DOI QR코드

DOI QR Code

Green and Metal-free Catalytic Oxidation of Urazoles into Triazolinediones by Guanidinium Nitrate and Catalytic Amounts of Silica Sulfuric Acid

  • Received : 2010.04.23
  • Accepted : 2010.06.07
  • Published : 2010.08.20

Abstract

Keywords

References

  1. Min, B. K.; Friend, C. M. Chem. Rev. 2007, 127, 2709.
  2. Ghorbani-Choghamarani, A.; Zolfigol, M. A.; Ayazi-Nasrabadi, R. J. Braz. Chem. Soc. 2010, 21, 33. https://doi.org/10.1590/S0103-50532010000100006
  3. Gao, Y.; Lam, Y. Adv. Synth. Catal. 2008, 350, 2937. https://doi.org/10.1002/adsc.200800500
  4. Zolfigol, M. A.; Bagherzadeh, M.; Niknam, K.; Shirini, F.; Mohammadpoor-Baltork, I.; Ghorbani-Choghamarani, A.; Baghbanzadeh, M. J. Iran. Chem. Soc. 2006, 3, 73. https://doi.org/10.1007/BF03245793
  5. Abraham, S.; Rajan, P. K.; Sreekumar, K. Polym. J. 1997, 29, 12. https://doi.org/10.1295/polymj.29.12
  6. Shirini, F.; Zolfigol, M. A.; Salehi, P.; Abedini, M. Curr. Org. Chem. 2008, 12, 183. https://doi.org/10.2174/138527208783497475
  7. Wei, Y.; Lemal, D. M. Org. Lett. 2004, 6, 3837. https://doi.org/10.1021/ol040051r
  8. Vougioukalakis, G. C.; Roubelakis, M. M.; Alberti, M. N.; Orfanopoulos, M. Chem. Eur. J. 2008, 14, 9697. https://doi.org/10.1002/chem.200800920
  9. Syrgiannis, Z.; Koutsianopoulos, F.; Muir, K. W.; Elemes, Y. Tetrahedron Lett. 2009, 50, 277. https://doi.org/10.1016/j.tetlet.2008.10.150
  10. Menard-Moyon, C.; Gross, M.; Bernard, M.; Turek, P.; Doris, E.; Mioskowski, C. Eur. J. Org. Chem. 2007, 4817.
  11. Zolfigol, M. A.; Ghorbani-Choghamarani, A.; Shahamirian, M.; Safaiee, M.; Mohammadpoor-Baltork, I.; Mallakpour, S. E.; Abdollahi-Alibeik, M. Tetrahedron Lett. 2005, 46, 5581. https://doi.org/10.1016/j.tetlet.2005.06.031
  12. Cookson, R. C.; Stevens, I. D. R.; Watts, C. T. Chem. Commun. 1966, 744.
  13. Christoforou, A.; Nicolaou, G.; Elemes, Y. Tetrahedron Lett. 2006, 47, 9211. https://doi.org/10.1016/j.tetlet.2006.10.134
  14. Ghorbani-Choghamarani, A.; Goudarziafshar, H.; Nikoorazm, M.; Yousefi, S. Lett. Org. Chem. 2009, 6, 535. https://doi.org/10.2174/157017809789869500
  15. Ghorbani-Choghamarani, A.; Rezaei, S. J. Chin. Chem. Soc. 2009, 56, 251. https://doi.org/10.1002/jccs.200900036
  16. Habibi, D.; Zolfigol, M. A.; Safaiee, M.; Shamsian, A.; Ghorbani-Choghamarani, A. Catal. Commun. 2009, 10, 1257. https://doi.org/10.1016/j.catcom.2008.12.066
  17. Amani, K.; Zolfigol, M. A.; Ghorbani-Choghamarani, A.; Hajjami, M. Monatsh. Chem. 2009, 140, 65. https://doi.org/10.1007/s00706-008-0015-4
  18. Zolfigol, M. A.; Amani, K.; Hajjami, M.; Ghorbani-Choghamarani, A. Monatsh. Chem. 2008, 139, 895. https://doi.org/10.1007/s00706-008-0868-6
  19. Zolfigol, M. A.; Amani, K.; Ghorbani-Choghamarani, A.; Hajjami, M.; Ayazi-Nasrabadi, R.; Jafari, S. Catal. Commun. 2008, 9, 1739. https://doi.org/10.1016/j.catcom.2008.01.029
  20. Ghorbani-Choghamarani, A.; Chenani, Z.; Mallakpour, S. Synthetic Commun. 2009, 39, 4264. https://doi.org/10.1080/00397910902898619
  21. Ghorbani-Choghamarani, A.; Goudarziafshar, H.; Nikoorazm, M.; Yousefi, S. Can. J. Chem. 2009, 87, 1144.
  22. Ghorbani-Choghamarani, A.; Nikoorazm, M.; Goudarziafshar, H.; Tahmasbi, H. Bull. Korean. Chem. Soc. 2009, 30, 1388. https://doi.org/10.5012/bkcs.2009.30.6.1388
  23. Ghorbani-Choghamarani, A.; Shiri, L.; Zeinivand, J. Bull. Korean Chem. Soc. 2008, 29, 2496. https://doi.org/10.5012/bkcs.2008.29.12.2496
  24. Zolfigol, M. A.; Bagherzadeh, M.; Mallakpour, S.; Chehardoli, G.; Kolvari, E.; Ghorbani-Choghamarani, A.; Koukabi, N. Catal. Commun. 2007, 8, 256. https://doi.org/10.1016/j.catcom.2006.04.006
  25. Zolfigol, M. A.; Ghorbani-Vaghei, R.; Mallakpour, S.; Chehardoli, G.; Ghorbani-Choghamarani, A.; Hosain-Yazdi, A. Synthesis 2006, 1631.
  26. Zolfigol, M. A.; Chehardoli, G.; Ghaemi, E.; Madrakian, E.; Zare,R.; Azadbakht, T.; Niknam, K.; Mallakpour, S. Monatsh. Chem.2008, 139, 261. https://doi.org/10.1007/s00706-007-0785-0
  27. Ghorbani-Choghamarani, A.; Hajjami, M.; Goudarziafshar, H.; Nikoorazm, M.; Mallakpour, S.; Sadeghizadeh, F.; Azadi, G. Monatsh. Chem. 2009, 140, 607. https://doi.org/10.1007/s00706-008-0100-8

Cited by

  1. from Hydrogen Peroxide/Acids/Iodide Potassium or Sodium Systems vol.32, pp.12, 2011, https://doi.org/10.5012/bkcs.2011.32.12.4366
  2. Triazolinediones as Highly Enabling Synthetic Tools vol.116, pp.6, 2016, https://doi.org/10.1021/acs.chemrev.5b00599
  3. ChemInform Abstract: Green and Metal‐Free Catalytic Oxidation of Urazoles into Triazolinediones by Guanidinium Nitrate and Catalytic Amounts of Silica Sulfuric Acid. vol.42, pp.1, 2010, https://doi.org/10.1002/chin.201101118