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Publications in Math-Net.Ru |
Citations |
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2021 |
| 1. |
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   |
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2019 |
| 2. |
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 |
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2018 |
| 3. |
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 |
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2015 |
| 4. |
M. A. Epishina, A. S. Kulikov, N. V. Ignat'ev, M. Schulte, N. N. Makhova, “Efficient synthesis of tertiary acyclic amides by the Chapman rearrangement of aryl benzimidates in ionic liquids”, Mendeleev Commun., 25:2 (2015), 126–128 |
7
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| 5. |
M. A. Epishina, A. S. Kulikov, N. V. Ignat'ev, M. Schulte, N. N. Makhova, “Nucleophilic aromatic <i>cine</i>-substitution of hydrogen: the ionic liquid-promoted von Richter reaction”, Mendeleev Commun., 25:1 (2015), 41–43 |
9
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| 6. |
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 |
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2013 |
| 7. |
M. I. Pleshchev, M. A. Epishina, V. V. Kachala, V. V. Kuznetsov, A. S. Goloveshkin, I. S. Bushmarinov, N. N. Makhova, “Ionic liquid-promoted stereoselective [3 + 2] cycloaddition of 1-hetaryl-2-nitroethenes to azomethine imines generated in situ”, Mendeleev Commun., 23:4 (2013), 206–208 |
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2012 |
| 8. |
M. A. Epishina, A. S. Kulikov, M. I. Struchkova, N. V. Ignat'ev, M. Schulte, N. N. Makhova, “Ionic Liquids-assisted Synthesis of 3,4-Dihydroisoquinolines by the Bishler–Napieralski Reaction”, Mendeleev Commun., 22:5 (2012), 267–269 |
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2011 |
| 9. |
M. A. Epishina, A. S. Kulikov, N. V. Ignat'ev, M. Schulte, N. N. Makhova, “Ionic liquid-assisted synthesis of 5-monoand 1,5-disubstituted tetrazoles”, Mendeleev Commun., 21:6 (2011), 334–336 |
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| 10. |
M. A. Epishina, A. S. Kulikov, N. V. Ignat'ev, M. Schulte, N. N. Makhova, “Synthesis of 5-alkyl-2-amino-1,3,4-thiadiazoles and α,ω-bis(2-amino-1,3,4-thiadiazol-5-yl)alkanes in ionic liquids”, Mendeleev Commun., 21:6 (2011), 331–333 |
22
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| 11. |
M. A. Epishina, I. V. Ovchinnikov, A. S. Kulikov, N. N. Makhova, V. A. Tartakovsky, “Henry and Mannich reactions of polynitroalkanes in ionic liquids”, Mendeleev Commun., 21:1 (2011), 21–23 |
27
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2010 |
| 12. |
M. A. Epishina, A. S. Kulikov, N. V. Ignat'ev, M. Schulte, N. N. Makhova, “The first example of the Schmidt reaction in ionic liquids”, Mendeleev Commun., 20:6 (2010), 335–336 |
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2009 |
| 13. |
I. V. Ovchinnikov, A. O. Finogenov, M. A. Epishina, Yu. A. Strelenko, N. N. Makhova, “Synthesis of 1,3- and 1,4-bis(3-nitrofurazan-4-yl)benzenes and isomeric 1,3- and 1,4-bis[3(4)-nitrofuroxan-4(3)-yl]benzenes”, Mendeleev Commun., 19:4 (2009), 217–219 |
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2008 |
| 14. |
Yu. S. Syroeshkina, V. V. Kuznetsov, M. I. Struchkova, M. A. Epishina, N. N. Makhova, “Diaziridine ring expansion in 6-aryl-1,5-diazabicyclo[3.1.0]hexanes on treatment with nitriles assisted by ionic liquids”, Mendeleev Commun., 18:4 (2008), 207–208 |
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2006 |
| 15. |
S. I. Molotov, M. A. Epishina, A. S. Kulikov, Yu. V. Nelyubina, K. A. Lyssenko, K. Yu. Suponitsky, N. N. Makhova, “Thermally induced rearrangement of the arylhydrazones of furoxan-3-yl carbonyl compounds”, Mendeleev Commun., 16:5 (2006), 259–262 |
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2003 |
| 16. |
I. V. Ovchinnikov, M. A. Epishina, S. I. Molotov, Yu. A. Strelenko, K. A. Lyssenko, N. N. Makhova, “New rearrangement of azofuroxans in an oxidising medium”, Mendeleev Commun., 13:6 (2003), 272–275 |
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1994 |
| 17. |
M. A. Epishina, N. N. Makhova, L. V. Batog, L. S. Konstantinova, L. I. Khmel'nitskii, “New Macrocyclic Systems – Tetrafurazano[3,4-<i>c</i>:3,4-<i>e</i>:3,4-<i>i</i>:3,4-<i>k</i>]-1,2,7,8-tetraazacyclododeca-1,3,5,7,9,11-hexane and Hexafurazano-[3,4-<i>c</i>:3,4-<i>e</i>:3,4-<i>i</i>:3,4-<i>k</i>:3,4-<i>o</i>:3,4-<i>r</i>]-1,2,7,8,13,14-hexaazacyclooctadeca-1,3,5,7,9,11,13,15,17-nonane by Oxidative Macrocyclization of Diaminodifurazanyl”, Mendeleev Commun., 4:3 (1994), 102 |
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