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• 1. 1. Orlewska, C.; Pancechowska-Ksepko, D.; Foks, H.; Zwolska, Z.; Augustynowicz-Kopec, E. Reactivity of N 1-Dithioester Substituted Pyridinand Pyrazincarboxamidrazones. Phosphorus, Sulfur, and Silicon and the Related Elements, 2006, 181(4), pp. 737–744. https://doi.org/10.1080/10426500500270065
• 2. Pellizzari, G.; Gazz Chim Ital, 1911, no. 41, pp. 93.
• 3. Ji Ram, V.; Sethi, A.; Nath, M.; Pratap, R. Five-Membered Heterocycles. The Chemistry of Heterocycles, 2019, pp. 365. https://doi.org/10.1016/b978-0-08-101033-4.00005-x
• 4. Ueda, S.; Nagasawa, H. Facile synthesis of 1,2,4-triazoles via a copper-catalyzed tandem addition−oxidative cyclization. Journal of the American Chemical Society, 2009, 131(42), pp. 15080-15081. DOI: https://doi.org/10.1021/ja905056z
• 5. Huang, H.; Guo, W.; Wu, W.; Li, C.-J.; Jiang, H. Copper-catalyzed oxidative C(sp3)–H functionalization for facile synthesis of 1,2,4-triazoles and 1,3,5-triazines from amidines. Organic Letters, 2015, 17(12), pp. 2894-2897. DOI: https://doi.org/10.1021/acs.orglett.5b00995
• 6. Castanedo, G. M.; Seng, P. S.; Blaquiere, N.; Trapp, S.; Staben, S. T. Rapid synthesis of 1,3,5-substituted 1,2,4-triazoles from carboxylic acids, amidines, and hydrazines. The Journal of Organic Chemistry, 2011, 76(4), pp. 1177-1179. DOI: https://doi.org/10.1021/jo1023393
• 7. Vidavalur, S.; Nakka, M.; Tadikonda, R.; Rayavarapu, S.; Sarakula, P. A Simple and efficient synthesis of 3,4,5-trisubstituted/n-fused 1,2,4-triazoles via ceric ammonium nitrate catalyzed oxidative cyclization of amidrazones with aldehydes using polyethylene glycol as a recyclable reaction medium. Synthesis, 2014, 47(04), pp. 517-525. DOI: https://doi.org/10.1055/s-0034-1378909
• 8. Minozzi, C.; Caron, A.; Grenier-Petel, J.; Santandrea, J.; Collins, S. Heteroleptic copper(I)-based complexes for photocatalysis: combinatorial assembly, discovery, and optimization. Angewandte Chemie International Edition, 2018, 57(19), pp. 5477-5481. DOI: 10.1002/anie.201800144
• 9. Arnold, F. Directed evolution: bringing new chemistry to life. Angewandte Chemie International Edition, 2017, 57(16), pp. 4143-4148. DOI: 10.1002/anie.201708408
• 10. Klimešová, V.; Zahajská, L.; Waisser, K.; Kaustová, J.; Möllmann, U. Synthesis and antimycobacterial activity of 1,2,4-triazole 3-benzylsulfanyl derivatives. Il Farmaco, 2004, 59(4), pp. 279-288. DOI: 10.1016/j.farmac.2004.01.006
• 11. Kapro ´n, B.; Łuszczki, J.J.; Płazi ´nska, A.; Siwek, A.; Karcz, T.; Grybo´s, A.; Nowak, G.; Makuch-Kocka, A.; Walczak, K.; Langner, E. Development of the 1,2,4-triazole-based anticonvulsant drug candidates acting on the voltage-gated sodium channels. Insights from in-vivo, in-vitro, and in-silico studies. Eur. J. Pharm. Sci., 2019, 129, pp. 42–57. https://doi.org/10.1016/j.ejps.2018.12.018
• 12. Timur, ˙I.; Kocyigit, Ü.M.; Dastan, T.; Sandal, S.; Ceribası, A.O.; Taslimi, P.; Gulcin, ˙I.; Koparir, M.; Karatepe, M.; Çiftçi, M.J. In vitro cytotoxic and in vivo antitumoral activities of some aminomethyl derivatives of 2,4-dihydro-3H-1,2,4-triazole-3-thiones—Evaluation of their acetylcholinesterase and carbonic anhydrase enzymes inhibition profiles. Biochem. Mol. Toxicol, 2019, 33, pp. 22239–22250 https://doi.org/10.1002/jbt.22239
• 13. Mishra, C.B.; Mongre, R.K.; Kumari, S.; Jeong, D.K.; Tiwari, M. Novel Triazole-Piperazine Hybrid Molecules Induce Apoptosis via Activation of the Mitochondrial Pathway and Exhibit Antitumor Efficacy in Osteosarcoma Xenograft Nude Mice Model. ACS Chem. Biol, 2017, 17, pp. 753–768. https://doi.org/10.1021/acschembio.6b01007
• 14. Mermer, A.; Demirbaş, N.; Şirin, Y.; Uslu, H.; Özdemir, Z.; Demirbaş, A. Conventional and microwave prompted synthesis, antioxidant, anticholinesterase activity screening and molecular docking studies of new quinolone-triazole hybrids. Bioorganic Chemistry, 2018, 78, pp. 236-248. DOI: 10.1016/j.bioorg.2018.03.017