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Publications in Math-Net.Ru |
Citations |
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2025 |
| 1. |
I. A. Stebletsova, A. A. Larin, L. L. Fershtat, “Recent advances in the synthesis of pharmacologically active 1,2,3-, 1,2,4-, and 1,2,5-oxadiazole-based lead compounds”, Usp. Khim., 94:10 (2025), 1–60 ; Russian Chem. Reviews, 94:10 (2025), 1–56 |
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2024 |
| 2. |
I. V. Ananyev, L. L. Fershtat, “Probing transferability of intermolecular interactions by their features: a nitro group case study”, Mendeleev Commun., 34:4 (2024), 540–542 |
| 3. |
V. N. Charushin, E. V. Verbitskiy, O. N. Chupakhin, D. V. Vorobyeva, P. S. Gribanov, S. N. Osipov, A. V. Ivanov, S. V. Martynovskaya, E. F. Sagitova, V. D. Dyachenko, I. V. Dyachenko, S. G. Krivokolylsko, V. V. Dotsenko, A. V. Aksenov, D. A. Aksenov, N. A. Aksenov, A. A. Larin, L. L. Fershtat, V. M. Muzalevskiy, V. G. Nenajdenko, A. V. Gulevskaya, A. F. Pozharskii, E. A. Filatova, K. V. Belyaeva, B. A. Trofimov, I. A. Balova, N. A. Danilkina, A. I. Govdi, A. S. Tikhomirov, A. E. Shchekotikhin, M. S. Novikov, N. V. Rostovskii, A. F. Khlebnikov, Yu. N. Klimochkin, M. V. Leonova, I. M. Tkachenko, V. A.-o. Mamedov, V. L. Mamedova, N. A. Zhukova, V. E. Semenov, O. G. Sinyashin, O. V. Borshchev, Yu. N. Luponosov, S. A. Ponomarenko, A. S. Fisyuk, A. S. Kostyuchenko, V. G. Ilkin, T. V. Beryozkina, V. A. Bakulev, A. S. Gazizov, A. A. Zagidullin, A. A. Karasik, M. E. Kukushkin, E. K. Beloglazkina, N. E. Golantsov, A. A. Festa, L. G. Voskresenskii, V. S. Moshkin, E. M. Buev, V. Ya. Sosnovskikh, I. A. Mironova, P. S. Postnikov, V. V. Zhdankin, M. S. Yusubov, I. A. Yaremenko, V. A. Vil', I. B. Krylov, A. O. Terent'ev, Yu. G. Gorbunova, A. G. Martynov, A. Yu. Tsivadze, P. A. Stuzhin, S. S. Ivanova, O. I. Koifman, O. N. Burov, M. E. Kletskii, S. V. Kurbatov, O. I. Yarovaya, K. P. Volcho, N. F. Salakhutdinov, M. A. Panova, Ya. V. Burgart, V. I. Saloutin, A. R. Sitdikova, E. S. Shchegravina, A. Yu. Fedorov, “The chemistry of heterocycles in the 21st century”, Usp. Khim., 93:7 (2024), 1–366 ; Russian Chem. Reviews, 93:7 (2024), 1–366 |
108
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| 4. |
A. V. Shaferov, L. L. Fershtat, “Energetic 1,2,4-oxadiazoles: synthesis and properties”, Usp. Khim., 93:2 (2024), 1–45 ; Russian Chem. Reviews, 93:2 (2024), 1–45 |
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2023 |
| 5. |
I. V. Ananyev, L. L. Fershtat, “Why pay more? QTAIM descriptors of non-covalent interactions in S22 from promolecular electron density”, Mendeleev Commun., 33:6 (2023), 806–808 |
4
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| 6. |
V. A. Sereda, L. L. Fershtat, “Divergent oriented synthesis of 2<i>H</i>-1,2,3-triazoles <i>via</i> rearrangement of furoxanylhydrazones”, Mendeleev Commun., 33:6 (2023), 764–766 |
3
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2022 |
| 7. |
A. A. Larin, L. L. Fershtat, “Energetic heterocyclic <i>N</i>-oxides: synthesis and performance”, Mendeleev Commun., 32:6 (2022), 703–713 |
36
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| 8. |
A. A. Larin, A. V. Shaferov, K. A. Monogarov, D. B. Meerov, A. N. Pivkina, L. L. Fershtat, “Novel energetic oxadiazole assemblies”, Mendeleev Commun., 32:1 (2022), 111–113 |
23
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2021 |
| 9. |
S. G. Zlotin, A. M. Churakov, M. P. Egorov, L. L. Fershtat, M. S. Klenov, I. V. Kuchurov, N. N. Makhova, G. A. Smirnov, Yu. V. Tomilov, V. A. Tartakovsky, “Advanced energetic materials: novel strategies and versatile applications”, Mendeleev Commun., 31:6 (2021), 731–749 |
96
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| 10. |
A. S. Kulikov, M. A. Epishina, E. S. Zhilin, A. D. Shuvaev, L. L. Fershtat, N. N. Makhova, “Design and synthesis of pyrazolo[3,4-<i>d</i>]pyridazine 5,6-dioxides as novel NO-donors”, Mendeleev Commun., 31:1 (2021), 42–45 |
18
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2020 |
| 11. |
N. N. Makhova, L. I. Belen'kii, G. A. Gazieva, I. L. Dalinger, L. S. Konstantinova, V. V. Kuznetsov, A. N. Kravchenko, M. M. Krayushkin, O. A. Rakitin, A. M. Starosotnikov, L. L. Fershtat, S. A. Shevelev, V. Z. Shirinian, V. N. Yarovenko, “Progress in the chemistry of nitrogen-, oxygen- and sulfur-containing heterocyclic systems”, Usp. Khim., 89:1 (2020), 55–124 ; Russian Chem. Reviews, 89:1 (2020), 55–124 |
146
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2019 |
| 12. |
M. A. Epishina, A. S. Kulikov, L. L. Fershtat, I. V. Ananyev, N. N. Makhova, “Synthesis of new pharmacologically oriented heterocyclic ensembles, [2-(1<i>H</i>-pyrazol-1-yl)thiazol-4-yl]furoxans”, Mendeleev Commun., 29:3 (2019), 288–291 |
8
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2018 |
| 13. |
A. S. Kulikov, M. A. Epishina, A. I. Churakov, L. V. Anikina, L. L. Fershtat, N. N. Makhova, “Regioselective synthesis, structural diversification and cytotoxic activity of (thiazol-4-yl)furoxans”, Mendeleev Commun., 28:6 (2018), 623–625 |
15
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| 14. |
A. A. Larin, L. L. Fershtat, N. E. Ustyuzhanina, M. L. Gening, N. E. Nifantiev, N. N. Makhova, “New hybrid furoxan structures with antiaggregant activity”, Mendeleev Commun., 28:6 (2018), 595–597 |
20
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| 15. |
B. V. Lyalin, V. L. Sigacheva, L. L. Fershtat, N. N. Makhova, V. A. Petrosyan, “Eco-friendly N–N coupling of aminofuroxans into azofuroxans under the action of electrogenerated hypohalites”, Mendeleev Commun., 28:5 (2018), 518–520 |
14
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| 16. |
N. E. Ustyuzhanina, L. L. Fershtat, M. L. Gening, N. E. Nifantiev, N. N. Makhova, “Antiaggregant activity of water-soluble furoxans”, Mendeleev Commun., 28:1 (2018), 49–51 |
30
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2016 |
| 17. |
N. E. Ustyuzhanina, L. L. Fershtat, M. L. Gening, N. E. Nifantiev, N. N. Makhova, “New insight into the antiaggregant activity of furoxans”, Mendeleev Commun., 26:6 (2016), 513–515 |
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| 18. |
L. L. Fershtat, N. N. Makhova, “Advances in the synthesis of non-annelated polynuclear heterocyclic systems comprising the 1,2,5-oxadiazole ring”, Usp. Khim., 85:10 (2016), 1097–1145 ; Russian Chem. Reviews, 85:10 (2016), 1097–1145 |
83
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2015 |
| 19. |
L. L. Fershtat, S. S. Ashirbaev, A. S. Kulikov, V. V. Kachala, N. N. Makhova, “Ionic liquid-mediated synthesis of (1<i>H</i>-1,2,3-triazol-1-yl)furoxans by [3 + 2] cycloaddition of azidofuroxans to acetylenes”, Mendeleev Commun., 25:4 (2015), 257–259 |
28
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| 20. |
L. L. Fershtat, M. A. Epishina, A. S. Kulikov, N. N. Makhova, “Design of hetarylthiofuroxans by nucleophilic substitution of NO<sub>2</sub> group in nitrofuroxans”, Mendeleev Commun., 25:1 (2015), 36–38 |
30
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2012 |
| 21. |
V. Yu. Petukhova, M. I. Pleshchev, L. L. Fershtat, V. V. Kuznetsov, V. V. Kachala, N. N. Makhova, “Metathesis of azomethine imines in the reaction of 6-aryl-1,5-diazabicyclo[3.1.0]hexanes with carbonyl compounds”, Mendeleev Commun., 22:1 (2012), 32–34 |
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