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Публикации в базе данных Math-Net.Ru |
Цитирования |
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2025 |
| 1. |
A. S. Chechulina, E. A. Knyazeva, O. A. Rakitin, “Benzo[<em>c</em>][1,2,5]thiadiazole doubly fused with thieno[2',3':4,5]thieno[3,2-<em>b</em>]pyrroles as a key building block for non-fullerene acceptors of Y6 series”, Mendeleev Commun., 35:5 (2025), 503–511   |
| 2. |
P. A. Koutentis, А. Ю. Макаров, О. А. Ракитин, А. В. Зибарев, “Химия Херца и ее применения в науке о низкомолекулярных функциональных материалах: достижения, проблемы и перспективы”, Усп. хим., 94:1 (2025), RCR5146 ; P. A. Koutentis, A. Yu. Makarov, O. A. Rakitin, A. V. Zibarev, “Herz chemistry and its applications in small-molecule functional materials science: achievements, challenges, and prospects”, Russian Chem. Reviews, 94:1 (2025), RCR5146  |
1
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2023 |
| 3. |
A. A. Buravlev, A. Yu. Makarov, O. A. Rakitin, A. V. Zibarev, “Wolmershäuser radicals: Chemistry and materials science”, Mendeleev Commun., 33:4 (2023), 439–447 |
7
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| 4. |
E. O. Levina, E. V. Bartashevich, A. E. Batalov, O. A. Rakitin, V. G. Tsirelson, “How electron delocalization influences the electron-withdrawing properties of isomeric benzobischalcogenadiazoles”, Mendeleev Commun., 33:3 (2023), 372–375 |
3
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2022 |
| 5. |
V. M. Korshunov, T. N. Chmovzh, G. R. Chkhetiani, I. V. Taidakov, O. A. Rakitin, “New D–A–D luminophores of the [1,2,5]thiadiazolo[3,4-d]pyridazine series”, Mendeleev Commun., 32:3 (2022), 371–373 |
12
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2021 |
| 6. |
L. S. Konstantinova, O. A. Rakitin, “Chalcogen exchange in chalcogen–nitrogen π-heterocycles”, Mendeleev Commun., 31:4 (2021), 433–441 |
8
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2020 |
| 7. |
Н. Н. Махова, Л. И. Беленький, Г. А. Газиева, И. Л. Далингер, Л. С. Константинова, В. В. Кузнецов, А. Н. Кравченко, М. М. Краюшкин, О. А. Ракитин, А. М. Старосотников, Л. Л. Ферштат, С. А. Шевелев, В. З. Ширинян, В. Н. Яровенко, “Прогресс в химии азот-, кислород- и серасодержащих гетероциклических систем”, Усп. хим., 89:1 (2020), 55–124  ; 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”, Russian Chem. Reviews, 89:1 (2020), 55–124 |
146
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2017 |
| 8. |
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 |
10
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2016 |
| 9. |
Е. А. Князева, О. А. Ракитин, “Влияние структурных факторов на фотовольтаические свойства сенсибилизированных красителем солнечных ячеек”, Усп. хим., 85:10 (2016), 1146–1183 ; E. A. Knyazeva, O. A. Rakitin, “Influence of structural factors on the photovoltaic properties of dye-sensitized solar cells”, Russian Chem. Reviews, 85:10 (2016), 1146–1183 |
63
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2015 |
| 10. |
L. S. Konstantinova, O. I. Bol'shakov, I. V. Baranovsky, A. M. Bogacheva, V. V. Strunyasheva, O. A. Rakitin, “A short and efficient synthesis of 5,5' -bi-1,2,3-dithiazoles”, Mendeleev Commun., 25:6 (2015), 427–428 |
11
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| 11. |
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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2014 |
| 12. |
Л. С. Константинова, О. А. Ракитин, “Монохлорид серы в органическом синтезе”, Усп. хим., 83:3 (2014), 225–250 ; L. S. Konstantinova, O. A. Rakitin, “Sulfur monochloride in organic synthesis”, Russian Chem. Reviews, 83:3 (2014), 225–250 |
23
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2012 |
| 13. |
В. А. Огурцов, О. А. Ракитин, “Реакционная способность 1,2-дитиолов”, Усп. хим., 81:7 (2012), 638–661 ; V. A. Ogurtsov, O. A. Rakitin, “Reactivity of 1,2-dithioles”, Russian Chem. Reviews, 81:7 (2012), 638–661 |
11
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2011 |
| 14. |
S. A. Amelichev, A. S. Shashkov, I. V. Zavarzin, O. A. Rakitin, “Synthesis of 17-(1,2,3-dithiazole) androstene derivatives”, Mendeleev Commun., 21:4 (2011), 186–187 |
10
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| 15. |
О. А. Ракитин, “Стабильные гетероциклические радикалы”, Усп. хим., 80:7 (2011), 679–692 ; O. A. Rakitin, “Stable heterocyclic radicals”, Russian Chem. Reviews, 80:7 (2011), 647–659 |
45
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2010 |
| 16. |
L. S. Konstantinova, M. A. Bastrakov, A. M. Starosotnikov, I. V. Glukhov, K. A. Lysov, O. A. Rakitin, S. A. Shevelev, “4,6-Dinitrobenzo[c]isothiazole: synthesis and 1,3-dipolar cycloaddition to azomethine ylide”, Mendeleev Commun., 20:6 (2010), 353–354 |
21
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| 17. |
V. A. Ogurtsov, Yu. V. Karpychev, D. A. Pestravkina, P. A. Belyakov, Yu. V. Nelyubina, O. A. Rakitin, “Synthesis of 2-iminothiophen-3(2H)-ones from 3H-1,2-dithiol-3-ones”, Mendeleev Commun., 20:5 (2010), 282–284 |
5
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| 18. |
V. V. Popov, S. A. Amelichev, L. S. Konstantinova, I. V. Glukhov, K. A. Lyssenko, O. A. Rakitin, “[(4-Sulfanylidene-4H-1λ<sup>4</sup>,3,2-dithiazol-5-yl)sulfanyl]formic acid derivatives: synthesis from 5-oxo[1,3]dithiolo[4,5-d][1,3,2]dithiazol-1-ium chloride and structural characterization”, Mendeleev Commun., 20:5 (2010), 279–281 |
1
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| 19. |
O. A. Bol'shakov, L. S. Konstantinova, R. R. Aysin, N. V. Obruchnikova, E. D. Lubuzh, O. A. Rakitin, “Unexpected formation of 5,5-diethoxy-5H-1,2,3-dithiazoles from 5H-1,2,3-dithiazole-5-thiones”, Mendeleev Commun., 20:4 (2010), 212–214 |
6
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| 20. |
S. A. Amelichev, V. V. Popov, L. S. Konstantinova, S. P. Golova, V. V. Novikov, E. D. Lubuzh, L. V. Mikhalchenko, V. P. Gul'tyai, O. A. Rakitin, “Identification of the [1,3]dithiolo[4,5-d]dithiazolyl radical”, Mendeleev Commun., 20:2 (2010), 80–82 |
5
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2009 |
| 21. |
L. S. Konstantinova, O. A. Bol'shakov, N. V. Obruchnikova, S. P. Golova, Yu. V. Nelyubina, K. A. Lyssenko, O. A. Rakitin, “Synthesis of 1,2,5-thiadiazole-3(2H)-thiones and 1,2,5-thiadiazol-3(2H)-ones from 1,2,3-dithiazoles”, Mendeleev Commun., 19:2 (2009), 84–86 |
9
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| 22. |
L. S. Konstantinova, O. A. Rakitin, “Design of sulfur heterocycles with sulfur monochloride: synthetic possibilities and prospects”, Mendeleev Commun., 19:2 (2009), 55–61 |
21
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2008 |
| 23. |
Л. С. Константинова, О. А. Ракитин, “Синтез и свойства 1,2,3-дитиазолов”, Усп. хим., 77:6 (2008), 551–577 ; L. S. Konstantinova, O. A. Rakitin, “Synthesis and properties of 1,2,3-dithiazoles”, Russian Chem. Reviews, 77:6 (2008), 521–546 |
52
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2007 |
| 24. |
Л. С. Константинова, С. А. Амеличев, О. А. Ракитин, “1,2,3,4,5-Пентатиепины и 1,2,3,4,5-пентатиепаны”, Усп. хим., 76:3 (2007), 219–236 ; L. S. Konstantinova, S. A. Amelichev, O. A. Rakitin, “1,2,3,4,5-Pentathiepines and 1,2,3,4,5-pentathiepanes”, Russian Chem. Reviews, 76:3 (2007), 195–211 |
16
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2006 |
| 25. |
S. A. Amelichev, L. S. Konstantinova, O. A. Rakitin, Ch. W. Rees, “Thienopentathiepins and pentathiepinofuran”, Mendeleev Commun., 16:6 (2006), 289–290 |
7
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2005 |
| 26. |
V. A. Ogurtsov, O. A. Rakitin, Ch. W. Rees, A. A. Smolentsev, “Synthesis of 1,3,4-thiadiazolines from 1,2-dithiole-3-thiones”, Mendeleev Commun., 15:2 (2005), 55–56 |
11
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| 27. |
V. A. Ogurtsov, O. A. Rakitin, Ch. W. Rees, A. A. Smolentsev, K. A. Lyssenko, “New routes to 1,2-dithiole-3-thiones and 3-imines”, Mendeleev Commun., 15:1 (2005), 20–21 |
6
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2004 |
| 28. |
L. S. Konstantinova, O. A. Rakitin, Ch. W. Rees, S. A. Amelichev, “Regioselective synthesis of pentathiepino-fused pyrroles and indoles”, Mendeleev Commun., 14:3 (2004), 91–92 |
22
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2003 |
| 29. |
V. A. Ogurtsov, O. A. Rakitin, Ch. W. Rees, A. A. Smolentsev, “4,5-Dichloro-1,2-dithiole-3-thione in the synthesis of benzimidazole, benzoxazole and benzothiazole derivatives of 1,3-dithioles”, Mendeleev Commun., 13:2 (2003), 50–51 |
19
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2001 |
| 30. |
L. S. Konstantinova, O. A. Rakitin, Ch. W. Rees, “Direct conversion of N-ethylamines into functionalised amides by S<sub>2</sub>Cl<sub>2</sub>”, Mendeleev Commun., 11:5 (2001), 167–168 |
8
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| 31. |
L. S. Konstantinova, O. A. Rakitin, Ch. W. Rees, “New reactions of Hünig's base with S<sub>2</sub>Cl<sub>2</sub>: formation of monocyclic 1,2-dithioles”, Mendeleev Commun., 11:5 (2001), 165–166 |
12
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1994 |
| 32. |
O. V. Zavarzina, O. A. Rakitin, L. I. Khmel'nitskii, “Substitution of the Nitro Group in Chloronitrofuroxan by N- and O-Trimethylsilyl Derivatives”, Mendeleev Commun., 4:4 (1994), 135 |
7
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1993 |
| 33. |
T. I. Godovikova, O. A. Rakitin, S. P. Golova, S. A. Vozchikova, L. I. Khmel'nitskii, “3,4-Dinitrofuroxan—the First Example of a Pernitro Heterocycle”, Mendeleev Commun., 3:5 (1993), 209–210 |
33
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1983 |
| 34. |
Т. И. Годовикова, О. А. Ракитин, Л. И. Хмельницкий, “Диазотирование в сильнокислых средах слабоосновных ароматических и гетероциклических аминов”, Усп. хим., 52:5 (1983), 777–786 ; T. I. Godovikova, O. A. Rakitin, L. I. Khmel'nitskii, “Diazotisation of Weakly Basic Aromatic and Heterocyclic Amines in Strongly Acid Media”, Russian Chem. Reviews, 52:5 (1983), 440–445 |
39
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