1,2,4-Triazole-3-Thiones: Greener, One-Pot, Ionic Liquid Mediated Synthesis and Antifungal Activity

References

• J. Jampilek, “Heterocycles in Medicinal Chemistry,” Molecules 24, no. 21 (2019): 3839.
   PubMed Web of Science ®Google Scholar
• P. Martins, J. Jesus, S. Santos, L. R. Raposo, C. Roma-Rodrigues, P. V. Baptista, and A. R. Fernandes, “Heterocyclic Anticancer Compounds: recent Advances and the Paradigm Shift towards the Use of Nanomedicine’s Toolbox,” Molecules 20, no. 9 (2015): 16852–91.
   PubMed Web of Science ®Google Scholar
• L. Zhou, H. M. Lokman, and T. Xiao, “Synthesis of N-Containing Heterocyclic Compounds Using Visible-Light Photoredox Catalysis,” Chemical Record 16, no. 1 (2016): 319–34.
   PubMed Web of Science ®Google Scholar
• R. Aggarwal and G. Sumran, “An Insight on Medicinal Attributes of 1,2,4-Triazoles,” European Journal of Medicinal Chemistry 20, (2020): 112652.
   Google Scholar
• E. Bonandi, M. S. Christodoulou, G. Fumagalli, D. Perdicchia, G. Rastelli, and D. Passarella, “The 1,2,3-Triazole Ring as a Bioisostere in Medicinal Chemistry,” Drug Discovery Today 22, no. 10 (2017): 1572–81.
   PubMed Web of Science ®Google Scholar
• T. Taj, R. Kamble, A. Dorababu, and G. Y. Meti, “Synthesis of Novel 1,2,4-Triazole Derivatives as Antimicrobial Agents via the Japp-Klingemann Reaction: Investigation of Antimicrobial Activities,” Journal of Chemistry 2013 (2013): 909706.
   Web of Science ®Google Scholar
• L. Yanga and X. P. Bao, “Synthesis of Novel 1,2,4-Triazole Derivatives Containing the Quinazolinylpiperidinyl Moiety and N-(Substituted Phenyl)Acetamide Group as Efficient Bactericides against the Phytopathogenic Bacterium Xanthomonas oryzae pv. Oryzae,” RSC Advances 7 (2017): 34005–11.
   Web of Science ®Google Scholar
• S. Mallakpour and Z. Rafiee, “Ionic Liquids as Environmentally Friendly Solvents in Macromolecules Chemistry and Technology, Part I,” Journal of Polymers and the Environment 19 (2011): 447–84.
   Web of Science ®Google Scholar
• A. Abdulrhman, A. B. Muhsinah, Y. I. Asiri, A. A. Jaber, Y. N. Mabkhot, M. Y. Alfaifi, I. E. Serag Eldin, M. H. Mahnashi, and M. Z. Hassan, “Arylhydrazono/Aryldiazenyl Pyrazoles: green One-Pot Solvent-Free Synthesis and Anticancer Evaluation,” Letters in Organic Chemistry 17, no. 10 (2020): 772–78.
   Web of Science ®Google Scholar
• M. Z. Hassan, S. A. Khan, and M. Amir, “Design, Synthesis and Evaluation of N-(Substituted Benzothiazol-2-yl)Amides as Anticonvulsant and Neuroprotective,” European Journal of Medicinal Chemistry 58 (2012): 206–13.
   PubMed Web of Science ®Google Scholar
• A. A. Al Sheikh, D. Khan, A. Naqvi, F. F. Al-Blewi, N. Rezki, M. R. Aouad, and M. Hagar, “Design, Synthesis, Molecular Modeling, Anticancer Studies, and Density Functional Theory Calculations of 4-(1,2,4-Triazol-3-Ylsulfanylmethyl)-1,2,3-Triazole Derivatives,” ACS Omega 6, no. 1 (2021): 301–16.
   PubMed Web of Science ®Google Scholar
• S. Rostamizadeh, K. Mollahoseini, and S. Moghadasi, “A One-Pot Synthesis of 4,5-Disubstituted-1,2,4-Triazole-3-Thiones on Solid Support under Microwave Irradiation,” Phosphorus, Sulfur, and Silicon and the Related Elements 18, (2006): 1839–45.
   Google Scholar
• S. Yu, X. Chai, Y. Wang, Y. Cao, J. Zhang, Q. Wu, D. Zhang, Y. Jiang, T. Yan, and Q. Sun, “Triazole Derivatives with Improved in Vitro Antifungal Activity over Azole Drugs,” Drug Design, Development and Therapy 8 (2014): 383–90.
   PubMed Web of Science ®Google Scholar
• Y. Wang, K. Xu, G. Bai, L. Huang, Q. Wu, W. Pan, and S. Yu, “Synthesis and Antifungal Activity of Novel Triazole Compounds Containing Piperazine Moiety,” Molecules 19 (2014): 11333–40.
   PubMed Web of Science ®Google Scholar
• B. Luo, D. Li, A. L. Zhang, and J. M. Gao, “Synthesis, Antifungal Activities and Molecular Docking Studies of Benzoxazole and Benzothiazole Derivatives,” Molecules 23 (2018): 2457.
   PubMed Web of Science ®Google Scholar
• E. N. Djuidje, S. Sciabica, R. Buzzi, V. Dissette, J. Balzarini, S. Liekens, E. Serra, E. Andreotti, S. Manfredini, S. Vertuani, et al. “Design, Synthesis and Evaluation of Benzothiazole Derivatives as Multifunctional Agents,” Bioorganic Chemistry 101 (2020): 103960.
   PubMed Web of Science ®Google Scholar
• B. A. Arthington-Skaggs, M. Moltely, D. W. Warnock, and C. J. Morrison, “Comparative Evaluation of Pasco and National Committee for Clinical Laboratory Standards M27-A Broth Microdilution Methods for Antifungal Drug Susceptibility Testing of Yeasts,” Journal of Clinical Microbiology 38 (2000): 2254–60.
   PubMed Web of Science ®Google Scholar
• R. S. Verma, Z. K. Khan, and A. P. Singh, Antifungal Agents: Past, Present and Future Prospects (Lucknow: National Academy of Chemistry and Biology, 1998), 55–128.
   Google Scholar
• T. Y. Hargrove, L. Friggeri, Z. Wawrzak, A. Qi, W. J. Hoekstra, R. J. Schotzinger, J. D. York, F. P. Guengerich, and G. I. Lepesheva, “Structural Analyses of Candida albicans Sterol 14α-Demethylase Complexed with Azole Drugs Address the Molecular Basis of Azole-Mediated Inhibition of Fungal Sterol Biosynthesis,” The Journal of Biological Chemistry 292, no. 16 (2017): 6728–43.
   PubMed Web of Science ®Google Scholar