Mass, E. B., Duarte, G. V., Russowsky, D. (2021). The Quinazoline-Chalcone and Quinazolinone-Chalcone Hybrids: A Promising Combination for Biological Activity. Mini-Rev. Med. Chem., 197(2), 186–203. https://doi.org/10.2174/1389557520666200730160325

Kut, D., Kut, M., Komarovska-Porokhnyavets, O., Kurka, M., Onysko, M., Lubenets, V. (2024). Antimicrobial Activity of Halogen- and Chalcogen-Functionalized Thiazoloquinazolines. Lett. Drug. Des. Discov., 21(13), 2490–2496. https://doi.org/10.2174/1570180820666230726160348

Pylypenko, O.O., Sviatenko, L.K., Shabelnyk, K.P., Kovalenko, S.I., Okovytyy, S.I. (2024). Synthesis and hydrolytic decomposition of 2-hetaryl[1,2,4]triazolo[1,5-c]quinazolines: DFT study. Struct. Chem., 35(1), 97–104. https://doi.org/10.1007/s11224-023-02251-8

Antypenko, L., Antypenko, O., Karnaukh, I.,

Rebets, O., Kovalenko, S., Arisawa, M. (2023). 5,6-Dihydrotetrazolo[1,5-c]quinazolines: Toxicity prediction, synthesis, antimicrobial activity, molecular docking, and perspectives. Arch. Pharm., 356(6), 2300029. https://doi.org/10.1002/ardp.202300029

Pantyo, V.V., Haleha, O.V., Kut, D.Z., Kut, M.M., Onysko, M.Y., Danko, E.M., Koval, G.M., Pantyo, V.I., Haza, K.V., Bulyna, T.B. (2024). The effect of low-intensity laser radiation on the sensitivity of Staphylococcus aureus to some halogen-containing azaheterocycles. Regul. Mech. Biosyst., 15(2), 230–234. https://doi.org/10.15421/022434

Stavytskyi, V., Antypenko, O., Devinyak, O., Voskoboinik, O., Kovalenko, S. (2022). QSAR and pharmacophore models for screening anti-inflammatory activity among substituted (pyrrolо[1,2-a][1,2,4]triazino[2,3-c]quinazoline-5a-yl)carboxylic acids. J. Pharm. Res., 26(5), 1420–1431.

Mir, S.A., Nayak, B. (2023). Exploring binding stability of hydroxy-3-(4-hydroxyphenyl)-5-(4-nitrophenyl)-5,5a,7,8,9,9a-hexahydrothiazolo[2,3-b]quinazolin-6-one with T790M/L858R EGFR-TKD. J. Biomol. Struct. Dyn., 41, 3702–3716. https://doi.org/10.1080/07391102.2022.2053748

Mir, S. A., Mohanta, P. P., Meher, R. K., Baitharu, I., Raval, M. K., Behera, A. K., Nayak, B. (2022). Structural insights into conformational stability and binding of thiazolo-[2,3-b] quinazolinone derivatives with EGFR-TKD and in-vitro study. Saudi J. Biol. Sci., 29, 103478. https://doi.org/10.1016/j.sjbs.2022.103478

Keshari, K. A., Singh, A. K., Raj, V., Rai, A., Trivedi, P., Ghosh, B., Kumar, U., Rawat, A., Kumar, D., Saha, S. (2017). p-TSA-promoted syntheses of 5H-benzo[h] thiazolo[2,3-b]quinazoline and indeno[1,2-d]thiazolo[3,2-a]pyrimidine analogs: molecular modeling and in vitro antitumor activity against hepatocellular carcinoma. Drug Des. Dev. Ther., 11, 1623–1642. doi: 10.2147/DDDT.S136692.

Dawood, D. H., Jasass, R. S., Amin, M. M., Farghaly, T. A., Abbas, E. M. H. (2017). Synthesis of Some New Azoloazines with Potent Anti-inflammatory and Analgesic Activity. J. Heterocycl. Chem., 54, 1578–1589. https://doi.org/10.1002/jhet.2746

Panneerselvam, T., Arumugam, S., Selvaraj, K., Sankarganesh, A., Indhumathy, M., Sivakumar, A. (2017). Design, Network Analysis, In silico Modeling and Synthesis of Biologically Active Thiazolo Quinazoline Scaffolds as Anti-tubercular Agent. Curr. Chem. Biol., 11, 140–149. https://doi.org/10.2174/2212796811666170615131140

Mir, S. A., Dash, G. C., Meher, R. K., Mohanta, P.P., Chopdar, K. S., Mohapatra, P. K., Baitharu, I., Behera, A. K., Raval, M.K., Nayak, B. (2022). In Silico and In Vitro Evaluations of Fluorophoric Thiazolo-[2,3-b]quinazolinones as Anti-cancer Agents Targeting EGFR-TKD. Appl. Biochem. Biotechnol., 194, 4292–4318. https://doi.org/10.1007/s12010-022-03893-w

Kut, M. M., Onysko, M. Y. (2021). Synthesis of functionalized azolo(azino)quinazolines by electrophilic cyclization (microreview). Chem. Heterocycl. Comp., 57(5), 528–530. https://doi.org/10.1007/s10593-021-02937-z

Kut, D. Zh., Kut, М. М., Ostapchuk, Є. М., Onysko, М. Yu. (2023). [Regio- and stereo-selective halogen-induced cyclization of terminal alkynyl thioethers of 3-phenylquinazoline-4-one]. Voprosy khimii i khimicheskoi technologii – Issues of Chemistry and Chemical Technology, (6), 124–128 (in Ukrainian). http://dx.doi.org/10.32434/0321-4095-2023-151-6-124-128

Zborovskyi, Y.L., Orysik, V.V., Dobosh, O.O., Hrypak, S.M., Nesterenko, O.M., Stanynets V.I. (2002). [Synthesis of thiazolo- and thiazino[3,2-a]quinazoline derivatives]. Ukrainskii khimicheskii zhurnal – Ukrainian Chemistry Journal, 68(12), 95–99 (in Ukrainian).

Kut, D., Kut, M., Svalyavin, O., Onysko, M., Lendel, V. (2022). Halogenoheterocyclization of terminal and internal 2-allylthio-3-methyl(phenyl)-7-trifluoromethylquinazolin-4-ones. Phosphorus Sulfur Silicon Relat. Elem., 197(12), 1255–1262. https://doi.org/10.1080/10426507.2022.2085275

Vaskevych, R.I., Savinchuk, N.O., Vaskevych, A.I., Rusanov, E. B., Bylina, D. V. Kyrylchuk, A.A., Vovk, M.V. (2022). Proton- and halogen-induced cyclizations of 2-(3-butenyl)quinazolin-4(3H)-ones in the synthesis of pyrrolo[2,1-b]- and pyrrolo[1,2-а]quinazolinone derivatives. J. Heterocycl. Chem., 60(3), 431–448. https://doi.org/10.1002/jhet.4598

Vaskevych, A. I., Savinchuk, N. O., Vaskevych, R. I., Rusanov, E. B., Grygorenko, O. O., Vovk, M. V. (2021). The PIFA-initiated oxidative cyclization of 2-(3-butenyl)quinazolin- 4(3H)-ones - an efficient approach to 1-(hydroxymethyl)- 2,3-dihydropyrrolo[1,2-a]quinazolin-5(1H)-ones. Beilstein J. Org. Chem., 17, 2787–2794. https://doi.org/10.3762/bjoc.17.189

Vaskevych, A. I., Savinchuk, N. O., Vaskevych, R. I., Rusanov, E. B., Vovk, M. V. (2022). Chalcogenation/pyrrolo(pyrido)annulation of 2-(3-butenyl)quinazolin-4(3H)-ones by arylsulfenyl(selenyl) chlorides. Tetrahedron, 111, 132722. https://doi.org/10.1016/j.tet.2022.132722

Kut, D. Z., Kut, M. M., Ostapchuk, E. M., Onysko, M. Yu, Onys’ko, P. P., Lendel, V. G. (2024). Versatile synthesis of 2-functionalized dihydrothiazolo[2,3-b]quinazolines through regioselective electrophilic intramolecular heterocyclization of 3-alkenyl-2-thioxoquinazolin-4-ones. Phosphorus Sulfur Silicon Relat. Elem., Accepted. https://doi.org/10.1080/10426507.2024.2416210

Gurnani, C., Jura, M., Levason, W., Ratnani, R., Reid, G., Webster, M. (2009). Preparation and structures of tellurium(IV) halide complexes with thioether coordination. Dalton Trans., (21), 4122–4128. https://doi.org/10.1039/B902771H

Kut, D. Zh., Kut, М. М., Onysko, М. Yu., Lendel, V.G. (2021). [Electrophilic cyclization of propargyl thioethers of 3-methyl(phenyl)-2-(prop-2-yn- 1-ylthio)-7-(trifluoromethyl)quinazolin-4(3H)-ones by tellurium tetrahalides]. Voprosy khimii i khimicheskoi technologii – Issues of Chemistry and Chemical Technology, (6), 124–128 (in Ukrainian). http://dx.doi.org/10.32434/0321-4095-2021-139-6-40-44

Slivka, M., Korol, N., Pantyo, V., Baumer, V., Lendel, V. (2017). Regio- and stereoselective synthesis of [1,3]thiazolo[3,2-b][1,2,4]triazol-7-ium salts via electrophilic heterocyclization of 3-S-propargylthio-4Н-1,2,4-triazoles and their antimicrobial activity. Heterocycl Commun., 23(2), 109–113. https://doi.org/10.1515/hc-2016-0233

Slivka, M., Fizer, M., Mariychuk, R., Ostafin, M., Moyzesh, O., Koval, G., Holovko-Kamoshenkova, O., Rusyn, I., Lendel, V. (2024). Synthesis and Antimicrobial Activity of Functional Derivatives of thiazolo[ 2,3-c][1,2,4]triazoles. Lett. Drug. Des. Discov., 19(9), 791–799. https://doi.org/10.2174/1570180819666220110145659

Paegle, Е., Belyakov, S., Petrova, M., Liepinsh, E., Arsenyan, P. (2015). Cyclization of Diaryl(hetaryl)alkynes under Selenobromination Conditions: Regioselectivity and Mechanistic Studies. Eur. J. Org. Chem., 2015(20), 4389–4399. https://doi.org/10.1002/ejoc.201500431