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Публикации в базе данных Math-Net.Ru |
Цитирования |
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2026 |
| 1. |
M. N. Elinson, Yu. E. Ryzhkova, V. M. Kalashnikova, M. P. Egorov, “Assembly of aldehydes and dimethylbarbituric acid into spirotricyclic furopyrimidines under the action of <em>N</em>-bromosuccinimide in water”, Mendeleev Commun., 36:1 (2026), 58–60  |
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2025 |
| 2. |
M. N. Elinson, Yu. E. Ryzhkova, V. M. Kalashnikova, M. P. Egorov, “Green multicomponent efficient approach to (aryl)di(hetaryl)methanes bearing barbituric and hydroxypyridone moieties”, Mendeleev Commun., 35:5 (2025), 515–517  |
| 3. |
M. V. Zabalov, B. N. Mankaev, M. P. Egorov, S. S. Karlov, “Random polymer formation in copolymerization of ʟ-lactide and ε-caprolactone initiated by aluminum pyridine-bis(phenolate): a quantum chemical study”, Mendeleev Commun., 35:4 (2025), 399–403  |
1
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| 4. |
M. N. Elinson, A. N. Vereshchagin, Yu. E. Ryzhkova, K. A. Karpenko, V. M. Kalashnikova, M. P. Egorov, “Tandem Knoevenagel–Michael reaction with oxidative cyclization in the synthesis of spiro[furo[3,2-<em>c</em>]pyran-2,5′ -pyrimidine] scaffold”, Mendeleev Commun., 35:3 (2025), 255–257 |
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2024 |
| 5. |
M. N. Elinson, Yu. E. Ryzhkova, V. M. Kalashnikova, A. O. Chizhov, A. N. Fakhrutdinov, M. P. Egorov, “First example of isatin used in four-component synthesis of ionic unsymmetrical scaffold with three different heterocyclic rings”, Mendeleev Commun., 34:6 (2024), 865–867 |
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2023 |
| 6. |
A. V. Lalov, A. Ya. Akyeva, M. P. Egorov, M. A. Syroeshkin, “Trends in ionization energies for group 14 catenates and influence of substituent nature on them”, Mendeleev Commun., 33:6 (2023), 746–749 |
| 7. |
E. N. Nikolaevskaya, M. A. Syroeshkin, M. P. Egorov, “Organic derivatives of group 14 elements: General aspects of synthesis, modern trends, and application prospects”, Mendeleev Commun., 33:6 (2023), 733–745 |
10
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| 8. |
M. N. Elinson, A. N. Vereshchagin, Yu. E. Ryzhkova, K. A. Karpenko, V. M. Kalashnikova, M. P. Egorov, “An expedient cyclization of polyfunctional (aryl)(pyrimidinyl)(pyranyl)methanes into spiro[furo[3,2-c]pyran-2,5'-pyrimidine] scaffold”, Mendeleev Commun., 33:4 (2023), 448–450 |
4
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| 9. |
M. U. Agaeva, B. N. Mankaev, V. I. Filippenko, V. A. Serova, M. P. Egorov, S. S. Karlov, “A convenient synthesis of N,N',N"-trisubstituted diethylenetriamines”, Mendeleev Commun., 33:2 (2023), 157–159 |
3
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| 10. |
М. Н. Темников, И. Н. Крижановский, А. А. Анисимов, С. П. Беденко, К. И. Дементьев, И. В. Крылова, С. А. Миленин, А. Л. Максимов, М. П. Егоров, А. М. Музафаров, “Прямой синтез алкоксисиланов: современное состояние, проблемы и перспективы”, Усп. хим., 92:7 (2023), RCR5081 ; M. N. Temnikov, I. N. Krizhanovskiy, A. A. Anisimov, S. P. Bedenko, K. I. Dementiev, I. V. Krylova, S. A. Milenin, A. L. Maksimov, M. P. Egorov, A. M. Muzafarov, “Direct synthesis of alkoxysilanes: current state, challenges and prospects”, Russian Chem. Reviews, 92:7 (2023), RCR5081 |
7
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2022 |
| 11. |
A. V. Lalov, M. P. Egorov, R. R. Aysin, “Probing the aromaticity of bis(diazolo)pyrazine radical anions”, Mendeleev Commun., 32:6 (2022), 732–734 |
| 12. |
M. N. Elinson, Yu. E. Ryzhkova, V. M. Kalashnikova, M. P. Egorov, “Noncatalytic on water aldol reaction of isatins with cyclic 1,3-diketones at room temperature without the need for subsequent chromatography”, Mendeleev Commun., 32:4 (2022), 543–545 |
2
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| 13. |
M. V. Zabalov, B. N. Mankaev, M. P. Egorov, S. S. Karlov, “DFT study of the role of substituents in tin(II) bis(amidoethyl)amine complexes used for ε-caprolactone polymerization”, Mendeleev Commun., 32:4 (2022), 460–463 |
2
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| 14. |
V. M. Khodonov, A. S. Kudinova, V. A. Kokorekin, V. A. Petrosyan, M. P. Egorov, “Effective metal-free electrooxidative thiocyanation of anilines”, Mendeleev Commun., 32:1 (2022), 94–96 |
4
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| 15. |
A. V. Kansuzyan, S. D. Farafonova, E. A. Saverina, I. V. Krylova, V. A. Balycheva, A. Ya. Akyeva, A. G. Medvedev, E. N. Nikolaevskaya, M. P. Egorov, P. V. Prikhodchenko, M. A. Syroeshkin, “Highly soluble germanium dioxide as a new source of germanium for derivatization with organic compounds”, Mendeleev Commun., 32:1 (2022), 25–27 |
5
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2021 |
| 16. |
V. I. Ovcharenko, A. B. Sheremetev, K. V. Strizhenko, S. V. Fokin, G. V. Romanenko, A. S. Bogomyakov, V. A. Morozov, M. A. Syroeshkin, A. Ya. Kozmenkova, A. V. Lalov, M. P. Egorov, “Novel organic magnet derived from pyrazine-fused furazans”, Mendeleev Commun., 31:6 (2021), 784–788 |
20
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| 17. |
Yu. V. Tomilov, L. G. Menchikov, E. A. Shapiro, V. D. Gvozdev, K. N. Shavrin, N. V. Volchkov, M. B. Lipkind, M. P. Egorov, S. E. Boganov, V. N. Khabashesku, E. G. Baskir, “Carbenes, related intermediates, and small-sized cycles: contribution from Professor Nefedov's laboratory”, Mendeleev Commun., 31:6 (2021), 750–768 |
9
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| 18. |
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 |
99
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| 19. |
V. D. Gvozdev, K. N. Shavrin, M. P. Egorov, O. M. Nefedov, “Synthesis of vicinal (alkylamino)alkynylcyclopropanes from geminal alkynyl(chloro)cyclopropanes”, Mendeleev Commun., 31:5 (2021), 654–656 |
5
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| 20. |
A. N. Vereshchagin, N. A. Frolov, A. P. Minaeva, E. V. Detusheva, Ya. V. Derkach, M. P. Egorov, “Synthesis and biological evaluation of novel cyanuric acid-tethered tris-pyridinium derivatives”, Mendeleev Commun., 31:3 (2021), 368–369 |
13
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| 21. |
M. N. Elinson, A. N. Vereshchagin, Yu. E. Ryzhkova, M. P. Egorov, “Selective and efficient electrocatalytic way to spirobarbituric dihydrofurans”, Mendeleev Commun., 31:3 (2021), 347–349 |
4
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| 22. |
S. E. Boganov, V. M. Promyslov, P. G. Shangin, M. A. Syroeshkin, M. P. Egorov, “Interaction of SiCl<sub>2</sub> with CO<sub>2</sub> in Ar matrices”, Mendeleev Commun., 31:2 (2021), 149–153 |
5
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2020 |
| 23. |
A. N. Vereshchagin, N. A. Frolov, A. S. Pakina, K. A. Hansford, M. P. Egorov, “Synthesis and biological evaluation of novel bispyridinium salts containing naphthalene-2,7-diylbis(oxy) spacer”, Mendeleev Commun., 30:6 (2020), 703–705 |
9
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| 24. |
V. Romanovs, D. M. Vakhrusheva, I. V. Krylova, B. N. Mankaev, A. Ya. Kozmenkova, M. A. Syroeshkin, M. P. Egorov, V. Jouikov, “1,1′-Diphenyl-bis-germatrane with persistent radical cation”, Mendeleev Commun., 30:5 (2020), 567–568 |
5
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| 25. |
I. V. Krylova, E. A. Saverina, S. S. Rynin, A. V. Lalov, M. E. Minyaev, E. N. Nikolaevskaya, M. A. Syroeshkin, M. P. Egorov, “Synthesis, characterization and redox properties of Ar–C=N→Ge←N=C–Ar containing system”, Mendeleev Commun., 30:5 (2020), 563–566 |
11
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| 26. |
A. N. Vereshchagin, N. A. Frolov, V. Yu. Konyuhova, E. O. Dorofeeva, K. A. Hansford, M. P. Egorov, “Synthesis and biological evaluation of novel bis-quaternary ammonium compounds with p-terphenyl spacer”, Mendeleev Commun., 30:4 (2020), 424–426 |
19
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| 27. |
M. N. Elinson, A. N. Vereshchagin, Yu. E. Ryzhkova, S. K. Krymov, N. A. Leonova, A. S. Goloveshkin, M. P. Egorov, “Electrocatalytic one-pot multicomponent assembly of aldehydes, 2,4-dihydro-3H-pyrazol-3-ones and kojic acid”, Mendeleev Commun., 30:2 (2020), 223–225 |
7
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| 28. |
M. N. Elinson, A. N. Vereshchagin, Yu. E. Anisina, N. A. Leonova, M. P. Egorov, “On water noncatalytic tandem Knoevenagel–Michael reaction of aldehydes, N,N'-dimethylbarbituric acid and cyclohexane-1,3-diones”, Mendeleev Commun., 30:1 (2020), 15–17 |
18
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2019 |
| 29. |
M. N. Elinson, A. N. Vereshchagin, Yu. E. Anisina, S. K. Krymov, A. N. Fakhrutdinov, M. P. Egorov, “Multicomponent assembling of salicylaldehydes, kojic acid and malonic acid derivatives”, Mendeleev Commun., 29:5 (2019), 581–583 |
9
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| 30. |
A. N. Vereshchagin, N. A. Frolov, V. Yu. Konyuhova, K. A. Hansford, M. P. Egorov, “Synthesis and microbiological properties of novel bis-quaternary ammonium compounds based on 4,4′-oxydiphenol spacer”, Mendeleev Commun., 29:5 (2019), 523–525 |
26
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| 31. |
A. N. Vereshchagin, E. O. Dorofeeva, M. N. Elinson, V. A. Korolev, M. P. Egorov, “Pyridinium bromide as a new mediator for electrochemical transformations involving CH-acids”, Mendeleev Commun., 29:4 (2019), 391–392 |
3
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| 32. |
V. D. Gvozdev, K. N. Shavrin, E. G. Baskir, O. M. Nefedov, M. P. Egorov, “Alkylthio(4-methylpent-3-en-1-ynyl)carbenes: generation by the photolysis of 5-alkylthioethynyl-3,3-dimethyl-3H-pyrazoles and reactions with alkenes”, Mendeleev Commun., 29:2 (2019), 140–142 |
7
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2018 |
| 33. |
S. E. Boganov, V. M. Promyslov, S. S. Rynin, I. V. Krylova, M. P. Egorov, “Formation of 1,1-dichloro-2-vinyl-1-silacyclopropane by a photoinduced reaction between dichlorosilylene and 1,3-butadiene”, Mendeleev Commun., 28:6 (2018), 574–576 |
6
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| 34. |
A. N. Vereshchagin, K. A. Karpenko, M. N. Elinson, E. O. Dorofeeva, A. S. Goloveshkin, M. P. Egorov, “Pseudo six-component stereoselective synthesis of 2,4,6-triaryl-3,3,5,5-tetracyanopiperidines”, Mendeleev Commun., 28:4 (2018), 384–386 |
16
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| 35. |
M. N. Elinson, A. N. Vereshchagin, Yu. E. Anisina, A. S. Goloveshkin, I. E. Ushakov, M. P. Egorov, “PASE facile and efficient multicomponent approach to the new type of 5-C-substituted 2,4-diamino-5H-chromeno[2,3-b]pyridine scaffold”, Mendeleev Commun., 28:4 (2018), 372–374 |
16
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| 36. |
V. D. Gvozdev, K. N. Shavrin, M. P. Egorov, O. M. Nefedov, “New selective cyclizations of alk-4-ynals with primary amines and azoles:one-pot synthesis of 2-azolylpyrrolidines and 3-iminocyclopentenes”, Mendeleev Commun., 28:2 (2018), 123–125 |
2
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| 37. |
Г. А. Абакумов, А. В. Пискунов, В. К. Черкасов, И. Л. Федюшкин, В. П. Анаников, Д. Б. Еремин, Е. Г. Гордеев, И. П. Белецкая, А. Д. Аверин, М. Н. Бочкарев, А. А. Трифонов, У. М. Джемилев, В. А. Дьяконов, М. П. Егоров, А. Н. Верещагин, М. А. Сыроешкин, В. В. Жуйков, А. М. Музафаров, А. А. Анисимов, А. В. Арзуманян, Ю. Н. Кононевич, М. Н. Темников, О. Г. Синяшин, Ю. Г. Будникова, А. Р. Бурилов, А. А. Карасик, В. Ф. Миронов, П. А. Стороженко, Г. И. Щербакова, Б. А. Трофимов, С. В. Амосова, Н. К. Гусарова, В. А. Потапов, В. Б. Шур, В. В. Бурлаков, В. С. Богданов, М. В. Андреев, “Перспективные точки роста и вызовы элементоорганической химии”, Усп. хим., 87:5 (2018), 393–507 ; G. A. Abakumov, A. V. Piskunov, V. K. Cherkasov, I. L. Fedushkin, V. P. Ananikov, D. B. Eremin, E. G. Gordeev, I. P. Beletskaya, A. D. Averin, M. N. Bochkarev, A. A. Trifonov, U. M. Dzhemilev, V. A. D'yakonov, M. P. Egorov, A. N. Vereshchagin, M. A. Syroeshkin, V. V. Jouikov, A. M. Muzafarov, A. A. Anisimov, A. V. Arzumanyan, Yu. N. Kononevich, M. N. Temnikov, O. G. Sinyashin, Yu. H. Budnikova, A. R. Burilov, A. A. Karasik, V. F. Mironov, P. A. Storozhenko, G. I. Shcherbakova, B. A. Trofimov, S. V. Amosova, N. K. Gusarova, V. A. Potapov, V. B. Shur, V. V. Burlakov, V. S. Bogdanov, M. V. Andreev, “Organoelement chemistry: promising growth areas and challenges”, Russian Chem. Reviews, 87:5 (2018), 393–507 |
166
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2017 |
| 38. |
M. N. Elinson, F. V. Ryzhkov, A. N. Vereshchagin, A. D. Korshunov, R. A. Novikov, M. P. Egorov, “'On-solvent' new domino reaction of salicylaldehyde, malononitrile and 4-hydroxy-6-methylpyridin-2(1H)-one: fast and efficient approach to medicinally relevant 4-pyridinyl-2-amino-4H-chromene scaffold”, Mendeleev Commun., 27:6 (2017), 559–561 |
18
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| 39. |
V. P. Ananikov, D. B. Eremin, S. A. Yakukhnov, A. D. Dilman, V. V. Levin, M. P. Egorov, S. S. Karlov, L. M. Kustov, A. L. Tarasov, A. A. Greish, A. A. Shesterkina, A. M. Sakharov, Z. N. Nysenko, A. B. Sheremetev, A. Yu. Stakheev, I. S. Mashkovsky, A. Yu. Sukhorukov, S. L. Ioffe, A. O. Terent'ev, V. A. Vil', Yu. V. Tomilov, R. A. Novikov, S. G. Zlotin, A. S. Kucherenko, N. E. Ustyuzhanina, V. B. Krylov, Yu. E. Tsvetkov, M. L. Gening, N. E. Nifantiev, “Organic and hybrid systems: from science to practice”, Mendeleev Commun., 27:5 (2017), 425–438 |
89
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| 40. |
V. D. Gvozdev, K. N. Shavrin, E. G. Baskir, M. P. Egorov, O. M. Nefedov, “Selective one-pot synthesis of 11-arylmethylidene-11H-isoindolo-[2,1-a]benzimidazoles and 6-arylbenzimidazo[2,1-a]isoquinolines from o-alkynylbenzaldehydes and o-diaminobenzenes”, Mendeleev Commun., 27:3 (2017), 231–233 |
14
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2016 |
| 41. |
M. N. Elinson, F. V. Ryzhkov, A. N. Vereshchagin, T. A. Zaimovskaya, V. A. Korolev, M. P. Egorov, “Multicomponent assembling of isatins, malononitrile and 4-hydroxy-6-methylpyridin-2(1H)-ones: one-pot efficient approach to privileged spiro[indoline-3,4'-pyrano[3,2-c]pyridine]-2,5'(6'H)-dione scaffold”, Mendeleev Commun., 26:5 (2016), 399–401 |
20
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| 42. |
V. P. Ananikov, K. I. Galkin, M. P. Egorov, A. M. Sakharov, S. G. Zlotin, E. A. Redina, V. I. Isaeva, L. M. Kustov, M. L. Gening, N. E. Nifantiev, “Challenges in the development of organic and hybrid molecular systems”, Mendeleev Commun., 26:5 (2016), 365–374 |
87
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| 43. |
A. N. Vereshchagin, M. N. Elinson, A. D. Korshunov, M. P. Egorov, “Highly efficient one-pot cascade cyclization of 3-(5-hydroxy-3-methylpyrazol-4-yl)-3-arylpropionitriles into spirocyclopropyl pyrazolones”, Mendeleev Commun., 26:1 (2016), 19–20 |
4
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| 44. |
V. D. Gvozdev, K. N. Shavrin, M. P. Egorov, O. M. Nefedov, “Stereoselective one-pot synthesis of (1Z)- and (1E)-1-arylmethylidene-2,3-dihydro-1H-pyrrolo[1,2-a]benzimidazoles by cyclization of alk-4-ynals with o-diaminobenzene”, Mendeleev Commun., 26:1 (2016), 3–5 |
8
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2015 |
| 45. |
A. N. Vereshchagin, M. N. Elinson, Yu. E. Anisina, F. V. Ryzhkov, A. S. Goloveshkin, I. S. Bushmarinov, S. G. Zlotin, M. P. Egorov, “Pot, atom and step economic (PASE) synthesis of 5-isoxazolyl-5H-chromeno[2,3-b]pyridine scaffold”, Mendeleev Commun., 25:6 (2015), 424–426 |
51
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| 46. |
V. D. Gvozdev, K. N. Shavrin, M. P. Egorov, O. M. Nefedov, “One-pot synthesis of 1-arylmethylidene-1,2,3,3a-tetrahydro-5H-pyrrolo[1,2-a]-[3,1]benzoxazines and 1-arylmethylidene-1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]-quinazolines from 5-arylalk-4-ynals and o-aminobenzylic alcohol/amine”, Mendeleev Commun., 25:5 (2015), 329–331 |
7
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| 47. |
M. N. Elinson, F. V. Ryzhkov, T. A. Zaimovskaya, M. P. Egorov, “Non-catalytic solvent-free synthesis of 5,6,7,8-tetrahydro-4H-chromenes from aldehydes, dimedone and malononitrlie at ambient temperature”, Mendeleev Commun., 25:3 (2015), 185–187 |
13
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| 48. |
V. P. Ananikov, E. A. Khokhlova, M. P. Egorov, A. M. Sakharov, S. G. Zlotin, A. V. Kucherov, L. M. Kustov, M. L. Gening, N. E. Nifantiev, “Organic and hybrid molecular systems”, Mendeleev Commun., 25:2 (2015), 75–82 |
175
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| 49. |
M. N. Elinson, O. O. Sokolova, R. F. Nasybullin, T. A. Zaimovskaya, M. P. Egorov, “Efficient non-catalytic synthesis of substituted 2,3,4,9-tetrahydro-1H-xanthen-1-ones from salicylaldehydes and dimedone”, Mendeleev Commun., 25:1 (2015), 19–20 |
7
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2014 |
| 50. |
M. N. Elinson, F. V. Ryzhkov, R. F. Nasybullin, T. A. Zaimovskaya, M. P. Egorov, “Sodium acetate catalyzed multicomponent approach to medicinally privileged 2-amino-4H-chromene scaffold from salicylaldehydes, malononitrile and cyanoacetates”, Mendeleev Commun., 24:3 (2014), 170–172 |
15
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2002 |
| 51. |
I. S. Orlov, A. A. Moiseeva, K. P. Butin, L. R. Sita, M. P. Egorov, O. M. Nefedov, “Electrochemistry of 1,1,2,2,3,3-hexa(2,6-diethylphenyl)cyclotristannane. The first examples of electrochemical generation of a stannylene radical anion and a tristannane radical cation”, Mendeleev Commun., 12:4 (2002), 125–126 |
10
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| 52. |
I. S. Orlov, M. P. Egorov, O. M. Nefedov, A. A. Moiseeva, K. P. Butin, D. Ostendorf, M. Weidenbruch, “Electrochemistry of a cyclotrisilane and a cyclotrigermane. The first example of the electrochemical generation of a cyclotrisilane radical anion”, Mendeleev Commun., 12:3 (2002), 89–90 |
2
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2001 |
| 53. |
B. G. Kimel, V. V. Tumanov, M. P. Egorov, O. M. Nefedov, “The first phosphagermacyclopropane prepared via cycloaddition of dimethylgermylene to the C=P double bond of phosphaalkene”, Mendeleev Commun., 11:3 (2001), 85–86 |
5
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1998 |
| 54. |
V. A. Bagryansky, Yu. N. Molin, M. P. Egorov, O. M. Nefedov, “The first experimental detection, by OD ESR spectroscopy, of radical anions of siloles and germoles bearing hydrogen and chlorine substituents attached to the heteroatom”, Mendeleev Commun., 8:6 (1998), 236–237 |
7
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1997 |
| 55. |
V. A. Bagryansky, V. I. Borovkov, Yu. N. Molin, M. P. Egorov, O. M. Nefedov, “Quantum beats in the recombination of radical ion pairs caused by hyperfine interaction in radical anions”, Mendeleev Commun., 7:4 (1997), 132–133 |
7
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| 56. |
R. Becerra, S. E. Boganov, M. P. Egorov, O. M. Nefedov, R. Walsh, “Direct time-resolved study of the kinetics of the gas-phase reaction of germylene with triethylgermane: a negative activation energy for the Ge–H insertion process”, Mendeleev Commun., 7:3 (1997), 87–88 |
28
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1992 |
| 57. |
M. P. Egorov, A. M. Gal'minas, O. M. Nefedov, “A New Method of Generating Anionic σ-Complexes by the Reaction of 7-Silanorbornadiene with Alkali”, Mendeleev Commun., 2:3 (1992), 105–106 |
2
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1991 |
| 58. |
M. P. Egorov, M. B. Ezhova, S. P. Kolesnikov, O. M. Nefedov, M. B. Taraban, A. I. Kruppa, T. V. Leshina, “<sup>1</sup>H CIDNP Study of the Addition Reaction of Me<sub>2</sub>E (E = Si,Ge) to a Carbon≡Carbon Triple Bond”, Mendeleev Commun., 1:4 (1991), 143–145 |
15
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2020 |
| 59. |
В. М. Бузник, В. В. Воронов, С. В. Гарнов, М. П. Егоров, В. К. Иванов, М. В. Ковальчук, В. И. Конов, Г. Я. Красников, Е. Е. Ломонова, П. П. Пашинин, В. Б. Цветков, И. А. Щербаков, “Памяти Вячеслава Васильевича Осико”, УФН, 190:2 (2020), 223–224 ; V. M. Bouznik, V. V. Voronov, S. V. Garnov, M. P. Egorov, V. K. Ivanov, M. V. Kovalchuk, V. I. Konov, G. Ya. Krasnikov, E. E. Lomonova, P. P. Pashinin, V. B. Tsvetkov, I. A. Shcherbakov, “In memory of Vyacheslav Vasil'evich Osiko”, Phys. Usp., 63:2 (2020), 204–206 |
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2019 |
| 60. |
М. П. Егоров, “Волшебный мир фторорганических соединений”, Усп. хим., 88:5 (2019), I ; M. P. Egorov, “The magic world of organofluorine compounds”, Russian Chem. Reviews, 88:5 (2019), I |
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2018 |
| 61. |
М. П. Егоров, “Элементоорганическая химия — инструмент стратегии научно-технического развития”, Усп. хим., 87:5 (2018), I ; M. P. Egorov, “Organoelement chemistry: a strategic tool for science and technology development”, Russian Chem. Reviews, 87:5 (2018), I |
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2011 |
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М. П. Егоров, Б. Ф. Мясоедов, “Номер посвящен главному редактору журнала “Успехи химии” академику ОЛЕГУ МАТВЕЕВИЧУ НЕФЕДОВУ в связи с 80-летием”, Усп. хим., 80:11 (2011), 1057–1059  ; M. P. Egorov, B. F. Myasoedov, “The issue is dedicated to Editor-in-Chief of Russian Chemical Reviews Academician OLEG M NEFEDOV on the occasion of his 80th birthday”, Russian Chem. Reviews, 80:11 (2011), I |
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2009 |
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М. П. Егоров, “Институт органической химии им. Н. Д. Зелинского Российской академии наук”, Усп. хим., 78:8 (2009), 739–741 ; M. P. Egorov, “N D Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences”, Russian Chem. Reviews, 78:8 (2009), 679–681 |
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