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Публикации в базе данных Math-Net.Ru |
Цитирования |
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2024 |
| 1. |
O. V. Turova, A. A. Nigmatov, E. V. Filatova, A. A. Vasil'ev, S. G. Zlotin, “Organocatalytic domino formation of (3R,3aS,9bR )-configured 3-aryl-3a-benzamido-1,3a,4,9b-tetrahydrochromeno[4,3b]pyrroles in carbon dioxide medium”, Mendeleev Commun., 34:5 (2024), 694–697  |
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2023 |
| 2. |
A. V. Budkova, V. G. Merkulov, R. E. Ivanov, M. N. Zharkov, I. V. Kuchurov, S. G. Zlotin, “Application of NO2/supercritical CO2 system for safe and selective nitration of adamantanes and tertiary alkyl bromides”, Mendeleev Commun., 33:4 (2023), 461–462 |
5
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| 3. |
С. Г. Злотин, К. С. Егорова, В. П. Анаников, А. А. Акулов, М. В. Вараксин, О. Н. Чупахин, В. Н. Чарушин, К. П. Брыляков, А. Д. Аверин, И. П. Белецкая, Е. Л. Доленговский, Ю. Г. Будникова, О. Г. Синяшин, З. Н. Гафуров, А. О. Кантюков, Д. Г. Яхваров, А. В. Аксенов, М. Н. Элинсон, В. Г. Ненайденко, А. М. Чибиряев, Н. С. Нестеров, Е. А. Козлова, О. Н. Мартьянов, И. А. Балова, В. Н. Сорокоумов, Д. А. Гук, Е. К. Белоглазкина, Д. А. Леменовский, И. Ю. Чукичева, Л. Л. Фролова, Е. С. Изместьев, И. А. Дворникова, А. В. Попов, А. В. Кучин, Д. М. Борисова, А. А. Калинина, А. М. Музафаров, И. В. Кучуров, А. Л. Максимов, А. В. Золотухина, “Парадигма зеленой химии в современном органическом синтезе”, Усп. хим., 92:12 (2023), RCR5104 ; S. G. Zlotin, K. S. Egorova, V. P. Ananikov, A. A. Akulov, M. V. Varaksin, O. N. Chupakhin, V. N. Charushin, K. P. Bryliakov, A. D. Averin, I. P. Beletskaya, E. L. Dolengovski, Yu. H. Budnikova, O. G. Sinyashin, Z. N. Gafurov, A. O. Kantyukov, D. G. Yakhvarov, A. V. Aksenov, M. N. Elinson, V. G. Nenajdenko, A. M. Chibiryaev, N. S. Nesterov, E. A. Kozlova, O. N. Mart'yanov, I. A. Balova, V. N. Sorokoumov, D. A. Guk, E. K. Beloglazkina, D. A. Lemenovskii, I. Yu. Chukicheva, L. L. Frolova, E. S. Izmest'ev, I. A. Dvornikova, A. V. Popov, A. V. Kutchin, D. M. Borisova, A. A. Kalinina, A. M. Muzafarov, I. V. Kuchurov, A. L. Maksimov, A. V. Zolotukhina, “The green chemistry paradigm in modern organic synthesis”, Russian Chem. Reviews, 92:12 (2023), RCR5104   |
27
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2021 |
| 4. |
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 |
85
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| 5. |
A. A. Vasil'ev, A. S. Burukin, G. M. Zhdankina, S. G. Zlotin, “Buchwald ligand-assisted Suzuki cross-coupling of polychlorobenzenes”, Mendeleev Commun., 31:3 (2021), 400–402 |
7
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2020 |
| 6. |
S. G. Zlotin, O. A. Banina, D. V. Sudarikov, A. A. Nigmatov, L. L. Frolova, A. V. Kutchin, “Asymmetric aldol reaction of isatins with acetone in the presence of terpene amino alcohols”, Mendeleev Commun., 30:2 (2020), 147–149 |
7
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| 7. |
Е. С. Алексеев, А. Ю. Алентьев, А. С. Белова, В. И. Богдан, Т. В. Богдан, А. В. Быстрова, Э. Р. Гафарова, Е. Н. Голубева, Е. А. Гребеник, О. И. Громов, В. А. Даванков, С. Г. Злотин, М. Г. Киселев, А. Е. Коклин, Ю. Н. Кононевич, А. Э. Лажко, В. В. Лунин, С. Е. Любимов, О. Н. Мартьянов, И. И. Мишанин, А. М. Музафаров, Н. С. Нестеров, А. Ю. Николаев, Р. Д. Опарин, О. О. Паренаго, О. П. Паренаго, Я. А. Покусаева, И. А. Ронова, А. Б. Соловьева, М. Н. Темников, П. С. Тимашев, О. В. Турова, Е. В. Филатова, А. А. Филиппов, А. М. Чибиряев, А. С. Шалыгин, “Сверхкритические флюиды в химии”, Усп. хим., 89:12 (2020), 1337–1427  ; E. S. Alekseev, A. Yu. Alentiev, A. S. Belova, V. I. Bogdan, T. V. Bogdan, A. V. Bystrova, E. R. Gafarova, E. N. Golubeva, E. A. Grebenik, O. I. Gromov, V. A. Davankov, S. G. Zlotin, M. G. Kiselev, A. E. Koklin, Yu. N. Kononevich, A. E. Lazhko, V. V. Lunin, S. E. Lyubimov, O. N. Mart'yanov, I. I. Mishanin, A. M. Muzafarov, N. S. Nesterov, A. Yu. Nikolaev, R. D. Oparin, O. O. Parenago, O. P. Parenago, Ya. A. Pokusaeva, I. A. Ronova, A. B. Solovieva, M. N. Temnikov, P. S. Timashev, O. V. Turova, E. V. Filatova, A. A. Philippov, A. M. Chibiryaev, A. S. Shalygin, “Supercritical fluids in chemistry”, Russian Chem. Reviews, 89:12 (2020), 1337–1427 |
80
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| 8. |
С. Г. Злотин, И. Л. Далингер, Н. Н. Махова, В. А. Тартаковский, “Нитросоединения — структурная основа перспективных энергоемких материалов и многоцелевые реагенты для органического синтеза”, Усп. хим., 89:1 (2020), 1–54 ; S. G. Zlotin, I. L. Dalinger, N. N. Makhova, V. A. Tartakovsky, “Nitro compounds as the core structures of promising energetic materials and versatile reagents for organic synthesis”, Russian Chem. Reviews, 89:1 (2020), 1–54 |
82
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2017 |
| 9. |
S. G. Zlotin, A. M. Churakov, I. L. Dalinger, O. A. Luk'yanov, N. N. Makhova, A. Yu. Sukhorukov, V. A. Tartakovsky, “Recent advances in synthesis of organic nitrogen–oxygen systems for medicine and materials science”, Mendeleev Commun., 27:6 (2017), 535–546 |
46
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| 10. |
S. V. Kochetkov, A. S. Kucherenko, S. G. Zlotin, “Asymmetric Michael addition of aldehydes to maleimides in primary amine-based aqueous ionic liquid-supported recyclable catalytic system”, Mendeleev Commun., 27:5 (2017), 473–475 |
14
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| 11. |
N. A. Troitskaya-Markova, O. G. Vlasova, T. I. Godovikova, S. G. Zlotin, O. A. Rakitin, “Bis[1,2,5]oxadiazolo[3,4-c:3',4'-e]pyridazine 4,5-dioxide as a synthetic equivalent of 4,4'-dinitroso-3,3'-bifurazan”, Mendeleev Commun., 27:5 (2017), 448–450 |
7
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| 12. |
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 |
88
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| 13. |
М. Г. Виноградов, О. В. Турова, С. Г. Злотин, “Новые достижения в химии N-ацилиминиевых ионов и их использовании в стереоселективном органическом синтезе”, Усп. хим., 86:1 (2017), 1–17 ; M. G. Vinogradov, O. V. Turova, S. G. Zlotin, “The progress in the chemistry of N-acyliminium ions and their use in stereoselective organic synthesis”, Russian Chem. Reviews, 86:1 (2017), 1–17 |
25
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2016 |
| 14. |
A. A. Sukhanova, Yu. V. Nelyubina, S. G. Zlotin, “Asymmetric synthesis of 3-prenyl-substituted pyrrolidin-2-ones”, Mendeleev Commun., 26:6 (2016), 471–473 |
11
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| 15. |
A. S. Kucherenko, V. V. Perepelkin, G. M. Zhdankina, G. V. Kryshtal', E. Srinivasan, H. Inani, S. G. Zlotin, “Ionic liquid supported 4-HO-Pro-Val derived organocatalysts for asymmetric aldol reactions in the presence of water”, Mendeleev Commun., 26:5 (2016), 388–390 |
17
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| 16. |
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 |
86
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2015 |
| 17. |
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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| 18. |
S. G. Zlotin, A. M. Churakov, O. A. Luk'yanov, N. N. Makhova, A. Yu. Sukhorukov, V. A. Tartakovsky, “Novel approaches to pharmacology-oriented and energy rich organic nitrogen–oxygen systems”, Mendeleev Commun., 25:6 (2015), 399–409 |
65
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| 19. |
L. S. Konstantinova, S. A. Amelichev, S. G. Zlotin, M. I. Struchkova, T. I. Godovikova, O. A. Rakitin, “[1,4]Dithiino[2,3-c:5,6-c']bis[1,2,5]oxadiazole di-N-oxide: synthesis and oxidation to mono- and bis-S-oxides”, Mendeleev Commun., 25:5 (2015), 339–340 |
14
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| 20. |
S. V. Kochetkov, A. S. Kucherenko, S. G. Zlotin, “Asymmetric aldol reactions in ketone/ketone systems catalyzed by ionic liquid-supported C<sub>2</sub>-symmetrical organocatalyst”, Mendeleev Commun., 25:3 (2015), 168–170 |
20
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| 21. |
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 |
170
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| 22. |
M. N. Zharkov, I. V. Kuchurov, I. V. Fomenkov, S. G. Zlotin, V. A. Tartakovsky, “Nitration of glycoluril derivatives in liquid carbon dioxide”, Mendeleev Commun., 25:1 (2015), 15–16 |
17
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| 23. |
С. Г. Злотин, С. В. Кочетков, “$C_2$-симмeтpичныe диaмины и иx пpoизвoдныe – пepcпeктивныe opгaнoкaтaлизaтopы для acиммeтpичecкoгo cинтeзa”, Усп. хим., 84:11 (2015), 1077–1099 ; S. G. Zlotin, S. V. Kochetkov, “$C_2$-symmetric diamines and their derivatives as promising organocatalysts for asymmetric synthesis”, Russian Chem. Reviews, 84:11 (2015), 1077–1099 |
36
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2014 |
| 24. |
Zh. A. Krasnaya, V. V. Kachala, S. G. Zlotin, “Synthesis and conformations of cross-conjugated polyenes containing heterocyclic moieties with diverse structures”, Mendeleev Commun., 24:6 (2014), 377–379 |
6
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| 25. |
S. G. Zlotin, G. V. Kryshtal', G. M. Zhdankina, A. A. Sukhanova, A. S. Kucherenko, B. B. Smirnov, V. A. Tartakovsky, “Kinetic resolution of racemic (cyclohexyl)(geranyl)acetic acid”, Mendeleev Commun., 24:5 (2014), 257–259 |
4
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| 26. |
A. O. Chizhov, N. N. Makhova, I. V. Kuchurov, A. B. Sheremetev, S. G. Zlotin, “Unusual behavior of benzofuroxans under ESI MS conditions in negative ion mode”, Mendeleev Commun., 24:3 (2014), 165–166 |
6
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| 27. |
D. V. Khakimov, I. V. Kuchurov, I. V. Fomenkov, T. S. Pivina, S. G. Zlotin, V. A. Tartakovsky, “Simulation of ozone and molecular oxygen oxidation of dinitrogen tetroxide to nitric anhydride”, Mendeleev Commun., 24:2 (2014), 94–95 |
| 28. |
A. A. Vasil'ev, S. G. Zlotin, “Palladium-catalyzed allylation of malonic acid derivatives in heterogeneous systems containing ionic liquids”, Mendeleev Commun., 24:1 (2014), 23–25 |
6
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2013 |
| 29. |
Zh. A. Krasnaya, V. A. Kuzmin, L. V. Litvinkova, E. O. Dorofeeva, S. G. Zlotin, “Synthesis of thiacyanine dyes containing coumarin moieties at benzothiazole rings”, Mendeleev Commun., 23:4 (2013), 212–214 |
2
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| 30. |
A. A. Vasil'ev, I. V. Kuchurov, S. G. Zlotin, “Tsuji−Trost allylation of CH acids in supercritical carbon dioxide: advantages and problems”, Mendeleev Commun., 23:2 (2013), 84–85 |
5
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| 31. |
I. V. Kuchurov, I. V. Fomenkov, S. G. Zlotin, V. A. Tartakovsky, “Nitration of carbonic, sulfuric and oxalic
acid-derived amides in liquid carbon dioxide”, Mendeleev Commun., 23:2 (2013), 81–83 |
9
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| 32. |
G. V. Kryshtal', G. M. Zhdankina, S. G. Zlotin, “KOH-promoted synthesis of oxirane functional derivatives from diethyl bromomalonate and aldehydes under phase-transfer catalysis conditions”, Mendeleev Commun., 23:1 (2013), 24–25 |
3
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2012 |
| 33. |
N. I. Simirskaya, N. V. Ignat'ev, M. Schulte, S. G. Zlotin, “Mannich synthesis of acetylenic amino alcohols in aqueous ionic liquids”, Mendeleev Commun., 22:6 (2012), 317–319 |
8
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| 34. |
O. V. Turova, I. V. Kuchurov, E. V. Starodubtseva, V. A. Ferapontov, N. S. Ikonnikov, S. G. Zlotin, M. G. Vinogradov, “Ru–BINAP-catalyzed asymmetric hydrogenation of keto esters in high pressure carbon dioxide”, Mendeleev Commun., 22:4 (2012), 184–186 |
7
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| 35. |
I. V. Kuchurov, I. V. Fomenkov, S. G. Zlotin, V. A. Tartakovsky, “Synthesis of nitric acid esters from alcohols in a dinitrogen pentoxide/carbon dioxide liquid system”, Mendeleev Commun., 22:2 (2012), 67–69 |
11
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| 36. |
A. A. Vasil'ev, S. E. Lyubimov, E. P. Serebryakov, V. A. Davankov, S. G. Zlotin, “Asymmetric Tsuji–Trost substitution in 3-acetoxy-1,3-diphenylpropene under phase-transfer conditions”, Mendeleev Commun., 22:1 (2012), 39–40 |
7
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2011 |
| 37. |
O. V. Maltsev, A. S. Kucherenko, S. G. Zlotin, “Ionic polymer-supported O-trimethylsilyl-α,α-diphenyl-(S)-prolinols as recoverable organocatalysts for the asymmetric Michael reactions of carbon acids with α,β-enals”, Mendeleev Commun., 21:3 (2011), 146–148 |
18
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| 38. |
N. I. Simirskaya, N. V. Ignat'ev, M. Schulte, S. G. Zlotin, “Unprecedented acceleration of the domino reaction between methyl 4-hydroxyalk-3-ynoates and amines in ionic liquids”, Mendeleev Commun., 21:2 (2011), 94–96 |
6
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| 39. |
О. В. Мальцев, И. П. Белецкая, С. Г. Злотин, “Органокаталитические реакции Михаэля и Фриделя–Крафтса в энантиоселективном синтезе биологически активных веществ”, Усп. хим., 80:11 (2011), 1119–1165 ; O. V. Maltsev, I. P. Beletskaya, S. G. Zlotin, “Organocatalytic Michael and Friedel–Crafts reactions in enantioselective synthesis of biologically active compounds”, Russian Chem. Reviews, 80:11 (2011), 1067–1113 |
60
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2010 |
| 40. |
S. E. Lyubimov, I. V. Kuchurov, A. A. Vasil'ev, S. G. Zlotin, V. A. Davankov, “Asymmetric allylic alkylation in supercritical carbon dioxide using P*-chiral diamidophosphite ligands”, Mendeleev Commun., 20:3 (2010), 143–144 |
11
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| 41. |
I. V. Kuchurov, A. A. Vasil'ev, S. G. Zlotin, “The Suzuki–Miyaura cross-coupling of bromo- and chloroarenes with arylboronic acids in supercritical carbon dioxide”, Mendeleev Commun., 20:3 (2010), 140–142 |
21
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| 42. |
S. G. Zlotin, N. N. Makhova, “Ionic liquids as substrate-specific recoverable solvents and catalysts of regio-, stereo- and enantioselective organic reactions”, Mendeleev Commun., 20:2 (2010), 63–71 |
38
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| 43. |
С. Г. Злотин, Н. Н. Махова, “Реакции CH-кислот и 1,3-диполей в присутствии ионных жидкостей”, Усп. хим., 79:7 (2010), 603–644 ; S. G. Zlotin, N. N. Makhova, “Reactions of carbon acids and 1,3-dipoles in the presence of ionic liquids”, Russian Chem. Reviews, 79:7 (2010), 543–583 |
40
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2009 |
| 44. |
A. A. Vasil'ev, S. E. Lyubimov, E. P. Serebryakov, V. A. Davankov, S. G. Zlotin, “Regioselective palladium-catalysed prenylation of CH acids in the presence of diamidophosphite ligands and potassium carbonate”, Mendeleev Commun., 19:2 (2009), 103–105 |
9
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| 45. |
С. Г. Злотин, А. С. Кучеренко, И. П. Белецкая, “Органический катализ асимметрической альдольной реакции. Катализаторы и реагенты”, Усп. хим., 78:8 (2009), 796–845 ; S. G. Zlotin, A. S. Kucherenko, I. P. Beletskaya, “Organocatalysis of asymmetric aldol reaction. Catalysts and reagents”, Russian Chem. Reviews, 78:8 (2009), 737–784 |
126
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2007 |
| 46. |
Zh. A. Krasnaya, E. O. Tret'yakova, V. V. Kachala, S. G. Zlotin, “Synthesis of conjugated polynitriles by the reactions of β-dimethylaminoacrolein aminal and 1-dimethylamino-1,3,3-trimethoxypropane with 2-dicyanomethylene-4,5,5-trimethyl-3-cyano-2,5-dihydrofuran”, Mendeleev Commun., 17:6 (2007), 349–351 |
5
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| 47. |
A. S. Kucherenko, D. E. Siyutkin, V. O. Muraviev, M. I. Struchkova, S. G. Zlotin, “1(R),2(R)-Bis[(S)-prolinamido]cyclohexane/[bmim][BF<sub>4</sub>] ionic liquid as an efficient catalytic system for direct asymmetric aldol reactions”, Mendeleev Commun., 17:5 (2007), 277–278 |
14
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| 48. |
E. V. Starodubtseva, O. V. Turova, M. G. Vinogradov, V. A. Ferapontov, I. V. Razmanov, S. G. Zlotin, A. S. Kucherenko, “Asymmetric hydrogenation of the C=O bond with the recycling of an organometal catalyst deposited on a solid organic polyelectrolyte”, Mendeleev Commun., 17:1 (2007), 20–21 |
6
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| 49. |
А. А. Васильев, А. С. Бурукин, С. Г. Злотин, “Химическая функционализация полихлораренов”, Усп. хим., 76:10 (2007), 947–978 ; A. A. Vasil'ev, A. S. Burukin, S. G. Zlotin, “Chemical functionalisation of polychloroarenes”, Russian Chem. Reviews, 76:10 (2007), 885–916 |
12
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2006 |
| 50. |
Zh. A. Krasnaya, E. O. Tret'yakova, S. G. Zlotin, “Reactions of β-dimethylaminoacrolein aminal and 3-dimethylamino-1,1,3-tri-methoxypropane with alkylidenemalononitriles”, Mendeleev Commun., 16:6 (2006), 326–327 |
8
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2002 |
| 51. |
G. V. Kryshtal', G. M. Zhdankina, S. G. Zlotin, “Synthesis of α,β-unsaturated esters from dialkoxyphosphoryl esters and aldehydes in the ionic liquid [bmim][PF<sub>6</sub>]”, Mendeleev Commun., 12:5 (2002), 176–178 |
10
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| 52. |
G. V. Kryshtal', G. M. Zhdankina, S. G. Zlotin, “Alkylation of malonic and acetoacetic esters in an ionic liquid”, Mendeleev Commun., 12:2 (2002), 57–59 |
10
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1997 |
| 53. |
S. G. Zlotin, K. S. Chunikhin, M. O. Dekaprilevich, “Synthesis of 3,7-dichlorobisisothiazolo-[4,5-b:4',5'-e]-pyrazine: the first representative of a new heterocyclic system”, Mendeleev Commun., 7:3 (1997), 97 |
5
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| 54. |
S. G. Zlotin, E. A. Vinogradova, O. A. Luk'yanov, “Synthesis of 3,4:7,8:11,12-trifurazano-1,2,5,6,9,10-hexaazacyclododeca-1,3,5,7,9,11-hexaene-1,5,9-trioxide”, Mendeleev Commun., 7:1 (1997), 7–8 |
2
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1993 |
| 55. |
С. Г. Злотин, О. А. Лукьянов, “Региоселективные методы синтеза несимметрично замещенных диазеноксидов”, Усп. хим., 62:2 (1993), 157–183 ; S. G. Zlotin, O. A. Luk'yanov, “Regioselective methods of synthesis of asymmetrically substituted diazene oxides”, Russian Chem. Reviews, 62:2 (1993), 143–168 |
33
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1992 |
| 56. |
S. G. Zlotin, O. V. Prokshits, M. O. Dekaprilevich, O. A. Luk'yanov, “Synthesis of 3-Substituted 4-Imino-4,5-dihydro-1,2,3-triazole 1-Oxides and 4-Amino-1,2,3-triazole 1-Oxides”, Mendeleev Commun., 2:4 (1992), 131–134 |
6
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1991 |
| 57. |
S. G. Zlotin, M. Sharashkina, Yu. A. Strelenko, O. A. Luk'yanov, “A Regiospecific Synthesis of 1-Phosphonatodiazene-2-oxides”, Mendeleev Commun., 1:2 (1991), 49–50 |
7
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1989 |
| 58. |
С. Г. Злотин, Г. Н. Варнаева, О. А. Лукьянов, “α-Нитронитрилы”, Усп. хим., 58:5 (1989), 796–811 ; S. G. Zlotin, G. N. Varnaeva, O. A. Luk'yanov, “α-Nitronitriles”, Russian Chem. Reviews, 58:5 (1989), 470–478 |
12
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