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Публикации в базе данных Math-Net.Ru |
Цитирования |
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2025 |
| 1. |
V. V. Ivanova, A. M. Starosotnikov, M. E. Minyaev, A. A. Kruchinin, A. N. Fakhrutdinov, M. A. Bastrakov, “C–H functionalization of highly electrophilic azolopyridines as a way to donor–acceptor conjugated indoles”, Mendeleev Commun., 35:6 (2025), 648–650  |
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2020 |
| 2. |
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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2018 |
| 3. |
A. M. Starosotnikov, D. V. Shkaev, M. A. Bastrakov, I. V. Fedyanin, S. A. Shevelev, I. L. Dalinger, “Dearomatization of oxa- or selenadiazolopyridines with neutral nucleophiles as an efficient approach to pharmacologically relevant nitrogen compounds”, Mendeleev Commun., 28:6 (2018), 638–640 |
20
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2016 |
| 4. |
M. A. Bastrakov, A. O. Geraseva, A. M. Starosotnikov, I. V. Fedyanin, A. A. Pavlov, B. I. Ugrak, S. A. Shevelev, “Synthesis of nitro pyrido- and dipyrido[1,4]oxazines”, Mendeleev Commun., 26:5 (2016), 383–385 |
6
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| 5. |
A. M. Starosotnikov, M. A. Bastrakov, A. A. Pavlov, I. V. Fedyanin, I. L. Dalinger, S. A. Shevelev, “Synthesis of novel polycyclic heterosystems based on 5-nitro[1,2,5]thiadiazolo[3,4-e]benzofuroxan”, Mendeleev Commun., 26:3 (2016), 217–219 |
22
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2014 |
| 6. |
M. A. Bastrakov, A. M. Starosotnikov, I. V. Fedyanin, V. V. Kachala, S. A. Shevelev, “5-Nitro-7,8-furoxanoquinoline: a new type of fused nitroarenes possessing Diels–Alder reactivity”, Mendeleev Commun., 24:4 (2014), 203–205 |
19
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2012 |
| 7. |
S. Yu. Pechenkin, A. M. Starosotnikov, M. A. Bastrakov, V. V. Kachala, S. A. Shevelev, “Synthesis of fused isoindoles via 1,3-dipolar cycloaddition of 1,3-oxazolium-5-olates (münchnones) with nitro benzazoles”, Mendeleev Commun., 22:1 (2012), 35–36 |
6
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2010 |
| 8. |
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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| 9. |
A. M. Starosotnikov, M. A. Leontieva, M. A. Bastrakov, A. V. Puchnin, V. V. Kachala, S. A. Shevelev, “Superelectrophilic nature of 4,6-dinitrobenzo[c]isoxazole (4,6-dinitroanthranil) in [4+2]-cycloaddition reactions and σ<sup>H</sup>-complex formation”, Mendeleev Commun., 20:3 (2010), 165–166 |
16
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2009 |
| 10. |
M. A. Bastrakov, A. M. Starosotnikov, M. A. Leontieva, A. Kh. Shakhnes, S. A. Shevelev, “Synthesis of polycyclic indole derivatives from 2,4,6-trinitrotoluene”, Mendeleev Commun., 19:1 (2009), 47–48 |
5
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2008 |
| 11. |
E. M. Asadulina, M. A. Bastrakov, V. V. Kachala, A. M. Starosotnikov, S. A. Shevelev, “Synthesis of 3-substituted 1,5-dinitro-3-azabicyclo-[3.3.1]nonanes containing a pyrazole fragment”, Mendeleev Commun., 18:4 (2008), 213–214 |
4
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2002 |
| 12. |
A. M. Starosotnikov, V. M. Vinogradov, S. A. Shevelev, “Synthesis of 14π-electron peri-annelated tricyclic heteroaromatic systems based on 2,4,6-trinitrotoluene”, Mendeleev Commun., 12:5 (2002), 200–202 |
6
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| 13. |
V. M. Vinogradov, A. M. Starosotnikov, S. A. Shevelev, “Synthesis and reactions of 1-aryl-3-formyl-4,6-dinitro-1H-indazoles”, Mendeleev Commun., 12:5 (2002), 198–200 |
11
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2000 |
| 14. |
V. M. Vinogradov, I. L. Dalinger, A. M. Starosotnikov, S. A. Shevelev, “Synthesis and transformations of picrylacetaldehyde”, Mendeleev Commun., 10:4 (2000), 140–141 |
13
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