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Публикации в базе данных Math-Net.Ru |
Цитирования |
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2023 |
| 1. |
Z. R. Makaev, N. S. Vostrikov, N. K. Selezneva, M. S. Miftakhov, “A facile synthesis of (±)-15-deoxy-Δ<sup>12,14</sup>-prostaglandin J<sub>2</sub> methyl ester”, Mendeleev Commun., 33:4 (2023), 479–480   |
1
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2022 |
| 2. |
V. A. Egorov, L. S. Khasanova, F. A. Gimalova, A. N. Lobov, D. V. Ishmetova, V. A. Vakhitov, M. S. Miftakhov, “Cytotoxicity of novel cross-conjugated arylated cyclopentene-1,3-diones”, Mendeleev Commun., 32:2 (2022), 183–185 |
4
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2021 |
| 3. |
G. R. Sunagatullina, A. N. Lobov, M. S. Miftakhov, “Lead tetraacetate assisted formation of bis(acetoxy)acetic acid derivative from carvone”, Mendeleev Commun., 31:5 (2021), 696–697 |
| 4. |
A. M. Gimazetdinov, A. Z. Al'mukhametov, V. V. Zagitov, M. S. Miftakhov, “Formal synthesis of J-type prostaglandins based on enantiopure polyfunctional cyclopentenol derivative”, Mendeleev Commun., 31:2 (2021), 239–241 |
3
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2020 |
| 5. |
N. K. Selezneva, A. M. Galeeva, L. M. Khalilov, Z. R. Valiullina, M. S. Miftakhov, “Base-determinant chemodivergent transformations of chiral 2,3-dibromopropanamide derivative”, Mendeleev Commun., 30:3 (2020), 313–314 |
2
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| 6. |
A. Z. Al'mukhametov, A. M. Gimazetdinov, M. S. Miftakhov, “A convenient synthesis of enantiopure (4aS,7aR)-1,4,4a,7a-tetrahydrocyclopenta[c]pyran-3,7-dione”, Mendeleev Commun., 30:1 (2020), 10–11 |
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2019 |
| 7. |
N. S. Vostrikov, L. V. Spirikhin, A. N. Lobov, A. M. Gimazetdinov, Z. R. Zileeva, Yu. V. Vakhitova, Z. R. Macaev, K. K. Pivnitsky, M. S. Miftakhov, “Simple antitumor model compounds for cross-conjugated cyclopentenone prostaglandins”, Mendeleev Commun., 29:4 (2019), 372–374 |
11
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| 8. |
V. A. Egorov, F. A. Gimalova, Z. R. Zileeva, L. F. Zainullina, Yu. V. Vakhitova, M. S. Miftakhov, “2,3,5-Trichlorocyclopent-2-enone derivatives in the Friedel–Crafts reaction with methoxybenzenes and the anticancer activity of the products”, Mendeleev Commun., 29:2 (2019), 174–175 |
9
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2018 |
| 9. |
A. M. Gimazetdinov, A. Z. Al'mukhametov, V. V. Loza, L. V. Spirikhin, M. S. Miftakhov, “Enantiopure vicinally trisubstituted all-cis-bis(hydroxymethyl)-cyclopentenols and their derivatives”, Mendeleev Commun., 28:5 (2018), 546–547 |
6
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| 10. |
A. Z. Al'mukhametov, A. M. Gimazetdinov, M. S. Miftakhov, “Synthetically attractive chiral cyclopentenone building blocks conjugated with tetrahydro- and 2-oxotetrahydrofurans”, Mendeleev Commun., 28:4 (2018), 362–363 |
5
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| 11. |
S. A. Torosyan, V. V. Zagitov, F. A. Gimalova, R. Z. Biglova, M. S. Miftakhov, “Self-condensation of N-substituted (4H-thieno[3,2-b]-pyrrol-5-yl)methanols into bis(thienopyrrolyl)methanes”, Mendeleev Commun., 28:2 (2018), 192–194 |
9
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| 12. |
N. K. Selezneva, Z. R. Valiullina, L. S. Khasanova, F. A. Gimalova, R. Z. Biglova, M. S. Miftakhov, “Novel azetidinones for carbapenems and fragmentation in the allylamine precursor analogue”, Mendeleev Commun., 28:2 (2018), 131–132 |
4
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2017 |
| 13. |
V. A. Egorov, L. S. Khasanova, F. A. Gimalova, A. N. Lobov, M. S. Miftakhov, “Straightforward synthesis of pyrrolizidines”, Mendeleev Commun., 27:2 (2017), 163–165 |
3
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| 14. |
N. S. Vostrikov, I. F. Lobko, L. V. Spirikhin, Yu. V. Vakhitova, K. K. Pivnitsky, M. S. Miftakhov, “Side-modified 15-deoxy-Δ<sup>12,14</sup>-prostaglandin D<sub>2</sub>, precursor of corresponding PGJ<sub>2</sub>. Synthesis from cloprostenol and anticancer activity”, Mendeleev Commun., 27:2 (2017), 125–127 |
9
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| 15. |
N. S. Vostrikov, I. F. Lobko, Z. R. Valiullina, M. S. Miftakhov, “Synthesis of racemic Entecavir”, Mendeleev Commun., 27:1 (2017), 12–13 |
7
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2016 |
| 16. |
S. A. Torosyan, Yu. N. Biglova, F. A. Gimalova, M. S. Miftakhov, “Intermolecular disproportionation between dimethyl (2-furylmethylidene)malonate and 4-methoxybenzylamine”, Mendeleev Commun., 26:5 (2016), 429–430 |
| 17. |
Z. R. Valiullina, V. A. Akhmet'yanova, N. S. Vostrikov, M. S. Miftakhov, “A short synthesis of the carbocyclic core of Entecavir from Corey lactone”, Mendeleev Commun., 26:1 (2016), 9–10 |
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2015 |
| 18. |
Yu. N. Biglova, D. K. Susarova, A. F. Akbulatov, A. G. Mustafin, P. A. Troshin, M. S. Miftakhov, “Acrylate and methacrylate derivatives of fullerenes as electron-selective buffer layer materials for inverted organic solar cells”, Mendeleev Commun., 25:5 (2015), 348–349 |
6
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| 19. |
Yu. N. Biglova, V. V. Mikheev, S. A. Torosyan, R. Z. Biglova, M. S. Miftakhov, “Synthesis and ring-opening metathesis polymerization of fullerene-containing α,ω-bis-norbornenes”, Mendeleev Commun., 25:3 (2015), 202–203 |
6
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2014 |
| 20. |
R. F. Valeev, R. F. Bikzhanov, M. S. Miftakhov, “Synthesis of the C<sup>6</sup>–C<sup>21</sup> fragment of epothilone analogues”, Mendeleev Commun., 24:6 (2014), 372–373 |
6
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| 21. |
Z. R. Valiullina, L. S. Khasanova, N. K. Selezneva, F. A. Gimalova, K. K. Pivnitsky, M. S. Miftakhov, “Unexpected fragmentation of 16β-acetoxy-22-oxocholestanes on the action of methylenetriphenylphosphorane”, Mendeleev Commun., 24:5 (2014), 272–273 |
1
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2013 |
| 22. |
A. M. Gimazetdinov, L. A. Khalfitdinova, M. S. Miftakhov, “New α-methylidenecyclopentenone block from Corey lactone diol”, Mendeleev Commun., 23:6 (2013), 321–322 |
7
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| 23. |
Р. Б. Салихов, Ю. Н. Биглова, Ю. М. Юмагузин, Т. Р. Салихов, М. С. Мифтахов, А. Г. Мустафин, “Фотопреобразователи солнечной энергии на основе тонких пленок органических материалов”, Письма в ЖТФ, 39:19 (2013), 25–31  ; R. B. Salikhov, Yu. N. Biglova, Yu. M. Yumaguzin, T. R. Salikhov, M. S. Miftakhov, A. G. Mustafin, “Solar-energy photoconverters based on thin films of organic materials”, Tech. Phys. Lett., 39:10 (2013), 854–856 |
16
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2012 |
| 24. |
S. A. Torosyan, Yu. N. Biglova, V. V. Mikheev, Z. T. Khalitova, F. A. Gimalova, M. S. Miftakhov, “Synthesis of fullerene-containing methacrylates”, Mendeleev Commun., 22:4 (2012), 199–200 |
26
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| 25. |
V. V. Loza, N. S. Vostrikov, M. S. Miftakhov, “Efficient Resolution of Some Monoprotected Derivatives of Corey Lactone”, Mendeleev Commun., 22:3 (2012), 125–126 |
4
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2011 |
| 26. |
S. A. Torosyan, F. A. Gimalova, R. F. Valeev, M. S. Miftakhov, “Triethylsilyl triflate-promoted skeletal rearrangement of bottrospicatols”, Mendeleev Commun., 21:3 (2011), 140–141 |
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2010 |
| 27. |
R. F. Valeev, N. K. Selezneva, Z. A. Starikova, E. Yu. Pankrat'ev, M. S. Miftakhov, “Chiral building blocks from R-(–)-carvone: N-bromosuccinimidemediated addition–sceletal rearrangement of (–)-cis-carveol”, Mendeleev Commun., 20:2 (2010), 77–79 |
5
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| 28. |
A. M. Gimazetdinov, T. V. Gimazetdinova, M. S. Miftakhov, “Synthesis of enantiomeric cyclosarcomycins”, Mendeleev Commun., 20:1 (2010), 15–16 |
7
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2009 |
| 29. |
A. M. Gimazetdinov, T. V. Kolesnikova, M. S. Miftakhov, “Enantiomeric 4,4a,7,7a-tetrahydro-1H-cyclopenta[c]pyran-3-ones”, Mendeleev Commun., 19:5 (2009), 275 |
3
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| 30. |
N. K. Selezneva, F. A. Gimalova, R. F. Valeev, M. S. Miftakhov, “Synthesis of the thiazole-containing C<sup>11</sup>–C<sup>21</sup>-block of a gem-dimethylcyclopropane derivative of epothilones”, Mendeleev Commun., 19:5 (2009), 248–249 |
1
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2007 |
| 31. |
N. A. Ivanova, K. S. Kislitsina, M. S. Miftakhov, “Efficient one-pot synthesis of chlorinated cyclopentenones from hexachlorocyclopentadiene”, Mendeleev Commun., 17:5 (2007), 306–307 |
3
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2006 |
| 32. |
N. S. Vostrikov, V. Z. Vasikov, L. V. Akulova, M. S. Miftakhov, “Double α-ketol rearrangement of (1S,2R,4R)-2-acetyl-1-vinyl-2-hydroxy-7,7-dimethylbicyclo[2.2.1]heptane”, Mendeleev Commun., 16:2 (2006), 111–112 |
1
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2003 |
| 33. |
F. A. Gimalova, O. A. Gavrilov, D. G. Golovanov, V. K. Mavrodiev, M. S. Miftakhov, “New 'substitution–recyclization' reaction of a tetrachlorocyclopentadienone dimer with amines”, Mendeleev Commun., 13:5 (2003), 232–233 |
4
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| 34. |
R. V. Bikbulatov, F. A. Akbutina, L. V. Spirikhin, M. S. Miftakhov, “A 'substrate-divergent' approach to chiral cyclopentanes and cyclohexanes from a common precursor based on levoglucosan”, Mendeleev Commun., 13:3 (2003), 153–154 |
2
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| 35. |
F. A. Akbutina, I. F. Sadretdinov, N. K. Selezneva, M. S. Miftakhov, “Chiral synthetic block based on (R)-pantolactone”, Mendeleev Commun., 13:3 (2003), 151–152 |
5
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2000 |
| 36. |
Е. В. Горобец, М. С. Мифтахов, Ф. А. Валеев, “Тандемные превращения, инициируемые и определяемые реакцией Михаэля”, Усп. хим., 69:12 (2000), 1091–1110 ; E. V. Gorobets, M. S. Miftakhov, F. A. Valeev, “Tandem transformations initiated and determined by the Michael reaction”, Russian Chem. Reviews, 69:12 (2000), 1001–1019  |
41
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1994 |
| 37. |
M. S. Miftakhov, F. A. Valeev, I. N. Gaisina, G. A. Tolstikov, “Enantiomeric 9,11-Dideoxy-9,11-ethane Analogues of Prostaglandin Endoperoxide”, Mendeleev Commun., 4:2 (1994), 45–47 |
4
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| 38. |
М. С. Мифтахов, Ф. А. Валеев, И. Н. Гайсина, “Левоглюкозенон: свойства, реакции и использование в тонком органическом синтезе”, Усп. хим., 63:10 (1994), 922–936 ; M. S. Miftakhov, F. A. Valeev, I. N. Gaisina, “Levoglucosenone: the properties, reactions, and use in fine organic synthesis”, Russian Chem. Reviews, 63:10 (1994), 869–882 |
53
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| 39. |
М. С. Мифтахов, М. Э. Адлер, Ф. А. Акбутина, Г. А. Толстиков, “Морские простаноиды”, Усп. хим., 63:6 (1994), 543–555 ; M. S. Miftakhov, M. E. Adler, F. A. Akbutina, G. A. Tolstikov, “Marine prostanoids”, Russian Chem. Reviews, 63:6 (1994), 519–531 |
6
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1993 |
| 40. |
G. A. Tolstikov, F. A. Akbutina, F. A. Valeev, M. S. Miftakhov, “A Total Decyclisation of Jaeschkeanadiol”, Mendeleev Commun., 3:6 (1993), 253–254 |
1
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1992 |
| 41. |
G. A. Tolstikov, R. R. Akhmetvaleev, V. M. Zhurba, M. S. Miftakhov, “A Novel Approach to Carbacycline”, Mendeleev Commun., 2:1 (1992), 4–6 |
2
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1991 |
| 42. |
S. A. Ismailov, M. S. Miftakhov, G. A. Tolstikov, “Unusual Reactions of 2,3,5-Trichloro-4,4-dimethoxy-5-allylcyclopent-2-en-1-one with Amines”, Mendeleev Commun., 1:4 (1991), 149–151 |
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