Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
권호 표지
DOI QR코드

DOI QR Code

An Efficient Synthetic Route for New 1,3,4-Oxadiazoles Having Sulphonamido Pharmacophore

  • Jagrut, Vasant B. (Dnyanopasak College) ;
  • Netankar, Prashant D. (Dept. of Chemistry, Dr. Babasaheb Ambedkar Marathwada University) ;
  • Jawale, Dhanaji V. (Dept. of Chemistry, Dr. Babasaheb Ambedkar Marathwada University) ;
  • Mane, Ramrao A. (Dept. of Chemistry, Dr. Babasaheb Ambedkar Marathwada University) ;
  • Jadhav, Wamanrao N. (Dnyanopasak College)
  • Published : 2009.11.20
Download PDF
⟨ Previous Next ⟩

Abstract

Keywords

References

  1. Long, H. P.; Bliss, A. B. J. Am. Med. Asso. 1937, 32, 108
  2. The pharmacological Basis of Therapeutics, 8th Ed.; Mandell, G. L.; Sande, M. A.; Gilman, A. G.; Rall, T. W.; Nies, A. S.; Taylor, P., Eds.; Pergamon Press: New York
  3. Boyd, A. E. Diabetes 1988, 37, 847 https://doi.org/10.2337/diabetes.37.7.847
  4. Singh, B. N. Drugs 1987, 34, 311. https://doi.org/10.2165/00003495-198734030-00002
  5. Hohnloser, S. H.; Woosley, R. L.; Engl, N. J. Med. Chem. 1994, 331, 31 https://doi.org/10.1021/jm00315a037
  6. Lorsen. J. Med. Chem. 1967, 10, 462. https://doi.org/10.1021/jm00315a037
  7. Dunjan, K. W. et al. J. Pharmacol. Exp. Ther. 1968, 164, 290
  8. Decker, O. D.; Gohnson, W. S. Anal. Methods Pestic, Plant Growth Rev. 1976, 8, 433
  9. Claudiu, T.; Supuran, A. S.; Francesco, M. L.; Menabuoni, M. J. Eur. J. Med. Chem. 1999, 34, 585 https://doi.org/10.1016/j.bmc.2005.05.011
  10. Sahin, G.; Palaska, E.; Ekizoglu, M.; Ozalp, M. Farmaco II 2002, 57, 539. https://doi.org/10.1016/j.antiviral.2006.02.007
  11. Bhat, K. S.; Karthikeyan, M. S.; Holla, B. S. Indain J. Chem. 2004, 43B, 1765 https://doi.org/10.1016/j.bmcl.2004.09.072
  12. Gudima, A.; Stingaci, E.; Vlad, L.; Shvets, N.; Kandemirij, F.; Dimoglo, A.; Reynoids, R. Bioorg. Med. Chem. 2005, 13, 4842 https://doi.org/10.1016/j.farmac.2004.05.007
  13. Tan, T. M. C.; Chen, Y.; Kong, K. H.; Bai, J.; Li, Y.; Hin, S. G.; Ang, T. H.; Lam, Y. Antiviral Res. 2006, 71, 7 https://doi.org/10.1016/S0022-1139(03)00168-4
  14. Almasirad, A.; Tabatabai, S. A.; Faizi, M.; Kebriaceezadeh, A.; Mehrabi, N.; Dalvandi, A.; Shafiee, A. Bioorg. Med. Chem. Lett. 2004, 14, 6057 https://doi.org/10.1016/j.mejo.2005.12.005
  15. Burbuliene, M. M.; Jakubkiene, V.; Mekuskeine, G.; Vdrenaite, E.; Smicius, R.; Vainilavicius, P. Farmaco II 2004, 59, 767 https://doi.org/10.1016/j.farmac.2004.05.007
  16. Zheng, X.; Li, Z.; Wang, Y.; Chem, W.; Huang, Q.; Liu, C.; Song, G. J. Fluorine Chem. 2003, 123, 163 https://doi.org/10.1016/S0022-1139(03)00168-4
  17. Zhan, S.; Ying, -G. X.; Xia, L.; Tao, Y. J. Microelectronics 2006, 37, 714 https://doi.org/10.1016/j.mejo.2005.12.005
  18. Partyka, R. A.; Crenshaw, R. R. 1, 3, 4-Oxadiazole Amides, U. S. Patent 4001-238, 1977. https://doi.org/10.1081/SCC-100103993
  19. Vardan, S.; Mookherjee, S.; Eich, R. Chn. Pharm. Therp. 1983, 34(3), 290 https://doi.org/10.1080/07328309108543919
  20. Theime, P. C.; Eranke, A.; Denke, D.; Lehmann, H. D.; Gries, J. Ger. Offen. 1981, 29. https://doi.org/10.3390/10091161
  21. Schlecker, R.; Thieme, P. C. Tetrahedron 1988, 44, 3289 https://doi.org/10.1080/00397919008053105
  22. Hirao, I. Nippon Kagaku. Zasshi. 1967, 88, 574. https://doi.org/10.1080/00397910008087340
  23. Ogata, M.; Atobe, H.; Kushi-da, H.; Yamamoto, K. J. Antibiot. 1971, 24, 443 https://doi.org/10.1021/jm00111a021
  24. Tandon, V. K.; Chhor, R. B. Synth. Commun. 2001, 31, 1727 https://doi.org/10.1081/SCC-100103993
  25. Mansour, E. M. E.; Kassem, A. A.; Abass, T. M.; Eltoukhy, A. A.; Nassr, M. A. M. J. Carbohydr. Chem. 1991, 10, 429 https://doi.org/10.1080/07328309108543919
  26. Sharba, A. H. K.; Al-Bayati, R. H.; Aouad, M.; Rezki, N. Molecules 2005, 10, 1161 https://doi.org/10.1016/S0040-4039(99)00382-2
  27. Al-Talib, M.; Tastoush, H.; Odeh, N. Synth. Commun. 1990, 20, 1811 https://doi.org/10.1080/00397919008053105
  28. Liras, S.; Allen, M. P.; Segelstein, B. E. Synth. Commun. 2000, 30, 437 https://doi.org/10.1081/SCC-120024002
  29. Tully, W. R.; Gardner, C. R.; Gillespie, R. J.; Westwood, R. J. Med. Chem. 1991, 34, 2060 https://doi.org/10.1021/jm00111a021
  30. Brown, B. J.; Clemens, I. R.; Neesom, J. K. Synlett. 2000, 131
  31. Brain, C. T.; Brunton, S. A. Synlett. 2001, 382
  32. Brain, C. T.; Paul, J. M.; Loong, Y.; Oakley, P. J. Tetrahedron Lett. 1999, 40, 3275 https://doi.org/10.1016/S0040-4039(99)00382-2
  33. Ladva, K.; Patel, P.; Upadhyay, P.; Parekh, H. Ind. J. Chem. 1996, 35B, 3427
  34. QLai, L.Y.; Ferguson, Y.; Jones, M. Synth. Commun. 2003, 33, 3427 https://doi.org/10.1081/SCC-120024002

Cited by

  1. -Arylsulfonamide Formation through Directly Using Nitroarenes as Nitrogen Sources vol.80, pp.7, 2015, https://doi.org/10.1021/acs.joc.5b00130
  2. para-Aminobenzoic Acid-A Substrate of Immense Significance vol.17, pp.6, 2020, https://doi.org/10.2174/1570193x16666190828201234