1. Mayoka, G., Keiser, J., Häberli, C. & Chibale K. (2019) Structure–Activity Relationship and in Vitro Absorption, Distribution, Metabolism, Excretion, and Toxicity (ADMET) Studies of N-aryl 3-Trifluoromethyl Pyrido[1,2-a]benzimidazoles That Are Efficacious in a Mouse Model of Schistosomiasis, ACS Infect. Dis., 5, pp. 418–429. DOI:https://doi.org/10.1021/acsinfecdis.8b00313.
2. Liu, A., Ji, R., Shen, S., Cao, X. & Ge,Y. (2017) A ratiometric fluorescent probe for sensing sulfite based on a pyrido [1, 2-a] benzimidazole fluorophore, New Journal of Chemistry, 41(18), pp. 10096-10100. DOI:https://doi.org/10.1039/C7NJ02086D.
3. Gadde, S., Kleynhans, A., Holien, J.K., Bhadbhade, M., Nguyen, P.L.D., Mittra, R., Yu, T.T., Carter, D.R., Parker, M.W., Marshall, G.M., Cheung, B.B. & Kumar, N. (2023) Pyrimido[1,2-a]benzimidazoles as inhibitors of oncoproteins ubiquitin specific protease 5 and MYCN in the childhood cancer neuroblastoma, Bioorg Chem., 136, 106462. DOI:https://doi.org/10.1016/j.bioorg.2023.106462.
4. Kotovskaya, S.K., Baskakova, Z.M., Charushin, V.N., Chupakhin, O.N., Belanov, E.F., Bormotov, N.I., Balakhnin, S.M. & Serova, O.A. (2005) Synthesis and antiviral activity of fluorinated pyrido[1,2 a]benzimidazoles, Him.-farm. Zhurnal, 39(11), pp. 12–16. DOI:https://doi.org/10.30906/0023-1134-2005-39-11-12-16 (in Russian).
5. Arutyunyan, A.A., Avakimyan, J.A. & Stepanyan, G.M. (2016) Antibacterial properties of some polycyclic heterocycles based on pyrimidine and benzimidazole, Biologicheskij zhurnal Armenii, 68(2), pp. 88-91 [online]. Available at: https://arar.sci.am/dlibra/publication/260297 (accessed 02.02.2024) (in Russian).
6. Koo, H.L. & Dupont, H.L. (2010) Rifaximin: A Unique Gastrointestinal-Selective Antibiotic for Enteric Diseases, Curr. Opin. Gastroenterol., 26, pp. 17–25. DOI:https://doi.org/10.1097/MOG.0b013e328333dc8d.
7. Begunov, R.S., Egorov, D.O., Chetvertakova, A.V., Savina, L.I. & Zubishina, A.A. (2023) Antibacterial Activity of the Halogen- and Nitro Derivatives of Benzimidazole Against Bacillus Subtilis, Antibiotiki i khimioterapiya, 68(3-4), pp. 19-24. DOI:https://doi.org/10.37489/0235-2990-2023-68-3-4-19-24 (in Russian).
8. Andrzejewska, M., Yépez-Mulia, L., Cedillo-Rivera, R., Tapia, A., Vilpo, L., Vilpo, J. & Kazimierczuk, Z. (2002) Synthesis, antiprotozoal and anticancer activity of substituted 2-trifluoromethyl- and 2 pentafluoroethylbenzimidazoles, European Journal of Medicinal Chemistry, 37, pp. 973–978. DOI:https://doi.org/10.1016/S0223-5234(02)01421-6.
9. Tkachenko, P.V., Tkachenko, E.V., Zhuravel, I.A., Kazmirchuk, V.V. & Derbisbekova, U.B. (2017) Synthesis and antimicrobial activity 4-arylsulphonyl-derivatives 5-aminopyrazoles, Vestnik KazNMU, (2), pp. 307–311 [online]. Available at: https://cyberleninka.ru/article/n/sintez-i-protivimikrobnaya-aktivnost-4-arilsulfonilproizvodnyh-5-aminopirazolov (accessed 12.02.2024) (in Russian).
10. Begunov, R.S., Sokolov, A.A., Belova, V.O., Fakhrutdinov, A.N., Shashkov, A.S. & Fedyanin, I.V. (2015) Reaction of substituted pyrido[1,2-a]benzimidazoles with electrophilic agents, Tetrahedron Letters, 56(42), pp. 5701–5704. DOI:https://doi.org/10.1016/j.tetlet.2015.08.014.
11. Begunov, R.S., Ryzvanovich, G.A. & Firgang, S.I. (2004) Simple method for the synthesis of substituted benzo[4,5]imidazo[1,2-a]pyridines, Zhurnal organicheskoj khimii, 40(11), pp. 1740-1742. DOI:https://doi.org/10.1007/s11178-005-0082-5 (in Russian).
12. Bogdanova, D.M., Savina, L.I. & Begunov, R.S. (2022) Synthesis and functionalization of pyrido[1,2 a]benzimidazole amino derivatives, From Chemistry Towards Technology Step-By-Step, 3(4), pp. 30 38 [online]. Available at: http://chemintech.ru/index.php/tor/2022-3-4 (in Russian) (accessed 10.12.2023).
13. Becke, A. D. (1993) Density-functional thermochemistry. III. The role of exact exchange, J. Chem. Phys., 98(7), pp. 5648-5652. DOI:https://doi.org/10.1063/1.464913.
14. Miehlich, B.A., Savin, H.S., Stoll, H. & Preuss, H. (1989) Results Obtained with the Correlation Energy Density Functionals of Becke and Lee, Yang and Parr, Chemical Physics Letters, 157(3), pp. 200-206. DOI:https://doi.org/10.1016/0009-2614(89)87234-3.
15. Mueller, M. (2001) Fundamentals of Quantum Chemistry. Molecular Spectroscopy and Modern Electronic Structure Computation, International Journal of Molecular Sciences, 2(6), pp. 291-292. DOI:https://doi.org/10.3390/i2060291.
16. Granovsky, A.A. (2024) Firefly version 8.8 [online]. Available at: http://classic.chem.msu.su/gran/firefly/index.html (accessed 20.02.2024).
17. Neese, F. (2012) The ORCA program system, Wiley Interdisciplinary Reviews: Computational Molecular Science, 2(1), pp. 73–78. DOI:https://doi.org/10.1002/wcms.81.
18. Fukui, K., Yonezawa, T. & Nagata, C. (1957) MO-Theoretical Approach to the Mechanism of Charge Transfer in the Process of Aromatic Substitutions, Bulletin of the Chemical Society of Japan, 27, pp. 1247–1256. DOI:https://doi.org/10.1063/1.1743986.
19. Breza, M. & Milata, V. (2005) Quantum-chemical studies of the nitration of benzazoles, ARKIVOC, 9, pp. 80 89. DOI:https://doi.org/10.3998/ark.5550190.0006.909.
20. Bode, B.M. & Gordon, M.S. (1998) MacMolPlt: a graphical user interface for GAMESS, J. Mol. Graphics and Modeling, 16(3), pp. 133-138. DOI:https://doi.org/10.1016/s1093-3263(99)00002-9).
21. Zhurko, G.A. (2024) Chemcraft. Version 1.6 [online]. Available at: http://www.chemcraftprog.com (accessed at 12.02.2024).