Nucleophilic dearomatization of 4-aza-6-nitrobenzofuroxan by CH acids in the synthesis of pharmacology-oriented compounds

Scholarly Works

• Ivanova, V. V.; Starosotnikov, A. M.; Minyaev, M. E.; Kruchinin, A. A.; Fakhrutdinov, A. N.; Bastrakov, M. A. C-H functionalization of highly electrophilic azolopyridines as a way to donor-acceptor conjugated indoles. Mendeleev Communications 2025, 35, 648–650. doi:10.71267/mencom.7793
• Starosotnikov, A.; Bastrakov, M. Nitropyridines in the Synthesis of Bioactive Molecules. Pharmaceuticals (Basel, Switzerland) 2025, 18, 692. doi:10.3390/ph18050692
• Kolyadina, S. A.; Bastrakov, M. A.; Starosotnikov, A. M. Synthesis of new mono- and dinitroimidazo[1,2-a]pyridines. Russian Chemical Bulletin 2025, 74, 115–119. doi:10.1007/s11172-025-4506-9
• Egorov, M. P.; Ananikov, V. P.; Baskir, E. G.; Boganov, S. E.; Bogdan, V. I.; Vereshchagin, A. N.; Vil', V. A.; Dalinger, I. L.; Dilman, A. D.; Eliseev, O. L.; Zlotin, S. G.; Knyazeva, E. A.; Kogan, V. M.; Kononov, L. O.; Krayushkin, M. M.; Krylov, V. B.; Kustov, L. M.; Levin, V. V.; Lichitsky, B. V.; Medvedev, M. G.; Nifantiev, N. E.; Rakitin, O. A.; Sakharov, A. M.; Svitanko, I. V.; Smirnov, G. A.; Stakheev, A. Y.; Syroeshkin, M. A.; Terent'ev, A. O.; Tomilov, Y. V.; Tretyakov, E. V.; Trushkov, I. V.; Fershtat, L. L.; Chaliy, V. A.; Shirinian, V. Z. Current trends in organic chemistry: contribution of the N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences. Russian Chemical Bulletin 2024, 73, 2423–2532. doi:10.1007/s11172-024-4366-8
• Starosotnikov, A. M.; Bastrakov, M. A. Dinitropyridines: Synthesis and Reactions. Asian Journal of Organic Chemistry 2024, 13. doi:10.1002/ajoc.202400304
• Bastrakov, M. A.; Kruchinin, A. A.; Kolyadina, S. A.; Starosotnikov, A. M. Nitro-substituted 2-aryl-[1,2,4]triazolo[1,5-a]azines in the reactions with C-nucleophiles. Russian Chemical Bulletin 2024, 73, 1334–1341. doi:10.1007/s11172-024-4251-5
• Fedorenko, A. K.; Ivanova, V. V.; Minyaev, M. E.; Bastrakov, M. A.; Starosotnikov, A. M. A New Efficient Method for the Synthesis of Fused [1,2,5]Thiadiazoles and Their Dearomatization with C‐Nucleophiles. ChemistrySelect 2023, 8. doi:10.1002/slct.202303122
• Bastrakov, M. A.; Fedorenko, A. K. Synthesis and reactivity of furoxano[3,4-b]pyridines (microreview). Chemistry of Heterocyclic Compounds 2023, 59, 243–245. doi:10.1007/s10593-023-03187-x
• Starosotnikov, A. M.; Bastrakov, M. A.; Kokorekin, V. A. Reactions of highly electrophilic azolo[b]pyridines with polyphenols. Russian Chemical Bulletin 2023, 72, 1219–1224. doi:10.1007/s11172-023-3892-0
• Starosotnikov, A. M.; Bastrakov, M. A. Recent Developments in the Synthesis of HIV-1 Integrase Strand Transfer Inhibitors Incorporating Pyridine Moiety. International journal of molecular sciences 2023, 24, 9314. doi:10.3390/ijms24119314
• Bastrakov, M. A.; Nadykta, V. G.; Fedorenko, A. K.; Starosotnikov, A. M. Reactions of highly electrophilic 6,8-dinitro[1,2,4]triazolo[1,5-a]pyridines with C-nucleophiles. Russian Chemical Bulletin 2023, 72, 960–965. doi:10.1007/s11172-023-3860-6
• Ivanova, V. V.; Fedorenko, A. K.; Starosotnikov, A. M.; Bastrakov, M. A. Synthesis and nucleophilic dearomatization of highly electrophilic [1,2,5]selenadiazolo[3,4-b]pyridines. Russian Chemical Bulletin 2022, 71, 1826–1829. doi:10.1007/s11172-022-3596-x
• Starosotnikov, A. M.; Bastrakov, M. A.; Kokorekin, V. A. Synthesis of stable adducts of highly electrophilic nitro(het)arenes with С-nucleophiles. Russian Chemical Bulletin 2022, 71, 474–478. doi:10.1007/s11172-022-3435-0
• Starosotnikov, A. M.; Bastrakov, M. A.; Kokorekin, V. A. Stable Anionic σ-Complexes of Highly Electrophilic Aromatics and C-Nucleophiles: Synthesis and Oxidation. In The 24th International Electronic Conference on Synthetic Organic Chemistry, MDPI, 2020; pp 35 ff. doi:10.3390/ecsoc-24-08437
• Bastrakov, M. A.; Fedorenko, A. K.; Starosotnikov, A. M.; Fedyanin, I. V.; Kokorekin, V. A. Synthesis and Facile Dearomatization of Highly Electrophilic Nitroisoxazolo[4,3-b]pyridines. Molecules (Basel, Switzerland) 2020, 25, 2194. doi:10.3390/molecules25092194
• Bastrakov, M. A.; Fedorenko, A. K.; Starosotnikov, A. M. Synthesis of 6-R-isoxazolo[4,3-b]pyridines and their reactions with C-nucleophiles. Russian Chemical Bulletin 2020, 69, 394–397. doi:10.1007/s11172-020-2774-y
• Makhova, N. N.; Belen’kii, L. I.; Gazieva, G. A.; Dalinger, I. L.; Konstantinova, L. S.; Kuznetsov, V.; Kravchenko, A. N.; Krayushkin, M. M.; Rakitin, O. A.; Starosotnikov, A. M.; Fershtat, L. L.; Shevelev, S. A.; Shirinian, V. Z.; Yarovenko, V. N. Progress in the chemistry of nitrogen-, oxygen- and sulfur-containing heterocyclic systems. Russian Chemical Reviews 2020, 89, 55–124. doi:10.1070/rcr4914
• Bastrakov, M. A.; Nikol'skiy, V. V.; Starosotnikov, A. M.; Fedyanin, I. V.; Shevelev, S. A.; Knyazev, D. A. Reactions of 3-R-5-nitropyridines with nucleophiles: Nucleophilic substitution vs conjugate addition. Tetrahedron 2019, 75, 130659. doi:10.1016/j.tet.2019.130659
• Starosotnikov, A. M.; Shkaev, D. V.; Bastrakov, M. A.; Fedyanin, I. V.; Shevelev, S. A.; Dalinger, I. L. Dearomatization of oxa- or selenadiazolopyridines with neutral nucleophiles as an efficient approach to pharmacologically relevant nitrogen compounds. Mendeleev Communications 2018, 28, 638–640. doi:10.1016/j.mencom.2018.11.025

Explore citations to this article at