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Публикации в базе данных Math-Net.Ru |
Цитирования |
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2022 |
| 1. |
С. Ф. Василевский, А. А. Степанов, “Методы синтеза, реакционная способность и прикладные аспекты ацетиленовых производных хинонов и продуктов”, Усп. хим., 91:1 (2022), RCR5020   ; S. F. Vasilevskii, A. A. Stepanov, “Acetylene derivatives of quinones and their transformation products: synthesis, reactivity and applied aspects”, Russian Chem. Reviews, 91:1 (2022), RCR5020   |
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2021 |
| 2. |
P. A. Volkov, N. K. Gusarova, K. O. Khrapova, A. A. Telezhkin, A. I. Albanov, S. F. Vasilevskii, B. A. Trofimov, “A mechanistic insight into the chemoselectivity of the reaction between 3-phenyl-2-propynenitrile, secondary phosphine oxides and pyridinoids”, Mendeleev Commun., 31:5 (2021), 670–672 |
8
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2015 |
| 3. |
S. F. Vasilevskii, M. P. Davydova, V. I. Mamatyuk, N. V. Pleshkova, D. S. Fadeev, I. V. Alabugin, “Reaction of α,β-alkynylketones with β-amino alcohols: pseudoephedrine- assisted cleavage of triple bond via formal internal redox process”, Mendeleev Commun., 25:5 (2015), 377–379 |
9
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2013 |
| 4. |
A. I. Govdi, S. F. Vasilevskii, N. V. Sokolova, I. V. Sorokina, T. G. Tolstikova, V. G. Nenajdenko, “Betulonic acid–peptide conjugates: synthesis and evaluation of anti-inflammatory activity”, Mendeleev Commun., 23:5 (2013), 260–261 |
21
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2012 |
| 5. |
D. S. Baranov, A. A. Ryabichev, V. I. Mamatyuk, Yu. V. Gatilov, V. G. Kartsev, S. F. Vasilevskii, “Synthesis of 2-amino-5,5-dialkyl-4-arylmethylidene-2-oxazolines from 2-alkyl-4-arylbut-3-yn-2-ols and guanidine”, Mendeleev Commun., 22:2 (2012), 114–116 |
6
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2009 |
| 6. |
D. S. Baranov, S. F. Vasilevskii, V. I. Mamatyuk, Yu. V. Gatilov, “Multichannel reaction of 1-(3'-hydroxy-3'-methylbutynyl)-9,10-anthraquinone with guanidine”, Mendeleev Commun., 19:6 (2009), 326–328 |
10
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2008 |
| 7. |
B. A. Trofimov, S. F. Vasilevskii, N. K. Gusarova, S. F. Malysheva, D. S. Baranov, V. I. Mamatyuk, Yu. V. Gatilov, “Complex of tris(Z-styryl)phosphine with PdCl<sub>2</sub> as a new catalyst for the Sonogashira reaction”, Mendeleev Commun., 18:6 (2008), 318–319 |
12
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2007 |
| 8. |
B. A. Trofimov, S. F. Malysheva, N. K. Gusarova, N. A. Belogorlova, S. F. Vasilevskii, V. B. Kobychev, B. G. Sukhov, I. A. Ushakov, “Free-radical addition of phosphine sulfides to aryl and hetaryl acetylenes: unprecedented stereoselectivity”, Mendeleev Commun., 17:3 (2007), 181–182 |
16
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1999 |
| 9. |
E. V. Tret'yakov, R. I. Samoilova, Yu. V. Ivanov, V. F. Plyusnin, S. V. Pashchenko, S. F. Vasilevskii, “Stable free imino and nitronyl nitroxyl radicals of the acetylene series: synthesis, electronic absorption spectra and magnetic resonance parameters”, Mendeleev Commun., 9:3 (1999), 92–95 |
12
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1998 |
| 10. |
S. F. Vasilevskii, E. V. Tretyakov, O. M. Usov, Yu. N. Molin, S. V. Fokin, Yu. G. Shwedenkov, V. N. Ikorskii, G. V. Romanenko, R. Z. Sagdeev, V. I. Ovcharenko, “A new family of stable 2-imidazoline nitroxides”, Mendeleev Commun., 8:6 (1998), 216–218 |
21
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| 11. |
S. V. Klyatskaya, E. V. Tretyakov, S. F. Vasilevskii, “Synthesis and reactions of ethynylbenzocrown ethers”, Mendeleev Commun., 8:5 (1998), 201–203 |
4
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| 12. |
T. A. Prikhod'ko, S. F. Vasilevskii, “Cross-coupling of copper arylacetylides with N-(o-iodoaryl)hydrazines as a new method of synthesising 2-substituted indoles”, Mendeleev Commun., 8:4 (1998), 149–150 |
5
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1996 |
| 13. |
E. V. Tretyakov, S. F. Vasilevskii, “A route to pyrazolylazopyrazolo[4,3-c]pyrazoles via l,5-dimethyl-3R-pyrazolyl-4-diazonium salts”, Mendeleev Commun., 6:5 (1996), 190–191 |
9
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| 14. |
S. F. Vasilevskii, T. A. Prikhod'ko, “Cyclocondensation of activated ortho-chloroarylacetylenes with hydrazine: a novel route to substituted indazoles”, Mendeleev Commun., 6:3 (1996), 98–99 |
8
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1995 |
| 15. |
E. V. Tret'yakov, S. F. Vasilevskii, “Nitrodeiodination of Polyiodopyrazoles: a Convenient Synthesis of 4-Nitroiodopyrazoles”, Mendeleev Commun., 5:6 (1995), 233–234 |
14
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1990 |
| 16. |
А. Г. Пройдаков, Г. А. Калабин, С. Ф. Василевский, “Параметры спектров ЯМР <sup>13</sup>С замещенных ацетилена: связь с электронным строением и реакционной способностью”, Усп. хим., 59:1 (1990), 39–65 ; A. G. Proidakov, G. A. Kalabin, S. F. Vasilevskii, “The parameters of the <sup>13</sup>C NMR spectra of substituted acetylenes: relation with electronic structure and reactivity”, Russian Chem. Reviews, 59:1 (1990), 23–38 |
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