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Publications in Math-Net.Ru |
Citations |
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2025 |
| 1. |
E. N. Shepelenko, V. A. Podshibyakin, O. P. Demidov, K. E. Shepelenko, V. M. Chernyshev, “Synthetic protocol for the preparation of new ([2,2':6',2"-terpyridin]-4'-yl)naphthalene derivatives”, Mendeleev Commun., 35:1 (2025), 96–98  |
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2024 |
| 2. |
N. I. Vikrishchuk, O. P. Demidov, O. I. Askalepova, L. D. Popov, Yu. I. Ryabukhin, “Crystal structure and properties of new benzimidazopyrido[2,3-<i>b</i>]indole-6-carbonitriles”, Mendeleev Commun., 34:2 (2024), 274–276 |
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2023 |
| 3. |
A. A. Zubenko, L. N. Divaeva, A. S. Morkovnik, V. S. Sochnev, O. P. Demidov, V. V. Chekrysheva, A. I. Klimenko, A. E. Svyatogorova, “β-Carbolines as intermediates in indirect heteroarylation of tryptamines exemplified by the synthesis of 2-pyrazolyltryptamines”, Mendeleev Commun., 33:5 (2023), 645–647 |
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| 4. |
A. A. Zubenko, A. S. Morkovnik, L. N. Divaeva, V. S. Sochnev, O. P. Demidov, L. N. Fetisov, N. O. Andros, A. E. Svyatogorova, A. I. Klimenko, “New β-[<i>o</i>-(5-oxopyrazol-3-yl)aryl]ethylamines and their unusual metastable betaine form”, Mendeleev Commun., 33:2 (2023), 203–205 |
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| 5. |
M. P. Vlasenko, A. F. Pozharskii, O. P. Demidov, V. A. Ozeryanskii, G. S. Borodkin, “α-Amino acid-assisted autoxidation of naphthalene proton sponge affording 1,4-naphthoquinone nitrogen derivatives”, Mendeleev Commun., 33:2 (2023), 197–200 |
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2022 |
| 6. |
V. S. Sochnev, A. S. Morkovnik, A. A. Zubenko, L. N. Divaeva, O. P. Demidov, T. N. Gribanova, L. N. Fetisov, V. V. Chekrysheva, K. N. Kononenko, M. A. Bodryakova, A. I. Klimenko, G. S. Borodkin, I. A. Estrin, “Novel recyclization of 3,4-dihydroisoquinolines as an efficient route to a new type of heteroarylated derivatives of β-arylethylamines”, Mendeleev Commun., 32:6 (2022), 795–797 |
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| 7. |
I. O. Tupaeva, O. P. Demidov, E. V. Vetrova, E. A. Gusakov, T. A. Krasnikova, L. D. Popov, A. A. Zubenko, L. N. Fetisov, Yu. A. Sayapin, A. V. Metelitsa, V. I. Minkin, “Synthesis, molecular structure and biological activity of Ni<sup>ii</sup> complexes based on substituted 2-(2-hydroxyphenyl)benzoxazole”, Mendeleev Commun., 32:6 (2022), 763–765 |
| 8. |
A. V. Chernyshev, E. V. Solov'eva, I. A. Rostovtseva, N. A. Voloshin, O. P. Demidov, K. E. Shepelenko, A. V. Metelitsa, “Photo- and ionochromic properties of new spirobenzochromene-pyranoquinoline”, Mendeleev Commun., 32:4 (2022), 531–533 |
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| 9. |
A. A. Kolodina, D. V. Steglenko, E. S. Khodykina, N. I. Gaponenko, M. S. Galkina, O. P. Demidov, A. V. Metelitsa, “Unusual cyclization of <i>N</i>-imidazolyl quinone imines with the formation of thiadiazole ring and its subsequent recyclization”, Mendeleev Commun., 32:3 (2022), 386–389 |
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| 10. |
A. A. Zubenko, A. S. Morkovnik, L. N. Divaeva, V. S. Sochnev, O. P. Demidov, A. I. Klimenko, L. N. Fetisov, A. N. Bodryakov, M. A. Bodryakova, G. S. Borodkin, “New type of recyclization in 3,4-dihydroisoquinolines in the synthesis of β-(o-indazolylaryl)ethylamines and their 7-azaindazolyl analogues”, Mendeleev Commun., 32:2 (2022), 265–267 |
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2021 |
| 11. |
A. A. Zubenko, V. S. Sochnev, V. G. Kartsev, L. N. Divaeva, O. P. Demidov, A. I. Klimenko, A. N. Bodryakov, M. A. Bodryakova, G. S. Borodkin, A. S. Morkovnik, “Systems with annulated thioxo azepinone moiety: an access through heterocyclic carbodithioate ring expansion”, Mendeleev Commun., 31:4 (2021), 545–547 |
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| 12. |
A. A. Zubenko, A. S. Morkovnik, L. N. Divaeva, O. P. Demidov, V. G. Kartsev, V. S. Sochnev, A. I. Klimenko, N. M. Dobaeva, G. S. Borodkin, A. N. Bodryakov, M. A. Bodryakova, L. N. Fetisov, “Thiourea assisted recyclization of 1-(chloromethyl)dihydroisoquinolines: a convenient route to β-(<i>o</i>-thiazolylaryl)ethylamines”, Mendeleev Commun., 31:1 (2021), 125–127 |
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2020 |
| 13. |
A. A. Zubenko, A. S. Morkovnik, L. N. Divaeva, O. P. Demidov, V. S. Sochnev, I. G. Borodkina, Yu. D. Drobin, A. A. Spasov, “New route to bioactive 2-(hetero)arylethylamines <i>via</i> nucleophilic ring opening in fused 7-acyl-2,3-dihydroazepines”, Mendeleev Commun., 30:1 (2020), 28–30 |
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