Facile synthesis, characterization, and antimicrobial studies of some disubstituted 1,2,3-triazoles with sulfonamide functionality

References

• Thomas, K. D.; Adhikari, A. V.; Shetty, N. S. Eur. J. Med. Chem. 2010, 45, 3803–3810.
   PubMed Web of Science ®Google Scholar
• Petrova, K. T.; Potewar, T. M.; Silva, P. C. D.; Barros, M. T. R. C.; Ciric, A.; Sokovic, M.; Ferreira, I. C. F. R. Carbohydrate Research 2015, 417, 66–71.
   PubMed Web of Science ®Google Scholar
• Vatmurge, N. S.; Hazra, B. G.; Pore, V. S.; Shirazi, F.; Chavan, P. S.; Deshpande, M. V. Bioorg. Med. Chem. Lett. 2008, 18, 2043–2047.
   PubMed Web of Science ®Google Scholar
• Kaushik, C. P.; Kumar, K.; Singh, S. K.; Singh, D.; Saini, S. Arab. J. Chem. 2016, 9, 865–871.
   Web of Science ®Google Scholar
• Kaushik, C. P.; Kumar, K.; Lal, K.; Singh, S. K. Chem. Biol. Interface 2014, 4, 341–350.
   Google Scholar
• Kaushik, C. P.; Kumar, K.; Singh, D.; Singh, S. K.; Jindal, D. K.; Luxmi, R. Synth. Commun. 2015, 45, 1977–1985.
   Web of Science ®Google Scholar
• Wang, X. L.; Wan, K.; Zhou, C. H. Eur. J. Chem. 2010, 45, 4631–4639.
   Web of Science ®Google Scholar
• Ouahrouch, A.; Taourirte, M.; Engels, J. W.; Benjelloun, S.; Lazrek, H. B. Molecules 2014, 19, 3638–3653.
   PubMed Web of Science ®Google Scholar
• Buckle, D. R.; Rockell, C. J. M.; Smith, H.; Spicer, B. A. J. Med. Chem. 1986, 29, 2262–2267.
   PubMed Web of Science ®Google Scholar
• Singh, P.; Raj, R.; Kumar, V.; Mahajan, M. P.; Bedi, P. M.; Kaur, T.; Saxena, A. K. Eur. J. Med. Chem. 2012, 47, 594–600.
   PubMed Web of Science ®Google Scholar
• Alvarez, S.; San, F.; Aquaro, S.; De, C.; Perno, C. F.; Karlsson, A.; Balzarini, J.; Camarasa, M. J. J. Med. Chem. 1994, 37, 4185–4194.
   PubMed Web of Science ®Google Scholar
• Santos, J. A. D.; Corrales, R. C. N. R.; Pavan, F. R.; Leite, C. Q. F.; Dias, R. M. D. P.; Silva, A. D. D. Mediterr. J. Chem. 2012, 1, 282–288.
   Google Scholar
• Bakunov, S. A.; Bakunova, S. M.; Wenzler, T.; Ghebru, M.; Werbovetz, K. A.; Brun, R.; Tidwell, R. R. J. Med. Chem. 2010, 53, 254–272.
   PubMed Web of Science ®Google Scholar
• Vasilevsky, S. F.; Baranov, D. S.; Govdi, A. I.; Sorokina, I. V.; Tolstikova, T. G.; Tolstikov, G. A.; Alabugin, I. V. Arkivoc 2014, (V), 145–157.
   Web of Science ®Google Scholar
• Karakurt, A.; Ayetmir, M. D.; Stables, J. P.; Ozalp, M.; Kaynak, F. B.; Ozbey, S.; Dalkara, S. Arch. Pharm. Chem. Life Sci. 2006, 339, 513–520.
   PubMed Web of Science ®Google Scholar
• Horne, W. S.; Yadav, M. K.; Stout, D. C.; Ghadiri, M. R. J. Am. Chem. Soc. 2004, 126, 15366–15367.
   PubMed Web of Science ®Google Scholar
• Kwok, S. W.; Fotsing, J. R.; Fraser, R. J.; Rodionov, V. O.; Fokin, V. V. Org. Lett. 2010, 12, 4217–4219.
   PubMed Web of Science ®Google Scholar
• Kolb, H. C.; Finn, M. G.; Sharpless, K. B. Angew. Chem. 2001, 40, 2004–2021.
   Google Scholar
• Tornфe, C. W.; Christensen, C.; Meldal, C. M. J. Org. Chem. 2002, 67, 3057–3064.
   PubMed Web of Science ®Google Scholar
• Huisgen, R.; Szeimies, G.; Moebius, L. Chem. Ber. 1967, 100, 2494–2507.
   Google Scholar
• Rivara, M.; Patel, M. K.; Amori, L.; Zuliani, V. Bioorg. Med. Chem. Lett. 2012, 22, 6401–6404.
   PubMed Web of Science ®Google Scholar
• Su, X.; Shuai, Y.; Guo, Z.; Feng, Y. Molecules 2013, 18, 4599–4612.
   PubMed Web of Science ®Google Scholar
• Palomo, J. M. Org. biol. Chem. 2012, 10, 9309–9318.
   PubMed Web of Science ®Google Scholar
• Arseneault, M.; Wafer, C.; Morin, J. F. Molecules 2015, 20, 9263–9294.
   PubMed Web of Science ®Google Scholar
• Li, H.; Aneja, R.; Chaiken, I. Molecules 2013, 18, 9797–9817.
   PubMed Web of Science ®Google Scholar
• Fuaad, A. A. H. A.; Azmi, F.; Skwarczynski, M.; Toth, I. Molecules 2013, 18, 13148–13174.
   PubMed Web of Science ®Google Scholar
• Gallardo, H.; Ely, F.; Bortoluzzi, A. J.; Conte, G. Liq. Cryst. 2005, 32, 667–671.
   Web of Science ®Google Scholar
• Kaushik, C. P.; Lal, K.; Kumar, A.; Kumar, S. Med. Chem. Res. 2014, 23, 2995–3004.
   Web of Science ®Google Scholar
• Kaushik, C. P.; Kumar, K.; Lal, K.; Narasimhan, B.; Kumar, A. Monatsh. Chem. 2016, 147, 817–828.
   Web of Science ®Google Scholar
• Cappucino, J. G.; Sherman, N. Microbiology: A Laboratory Manual 4th ed.; Addison Wesley, Longman Inc: Harlow, 1999; p. 263.
   Google Scholar
• Trott, O.; Olson, A. J. J. Comput. Chem. 2010, 31, 455–461.
   PubMed Web of Science ®Google Scholar
• Kumar, A.; Kumar, S.; Jain, S.; Kumar, P.; Goyal, R. Med. Chem. Res. 2013, 22, 5431–5441.
   Web of Science ®Google Scholar
• Marvin Sketch 5.10.1 ChemAxon Ltd. 1998–2012. http://www.chemaxon.com.
   Google Scholar
• Pettersen, E. F.; Goddard, T. D.; Huang, C. C.; Couch, G. S.; Greenblatt, D. M.; Meng, E. C.; Ferrin, T. E. J. Comput. Chem. 2004, 25, 1605–1612.
   PubMed Web of Science ®Google Scholar
• Dunbrack, R. L. Curr. Opin. Struct. Biol. 2002, 12, 431–440.
   PubMed Web of Science ®Google Scholar
• Wang, J.; Wang, W.; Kollman, P. A.; Case, D. J. Mol. Graph. Model. 2006, 25, 247–260.
   PubMed Web of Science ®Google Scholar
• AutoDock Tools (version 1.5.6 rc2), Stefano Forte. Molecular Graphics Laboratory, Department of Molecular Biology, The Scripps Research Institute, 1999–2010. http://mgltools.scripps.edu
   Google Scholar
• DeLano, W. L. PyMOL(TM) Molecular Graphics System, Version 1.7.5.0. Copyright (c) Schrodinger, LLC.
   Google Scholar
• Discovery Studio Visualizer v4.0.100.13345. Accelrys Software Inc., 2005–2013.
   Google Scholar