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Публикации в базе данных Math-Net.Ru |
Цитирования |
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2020 |
1. |
M. A. Grin, N. V. Suvorov, A. F. Mironov, “Natural chlorins as a promising platform for creating targeted theranostics in oncology”, Mendeleev Commun., 30:4 (2020), 406–418 |
12
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2019 |
2. |
N. V. Suvorov, D. A. Cheskov, A. F. Mironov, M. A. Grin, “Inverse electron demand Diels–Alder reaction as a novel method for functionalization of natural chlorins”, Mendeleev Commun., 29:2 (2019), 206–208 |
8
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2018 |
3. |
K. A. Zhdanova, A. V. Ezhov, N. A. Bragina, A. F. Mironov, “Synthesis of new binary porphyrin–cyanine conjugates and their self-aggregation in organic-aqueous media”, Mendeleev Commun., 28:6 (2018), 626–628 |
5
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4. |
M. A. Gradova, I. I. Ostashevskaya, O. V. Gradov, A. V. Lobanov, V. S. Lebedeva, A. F. Mironov, “Photophysical properties and photodynamic activity of 13,15-N-methoxy-cycloimide chlorin p<sub>6</sub> methyl ester in micellar surfactant solutions”, Mendeleev Commun., 28:6 (2018), 589–591 |
5
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5. |
А. Ф. Миронов, К. А. Жданова, Н. А. Брагина, “Наноразмерные средства доставки фотосенсибилизаторов для диагностики и фотодинамической терапии в онкологии”, Усп. хим., 87:9 (2018), 859–881 ; A. F. Mironov, K. A. Zhdanova, N. A. Bragina, “Nanosized vehicles for delivery of photosensitizers in photodynamic diagnosis and therapy of cancer”, Russian Chem. Reviews, 87:9 (2018), 859–881 |
41
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2017 |
6. |
M. A. Grin, S. S. Brusov, E. Yu. Shchepelina, Ph. V. Ponomarev, M. K. Khrenova, A. A. Smirnov, V. S. Lebedeva, A. F. Mironov, “Conjugates of natural chlorins with cyclen as chelators of transition metals”, Mendeleev Commun., 27:4 (2017), 338–340 |
5
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7. |
O. I. Gushchina, V. A. Gramma, E. A. Larkina, A. F. Mironov, “Incorporation of hydrophobic chlorin photosensitizers into a liposome membrane”, Mendeleev Commun., 27:1 (2017), 50–52 |
6
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2016 |
8. |
А. А. Друзина, В. И. Брегадзе, А. Ф. Миронов, А. А. Семиошкин, “Cинтез конъюгатов полиэдрических гидридов бора с нуклеозидами”, Усп. хим., 85:11 (2016), 1229–1254 ; A. A. Druzina, V. I. Bregadze, A. F. Mironov, A. A. Semioshkin, “Synthesis of conjugates of polyhedral boron hydrides with nucleosides”, Russian Chem. Reviews, 85:11 (2016), 1229–1254 |
22
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9. |
Н. А. Брагина, К. А. Жданова, А. Ф. Миронов, “Синтез, свойства и самоорганизация мезо-арилпорфиринов с высшими алкильными заместителями”, Усп. хим., 85:5 (2016), 477–512 ; N. A. Bragina, K. A. Zhdanova, A. F. Mironov, “Synthesis, properties and self-organization of meso-arylporphyrins with higher alkyl substituents”, Russian Chem. Reviews, 85:5 (2016), 477–512 |
13
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2015 |
10. |
V. S. Lebedeva, F. M. Karmova, A. F. Mironov, “Alkylation of Chlorin p<sub>6</sub> N-hydroxycycloimide with the use of 1,8-diazabicyclo[5.4.0]undec-7-ene”, Mendeleev Commun., 25:2 (2015), 117–118 |
4
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11. |
V. S. Lebedeva, F. M. Karmova, Ph. V. Toukach, A. F. Mironov, “Synthesis of donor–acceptor systems based on the derivatives of chlorophyll a and [60]fullerene”, Mendeleev Commun., 25:1 (2015), 32–33 |
4
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2014 |
12. |
K. A. Zhdanova, N. A. Bragina, V. N. Bagratashvili, P. S. Timashev, A. F. Mironov, “Noncovalent assemblies of CdSe semiconductor quantum dots and an amphiphilic long-chain meso-arylporphyrin”, Mendeleev Commun., 24:4 (2014), 247–249 |
8
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2013 |
13. |
A. V. Laptev, D. E. Pugachev, A. Yu. Lukin, A. V. Nechaev, N. E. Belikov, O. V. Demina, P. P. Levin, A. A. Khodonov, A. F. Mironov, S. D. Varfolomeev, V. I. Shvets, “Synthesis of 5,10,15,20-tetra[6' -nitro-1,3,3-trimethylspiro- (indolino-2,2' -2H-chromen-5-yl)]porphyrin and its metal complexes”, Mendeleev Commun., 23:4 (2013), 199–201 |
2
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14. |
А. Ф. Миронов, “Комплексы порфиринов с лантанидами”, Усп. хим., 82:4 (2013), 333–351 ; A. F. Mironov, “Porphyrin complexes with lanthanides”, Russian Chem. Reviews, 82:4 (2013), 333–351 |
35
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2012 |
15. |
K. A. Formirovsky, N. A. Bragina, A. F. Mironov, G. A. Ananieva, V. V. Bykova, N. V. Usol'tseva, “Synthesis and Liquid-crystal Properties of New Amphiphilic Long-chain Derivatives of Meso-arylporphyrins with Terminal Polar Groups”, Mendeleev Commun., 22:5 (2012), 278–280 |
9
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16. |
E. S. Zyablikova, N. A. Bragina, A. F. Mironov, “Covalent-bound Conjugates of Fullerene C<sub>60</sub> and Metal Complexes of Porphyrins with Long-chain Substituents”, Mendeleev Commun., 22:5 (2012), 257–259 |
8
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17. |
I. S. Lonin, M. A. Grin, A. A. Lakhina, A. F. Mironov, “Synthesis of chlorophyll a glycoconjugates using olefin cross-metathesis”, Mendeleev Commun., 22:3 (2012), 157–158 |
12
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2011 |
18. |
M. A. Grin, R. A. Titeev, D. I. Brittal, O. V. Ulybina, A. G. Tsiprovskiy, M. Ya. Berzina, I. A. Lobanova, I. B. Sivaev, V. I. Bregadze, A. F. Mironov, “New conjugates of cobalt bis(dicarbollide) with chlorophyll a derivatives”, Mendeleev Commun., 21:2 (2011), 84–86 |
29
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2010 |
19. |
N. V. Novikov, K. A. Formirovsky, N. A. Bragina, A. F. Mironov, G. A. Ananieva, V. V. Bykova, N. V. Usol'tseva, “Synthesis and mesomorphism of cationic derivatives of meso-aryl-substituted porphyrins and their metal complexes”, Mendeleev Commun., 20:4 (2010), 239–241 |
3
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20. |
V. S. Lebedeva, R. D. Ruziev, A. F. Mironov, “Synthesis of phosphorus-containing natural chlorins”, Mendeleev Commun., 20:3 (2010), 135–136 |
3
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2008 |
21. |
I. N. Fedulova, N. A. Bragina, N. V. Novikov, A. F. Mironov, V. V. Bykova, N. V. Usol'tseva, G. A. Ananieva, “Synthesis and mesomorphism of tetraphenylporphyrin derivatives”, Mendeleev Commun., 18:6 (2008), 324–326 |
9
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22. |
M. A. Grin, I. S. Lonin, A. I. Makarov, A. A. Lakhina, Ph. V. Toukach, V. V. Kachala, A. V. Orlova, A. F. Mironov, “Synthesis of chlorin–carbohydrate conjugates by ‘click chemistry'”, Mendeleev Commun., 18:3 (2008), 135–137 |
29
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2007 |
23. |
V. S. Lebedeva, R. D. Ruziev, A. V. Popov, Yu. L. Sebyakin, A. F. Mironov, “Synthesis of glycoconjugated chlorin p<sub>6</sub> cycloimide”, Mendeleev Commun., 17:4 (2007), 212–213 |
5
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24. |
M. A. Grin, I. S. Lonin, S. V. Fedyunin, A. G. Tsiprovskiy, A. A. Strizhakov, A. A. Tsygankov, A. A. Krasnovsky, A. F. Mironov, “Synthesis and properties of the Zn-chlorin–bacteriochlorin dimer”, Mendeleev Commun., 17:4 (2007), 209–211 |
14
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25. |
M. A. Grin, A. A. Semioshkin, R. A. Titeev, E. A. Nizhnik, Yu. N. Grebenyuk, A. F. Mironov, V. I. Bregadze, “Synthesis of a cycloimide bacteriochlorin p conjugate with the closo-dodecaborate anion”, Mendeleev Commun., 17:1 (2007), 14–15 |
29
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2004 |
26. |
A. F. Mironov, M. A. Grin, A. G. Tsiprovskiy, R. A. Titeev, E. A. Nizhnik, I. S. Lonin, “Synthesis of cationic bacteriochlorins”, Mendeleev Commun., 14:5 (2004), 204–207 |
15
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2003 |
27. |
A. F. Mironov, M. A. Grin, S. A. Nochovny, Ph. V. Toukach, “Novel cycloimides in the chlorophyll a series”, Mendeleev Commun., 13:4 (2003), 156–158 |
8
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2002 |
28. |
A. F. Mironov, M. A. Grin, T. V. Moskal'chuk, A. S. Shashkov, B. V. Lokshin, “Synthesis and unusual spectroscopic properties of diformyltetraarylporphyrins”, Mendeleev Commun., 12:5 (2002), 204–205 |
3
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2001 |
29. |
A. F. Mironov, M. A. Grin, D. V. Dzardanov, K. V. Golovin, Y. K. Shim, “Synthesis of a vinyl-containing analogue of bacteriochlorophyll a”, Mendeleev Commun., 11:6 (2001), 205–206 |
3
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1998 |
30. |
A. F. Mironov, V. D. Rumyantseva, O. N. Ponamoreva, “A porphyrin chlorination reaction”, Mendeleev Commun., 8:5 (1998), 187–188 |
5
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1997 |
31. |
A. F. Mironov, A. V. Efremov, O. A. Efremova, R. Bonnett, “Novel chlorins with a δ-lactone ring”, Mendeleev Commun., 7:6 (1997), 244–245 |
4
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1995 |
32. |
D. A. Ban, A. F. Mironov, “Structure of Isomeric Ether-bonded Porphyrin-Chlorins”, Mendeleev Commun., 5:4 (1995), 153–155 |
1
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33. |
E. G. Levinson, N. A. Reztsova, A. F. Mironov, “Metal Complexes of Porphyrin Dimers with Ether and C=C Bonds”, Mendeleev Commun., 5:2 (1995), 44–46 |
3
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1994 |
34. |
E. G. Levinson, A. F. Mironov, “Synthesis and Properties of Metal Complexes of Ether-bonded Porphyrin–Chlorin Dimer”, Mendeleev Commun., 4:3 (1994), 94–95 |
2
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1993 |
35. |
G. B. Maravin, A. F. Mironov, “Synthesis of Chromophores Based on Porphyrins and Open-chain Polypyrroles”, Mendeleev Commun., 3:3 (1993), 104–107 |
2
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1992 |
36. |
E. G. Levinson, A. N. Nizhnik, A. F. Mironov, “Regiospecific Synthesis of Oligomeric Porphyrins: Ether-bonded Porphyrin–Chlorins”, Mendeleev Commun., 2:3 (1992), 95–96 |
6
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