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Публикации в базе данных Math-Net.Ru |
Цитирования |
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2025 |
| 1. |
A. V. Trifonov, N. O. Appazov, R. Kh. Bagautdinova, L. K. Kibardina, M. A. Pudovik, A. P. Lyubina, A. D. Voloshina, A. S. Gazizov, A. E. Tolegen, N. A. Togyzbayeva, K. Kh. Darmagambet, R. A. Turmanov, E. A. Chugunova, A. R. Burilov, “New 7-azacoumarin-3-carboxamide phosphonium salts: cytotoxicity and the Wittig olefination”, Mendeleev Commun., 35:5 (2025), 537–539   |
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2024 |
| 2. |
A. V. Trifonov, R. K. Bagautdinova, L. K. Kibardina, M. A. Pudovik, A. P. Lyubina, A. D. Voloshina, A. S. Gazizov, A. R. Burilov, “New triazole-containing 7-azacoumarin-3-carboxamides: synthesis and biological properties”, Mendeleev Commun., 34:5 (2024), 688–690  |
3
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2021 |
| 3. |
L. K. Kibardina, A. V. Trifonov, A. B. Dobrynin, M. A. Pudovik, A. R. Burilov, A. D. Voloshina, A. G. Strelnik, A. S. Gazizov, “Anticancer activity of novel 3-azaxanthenes”, Mendeleev Commun., 31:5 (2021), 664–666 |
3
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| 4. |
А. В. Смолобочкин, А. С. Газизов, А. Р. Бурилов, М. А. Пудовик, О. Г. Синяшин, “Успехи в синтезе гетероциклов, содержащих эндоциклический мочевинный фрагмент”, Усп. хим., 90:3 (2021), 395–417  ; A. V. Smolobochkin, A. S. Gazizov, A. R. Burilov, M. A. Pudovik, O. G. Sinyashin, “Advances in the synthesis of heterocycles bearing an endocyclic urea moiety”, Russian Chem. Reviews, 90:3 (2021), 395–417 |
21
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2020 |
| 5. |
A. V. Trifonov, L. K. Kibardina, A. B. Dobrynin, A. A. Ali Akhunov, M. A. Pudovik, A. R. Burilov, “New 1-hetarylfuropyridines and chromenes based on pyridoxal and 4-hydroxycoumarin”, Mendeleev Commun., 30:6 (2020), 765–767 |
3
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2019 |
| 6. |
R. Kh. Bagautdinova, L. I. Vagapova, A. V. Smolobochkin, A. S. Gazizov, A. R. Burilov, M. A. Pudovik, A. D. Voloshina, “Synthesis of 1-(2-aminoethylsulfonyl)-2-phosphorylpyrrolidines via consecutive Arbuzov and aza-Michael reactions and their antitumor activity”, Mendeleev Commun., 29:6 (2019), 686–687 |
5
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| 7. |
А. В. Смолобочкин, А. С. Газизов, А. Р. Бурилов, М. А. Пудовик, О. Г. Синяшин, “Реакции азотсодержащих гетероциклических соединений, протекающие с раскрытием кольца”, Усп. хим., 88:11 (2019), 1104–1127 ; A. V. Smolobochkin, A. S. Gazizov, A. R. Burilov, M. A. Pudovik, O. G. Sinyashin, “Ring opening reactions of nitrogen heterocycles”, Russian Chem. Reviews, 88:11 (2019), 1104–1127 |
28
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2018 |
| 8. |
Yu. M. Sadykova, L. M. Sadikova, A. V. Zalaltdinova, A. G. Strelnik, A. R. Burilov, M. A. Pudovik, “New bicyclic phosphonates of unsymmetrical structure”, Mendeleev Commun., 28:6 (2018), 655–656 |
4
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| 9. |
L. K. Kibardina, A. V. Trifonov, A. B. Dobrynin, M. A. Pudovik, A. R. Burilov, “Synthesis of 1-(hydroxyaryl)furo[3,4-c]pyridines from 1-amino(alkoxy)furo[3,4-c]pyridines and (poly)phenols”, Mendeleev Commun., 28:5 (2018), 551–552 |
5
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| 10. |
L. I. Vagapova, J. K. Voronina, V. V. Syakaev, A. R. Burilov, A. R. Garyfzyanov, M. A. Pudovik, “Synthesis and structure of new 2-aryl-substituted pyrrolidines containing phosphine oxide group”, Mendeleev Commun., 28:4 (2018), 398–400 |
6
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2017 |
| 11. |
I. R. Mironova (Knyazeva), D. K. Abdrafikova, K. M. Mukhamedyanova, V. V. Syakaev, B. M. Gabidullin, A. T. Gubaidullin, W. D. Habicher, A. R. Burilov, M. A. Pudovik, “Synthesis of novel highly functionalized triazole-linked calix[4]resorcinols via click reaction”, Mendeleev Commun., 27:6 (2017), 556–558 |
12
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| 12. |
I. R. Mironova (Knyazeva), V. I. Matveeva, W. D. Habicher, V. V. Syakaev, B. M. Gabidullin, A. T. Gubaidullin, A. R. Burilov, M. A. Pudovik, “New phosphorus-containing calix[4]pyridine based on para-thiophosphorylated derivative of benzaldehyde”, Mendeleev Commun., 27:3 (2017), 287–289 |
2
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| 13. |
А. С. Газизов, А. Р. Бурилов, М. А. Пудовик, О. Г. Синяшин, “Реакции азотсодержащих ацеталей с ароматическими нуклеофилами”, Усп. хим., 86:1 (2017), 75–98 ; A. S. Gazizov, A. R. Burilov, M. A. Pudovik, O. G. Sinyashin, “Reactions of nitrogen-containing acetals with aromatic nucleophiles”, Russian Chem. Reviews, 86:1 (2017), 75–98 |
11
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2013 |
| 14. |
И. Р. Князева, А. Р. Бурилов, М. А. Пудовик, В. Д. Хабихер, “Фосфорсодержащие макроциклические соединения: синтез и свойства”, Усп. хим., 82:2 (2013), 150–186 ; I. R. Knyazeva, A. R. Burilov, M. A. Pudovik, W. D. Habicher, “Phosphorus-containing macrocyclic compounds: synthesis and properties”, Russian Chem. Reviews, 82:2 (2013), 150–186 |
40
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2012 |
| 15. |
L. I. Vagapova, A. F. Fahertdinova, A. R. Burilov, M. A. Pudovik, “Synthesis of New calix[4]resorcinols with [N-diethoxyphosphorylmethyl-N-(2,2-dimethoxyethyl)amino]methyl Substituents at the Upper Rim”, Mendeleev Commun., 22:6 (2012), 325–326 |
5
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2011 |
| 16. |
L. I. Vagapova, A. R. Burilov, M. A. Pudovik, V. V. Syakaev, W. D. Habicher, A. I. Konovalov, “New calix[4]resorcinols with diarylmethane fragments on the upper rim of the molecule”, Mendeleev Commun., 21:1 (2011), 44–45 |
7
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2010 |
| 17. |
M. A. Pudovik, L. K. Kibardina, S. A. Terent'eva, A. R. Burilov, O. N. Kataeva, G. A. Chmutova, Sh. K. Latypov, O. G. Sinyashin, V. A. Alfonsov, “Stereospecific cascade cyclization reaction with the formation of tetracyclic hexacoordinated phosphorus derivatives”, Mendeleev Commun., 20:4 (2010), 226–228 |
7
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2008 |
| 18. |
A. R. Burilov, M. S. Khakimov, A. S. Gazizov, M. A. Pudovik, V. V. Syakaev, D. B. Krivolapov, A. I. Konovalov, “Reactions of resorcinol derivatives with 1-methyl-3-phenylimidazol-2-one as a new method for the synthesis of 5-arylimidazolidin-2-ones”, Mendeleev Commun., 18:1 (2008), 54–55 |
10
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2007 |
| 19. |
L. K. Kibardina, M. A. Pudovik, V. A. Alfonsov, O. N. Kataeva, “Synthesis of enantiopure 1,3,4-thiazaphospholes”, Mendeleev Commun., 17:6 (2007), 323–324 |
1
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2005 |
| 20. |
A. R. Burilov, A. S. Gazizov, Yu. M. Volodina, M. A. Pudovik, W. D. Habicher, I. Bauer, A. T. Gubaidullin, I. A. Litvinov, A. I. Konovalov, “Unusual reactions of resorcinol and methylresorcinol with methylaminoacetaldehyde dimethyl acetal”, Mendeleev Commun., 15:4 (2005), 153–154 |
12
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1996 |
| 21. |
E. Kh. Kazakova, A. I. Konovalov, L. V. Snegur, V. N. Babin, Yu. S. Nekrasov, M. A. Pudovik, “Interaction of resorcinol–octanal cyclotetramer with bis(N,N-diethylamido)menthylphosphite”, Mendeleev Commun., 6:4 (1996), 157–159 |
7
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1994 |
| 22. |
Р. А. Черкасов, М. А. Пудовик, “Гетерофосфацикланы в органическом синтезе”, Усп. хим., 63:12 (1994), 1087–1113 ; R. A. Cherkasov, M. A. Pudovik, “Heterophosphacyclanes in organic synthesis”, Russian Chem. Reviews, 63:12 (1994), 1019–1045 |
84
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1983 |
| 23. |
М. А. Пудовик, В. В. Овчинников, Р. А. Черкасов, А. Н. Пудовик, “Реакционная способность 1,3,2-дигетерофосфацикланов, содержащих трехкоординированный атом фосфора”, Усп. хим., 52:4 (1983), 640–668 ; M. A. Pudovik, V. V. Ovchinnikov, R. A. Cherkasov, A. N. Pudovik, “The Reactivity of 1,3,2-Diheterophospholans Containing a Tricoordinate Phosphorus Atom”, Russian Chem. Reviews, 52:4 (1983), 361–376 |
15
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1982 |
| 24. |
Р. А. Черкасов, В. В. Овчинников, М. А. Пудовик, А. Н. Пудовик, “Реакционная способность 1,3,2-дигетерофосфоланов и -фосфоринанов с четырехкоординированным атомом фосфора”, Усп. хим., 51:8 (1982), 1305–1336 ; R. A. Cherkasov, V. V. Ovchinnikov, M. A. Pudovik, A. N. Pudovik, “The Reactivity of 1,3,2-Diheterophospholans and 1,3,2-Diheterophosphorinanes with a Tetracoordinate Phosphorus Atom”, Russian Chem. Reviews, 51:8 (1982), 746–764 |
16
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