev, M. S. Nechaev, “One-pot two-step stannylation/Stille homocoupling of aryl bromides and iodides under solvent-free conditions”, Mendeleev Commun., 28:3 (2018), 323–325 |
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2017 |
| 17. |
G. A. Chesnokov, P. S. Gribanov, M. A. Topchiy, L. I. Minaeva, A. F. Asachenko, M. S. Nechaev, E. V. Bermesheva, M. V. Bermeshev, “Solvent-free Buchwald–Hartwig amination with low palladium loadings”, Mendeleev Commun., 27:6 (2017), 618–620 |
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2016 |
| 18. |
A. V. Babkin, A. F. Asachenko, D. V. Uborsky, D. S. Kononovich, V. V. Izmer, V. A. Kudakina, V. A. Shnaider, N. E. Shevchenko, A. Z. Voskoboynikov, “Preparation of <i>N</i>-phenyl-<i>p</i>-phenylenediamine by coupling of aniline and nitrobenzene in KOH–poly(ethylene glycol) medium”, Mendeleev Commun., 26:6 (2016), 555–557 |
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2014 |
| 19. |
V. P. Ananikov, L. L. Khemchyan, Yu. V. Ivanova, V. I. Bukhtiyarov, A. M. Sorokin, I. P. Prosvirin, S. Z. Vatsadze, A. V. Medved'ko, V. N. Nuriev, A. D. Dilman, V. V. Levin, I. V. Koptyug, K. V. Kovtunov, V. V. Zhivonitko, V. A. Likholobov, A. V. Romanenko, P. A. Simonov, V. G. Nenajdenko, O. I. Shmatova, V. M. Muzalevskiy, M. S. Nechaev, A. F. Asachenko, O. S. Morozov, P. B. Dzhevakov, S. N. Osipov, D. V. Vorobyeva, M. A. Topchiy, M. A. Zotova, S. A. Ponomarenko, O. V. Borshchev, Yu. N. Luponosov, A. A. Rempel, A. A. Valeeva, A. Yu. Stakheev, O. V. Turova, I. S. Mashkovsky, S. V. Sysolyatin, V. V. Malykhin, G. A. Bukhtiyarova, A. O. Terent'ev, I. B. Krylov, “Development of new methods in modern selective organic synthesis: preparation of functionalized molecules with atomic precision”, Usp. Khim., 83:10 (2014), 885–985  ; Russian Chem. Reviews, 83:10 (2014), 885–985 |
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