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Публикации в базе данных Math-Net.Ru |
Цитирования |
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2024 |
| 1. |
S. Santra, Д. С. Копчук, И. С. Ковалев, Л. К. Садиева, И. Л. Никонов, Я. К. Штайц, Г. В. Зырянов, A. Majee, A. Hajra, В. Н. Чарушин, B. C. Ranu, “Пилларарены как носители катализаторов — краткий обзор”, Усп. хим., 93:12 (2024), RCR5139  ; S. Santra, D. S. Kopchuk, I. S. Kovalev, L. K. Sadieva, I. L. Nikonov, Ya. K. Shtaitz, G. V. Zyryanov, A. Majee, A. Hajra, V. N. Charushin, B. C. Ranu, “Pillararenes as catalyst carriers: a brief update”, Russian Chem. Reviews, 93:12 (2024), RCR5139   |
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2023 |
| 2. |
A. Mukherjee, S. Mahato, Д. С. Копчук, S. Santra, Г. В. Зырянов, A. Majee, О. Н. Чупахин, “Синтез α-аминокарбонильных соединений: краткий обзор”, Усп. хим., 92:3 (2023), RCR5046  ; A. Mukherjee, S. Mahato, D. S. Kopchuk, S. Santra, G. V. Zyryanov, A. Majee, O. N. Chupakhin, “Synthesis of α-amino carbonyl compounds: a brief review”, Russian Chem. Reviews, 92:3 (2023), RCR5046 |
6
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2022 |
| 3. |
A. P. Krinochkin, M. R. Guda, A. Rammohan, D. S. Kopchuk, I. L. Nikonov, E. D. Ladin, S. Santra, I. N. Egorov, G. V. Zyryanov, O. N. Chupakhin, “Synthesis of 2-amino-3,6-di(het)arylpyridines from 5-cyano-3,6-di(het)aryl-1,2,4-triazines and arylhydrazines via the
$\mathrm{S_N^{ipso}}$/aza-Diels–Alder reaction sequence”, Mendeleev Commun., 32:6 (2022), 726–728 |
3
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| 4. |
A. Mukherjee, D. S. Kopchuk, S. Santra, A. Majee, G. V. Zyryanov, O. N. Chupakhin, “Iron(iii) chloride-catalyzed mechanochemical cascade synthesis of highly-substituted pyrrolyl indoles”, Mendeleev Commun., 32:5 (2022), 624–626 |
7
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| 5. |
A. P. Krinochkin, E. S. Starnovskaya, M. I. Valieva, D. S. Kopchuk, S. Santra, P. A. Slepukhin, G. V. Zyryanov, A. Majee, O. N. Chupakhin, “One-pot synthesis of cyclopentane-fused 5'-aryl-4-cycloalkylamino-2,2'-bipyridines via the aza-Diels–Alder/S<sub>N</sub><sup>ipso</sup> reactions”, Mendeleev Commun., 32:4 (2022), 449–451 |
4
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2021 |
| 6. |
A. P. Krinochkin, G. M. Reddy, D. S. Kopchuk, P. A. Slepukhin, Ya. K. Shtaitz, I. A. Khalymbadzha, I. S. Kovalev, G. A. Kim, I. N. Ganebnykh, G. V. Zyryanov, O. N. Chupakhin, V. N. Charushin, “2-Aminooxazoles as novel dienophiles in the inverse demand Diels–Alder reaction with 1,2,4-triazines”, Mendeleev Commun., 31:4 (2021), 542–544 |
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2020 |
| 7. |
M. I. Savchuk, I. S. Kovalev, V. L. Rusinov, D. S. Kopchuk, A. P. Krinochkin, G. V. Zyryanov, O. N. Chupakhin, V. N. Charushin, “Rapid metal free construction of 3-positioned 2-pyridyl substituent in indoles”, Mendeleev Commun., 30:6 (2020), 712–713 |
7
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| 8. |
M. I. Savchuk, A. P. Krinochkin, A. Rammohan, A. F. Khasanov, D. S. Kopchuk, I. N. Egorov, S. Santra, G. V. Zyryanov, V. L. Rusinov, O. N. Chupakhin, “An expedient synthesis of 5-alkynyl-6-aryl-2,2′-bipyridines”, Mendeleev Commun., 30:5 (2020), 610–611 |
7
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| 9. |
G. V. Zyryanov, D. S. Kopchuk, I. S. Kovalev, S. Santra, M. Rahman, A. F. Khasanov, A. P. Krinochkin, O. S. Taniya, O. N. Chupakhin, V. N. Charushin, “Rational synthetic methods in creating promising (hetero)aromatic molecules and materials”, Mendeleev Commun., 30:5 (2020), 537–554 |
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| 10. |
A. De, S. Santra, I. S. Kovalev, D. S. Kopchuk, G. V. Zyryanov, O. N. Chupakhin, V. N. Charushin, A. Majee, “Synthesis of 2-imidazolines by co-grinding of N-tosylaziridines and nitriles”, Mendeleev Commun., 30:2 (2020), 188–189 |
6
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2019 |
| 11. |
S. Gundala, M. R. Guda, A. F. Khasanov, D. S. Kopchuk, A. P. Krinochkin, S. Santra, G. V. Zyryanov, P. Venkatapuram, J. R. Garcia, V. N. Charushin, “A PASE-based approach towards 12-(1H-1,2,3-triazol-1-yl)-indolo[2,1-a]isoquinolines via the reaction of 3-(isoquinolin-1-yl)-1,2,4-triazines with benzyne”, Mendeleev Commun., 29:4 (2019), 369–371 |
11
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| 12. |
R. F. Fatykhov, M. I. Savchuk, E. S. Starnovskaya, M. V. Bobkina, D. S. Kopchuk, E. V. Nosova, G. V. Zyryanov, I. A. Khalymbadzha, O. N. Chupakhin, V. N. Charushin, V. G. Kartsev, “Nucleophilic substitution of hydrogen–the Boger reaction sequence as an approach towards 8-(pyridin-2-yl)coumarins”, Mendeleev Commun., 29:3 (2019), 299–300 |
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2018 |
| 13. |
E. V. Nosova, T. N. Moshkina, G. N. Lipunova, I. V. Baklanova, D. S. Kopchuk, P. A. Slepukhin, V. N. Charushin, “Synthesis and photophysical studies of novel 2-[5-(4-diethylaminophenyl)thiophen-2-yl]quinazoline derivatives”, Mendeleev Commun., 28:1 (2018), 14–16 |
11
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2017 |
| 14. |
Б. А. Калинин, И. С. Ковалев, О. С. Тания, Д. С. Копчук, Г. В. Зырянов, О. Н. Чупахин, “Обнаружение малых сигналов в масс-спектрах”, ЖТФ, 87:9 (2017), 1403–1406 ; B. A. Kalinin, I. S. Kovalev, O. S. Taniya, D. S. Kopchuk, G. V. Zyryanov, O. N. Chupakhin, “Detection of small signals in mass spectra”, Tech. Phys., 62:9 (2017), 1411–1414 |
| 15. |
O. V. Shabunina, D. Yu. Kapustina, A. P. Krinochkin, G. A. Kim, D. S. Kopchuk, G. V. Zyryanov, F. Li, O. N. Chupakhin, “π-Extended fluorophores based on 5-aryl-2,2'-bipyridines: synthesis and photophysical studies”, Mendeleev Commun., 27:6 (2017), 602–604 |
15
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| 16. |
D. S. Kopchuk, A. P. Krinochkin, G. A. Kim, D. N. Kozhevnikov, “Europium complex of 5-(4-dodecyloxyphenyl)2,2'-bipyridine-6'-carboxylic acid”, Mendeleev Commun., 27:4 (2017), 394–396 |
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2016 |
| 17. |
N. V. Chepchugov, D. S. Kopchuk, I. S. Kovalev, G. V. Zyryanov, V. L. Rusinov, O. N. Chupakhin, “Convenient synthesis of α-dichloromethylpyridines from 3-trichloromethyl-1,2,4-triazines”, Mendeleev Commun., 26:3 (2016), 220–222 |
14
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| 18. |
E. V. Nosova, T. N. Moshkina, D. S. Kopchuk, G. N. Lipunova, P. A. Slepukhin, V. N. Charushin, “Cyclometallated PT<sup>II</sup> complexes of 2-(2-thienyl)-4-(cycloalkylimino)-substituted quinazolines”, Mendeleev Commun., 26:2 (2016), 129–130 |
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2015 |
| 19. |
A. F. Khasanov, D. S. Kopchuk, I. S. Kovalev, O. S. Taniya, G. V. Zyryanov, V. L. Rusinov, O. N. Chupakhin, “Reaction of lithium 2-arylethynides with 6-aryl-3-(2-pyridyl)-1,2,4-triazines as an access to 6-aryl-5-arylvinyl-3-(2-pyridyl)-1,2,4-triazines”, Mendeleev Commun., 25:5 (2015), 332–333 |
12
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| 20. |
D. S. Kopchuk, I. L. Nikonov, G. V. Zyryanov, E. V. Nosova, I. S. Kovalev, P. A. Slepukhin, V. L. Rusinov, O. N. Chupakhin, “Aryne approach towards 2,3-difluoro-10-(1H-1,2,3-triazol-1-yl)pyrido[1,2-a]indoles”, Mendeleev Commun., 25:1 (2015), 13–14 |
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| 21. |
И. С. Ковалев, Д. С. Копчук, Г. В. Зырянов, В. Л. Русинов, О. Н. Чупахин, В. Н. Чарушин, “Литийорганические соединения в реакциях нуклеофильного замещения атома водорода в ряду аренов и гетаренов”, Усп. хим., 84:12 (2015), 1191–1225 ; I. S. Kovalev, D. S. Kopchuk, G. V. Zyryanov, V. L. Rusinov, O. N. Chupakhin, V. N. Charushin, “Organolithium compounds in the nucleophilic substitution of hydrogen in arenes and hetarenes”, Russian Chem. Reviews, 84:12 (2015), 1191–1225 |
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2014 |
| 22. |
I. S. Kovalev, D. S. Kopchuk, A. F. Khasanov, G. V. Zyryanov, V. L. Rusinov, O. N. Chupakhin, “The synthesis of polyarene-modified 5-phenyl-2,2'-bipyridines via the $\mathrm{S_N^H}$ methodology and aza-Diels–Alder reaction”, Mendeleev Commun., 24:2 (2014), 117–118 |
29
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| 23. |
I. S. Kovalev, D. S. Kopchuk, G. V. Zyryanov, V. L. Rusinov, O. N. Chupakhin, “Nucleophilic dimerization of indoline under oxidative conditions”, Mendeleev Commun., 24:1 (2014), 40–41 |
2
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| 24. |
Г. В. Зырянов, Д. С. Копчук, И. С. Ковалев, Э. В. Носова, В. Л. Русинов, О. Н. Чупахин, “Хемосенсоры для обнаружения нитроароматических (взрывчатых) веществ”, Усп. хим., 83:9 (2014), 783–819 ; G. V. Zyryanov, D. S. Kopchuk, I. S. Kovalev, E. V. Nosova, V. L. Rusinov, O. N. Chupakhin, “Chemosensors for detection of nitroaromatic compounds (explosives)”, Russian Chem. Reviews, 83:9 (2014), 783–819 |
87
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2013 |
| 25. |
D. S. Kopchuk, A. F. Khasanov, I. S. Kovalev, G. V. Zyryanov, V. L. Rusinov, O. N. Chupakhin, “Unexpected reduction of the nitro group in (3-nitrophenyl)-1,2,4-triazines during their aza-Diels–Alder reaction with 1-morpholinocyclopentene”, Mendeleev Commun., 23:4 (2013), 209–211 |
23
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| 26. |
D. S. Kopchuk, I. S. Kovalev, A. F. Khasanov, G. V. Zyryanov, P. A. Slepukhin, V. L. Rusinov, O. N. Chupakhin, “A rational protocol for the synthesis of 1-(2-pyridyl)isoquinolines”, Mendeleev Commun., 23:3 (2013), 142–144 |
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