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Tungstate Sulfuric Acid (TSA)/NaNO2 as a Novel Heterogeneous System for Rapid Deoximation

  • Published : 2005.09.20

Abstract

Keywords

References

  1. Zolfigol, M. A. Tetrahedron 2001, 57, 9509-9511 https://doi.org/10.1016/S0040-4020(01)00960-7
  2. Olah, G. A.; Molhotra, R.; Narang, S. C. J. Org. Chem. 1987, 43, 4628
  3. Zolfigol, M. A.; Shirin, F.; Ghorbani Choghamarani, A.; Mohammadpoor-Baltork, I. Green Chem. 2002, 4, 562 https://doi.org/10.1039/b208328k
  4. Zolfigol, M. A.; Bamoniri, A. Synlett 2002, 1621
  5. Mirjalili, B. F.; Zolfigol, M. A.; Bamoniri, A. J. Korean Chem. Soc. 2001, 45, 546
  6. Mirjalili, B. F.; Zolfigol, M. A.; Bamoniri, A. Molecules 2002, 7, 751 https://doi.org/10.3390/71000751
  7. Mirjalili, B. F.; Zolfigol, M. A.; Bamoniri, A.; Zarei, A. Bull. Korean Chem. Soc. 2003, 24, 400 https://doi.org/10.5012/bkcs.2003.24.3.400
  8. Mirjalili, B. F.; Zolfigol, M. A.; Bamoniri, A.; Zaghaghi, Z. J. Chem. Research(S) 2003, 273
  9. Mirjalili, B. F.; Zolfigol, M. A.; Bamoniri, A.; Zaghaghi, Z.; Hazar, A. Acta Chem. Slov. 2003, 50, 563
  10. Shirini, F.; Zolfigol, M. A.; Mohammadi, K. Bull. Korean Chem. Soc. 2004, 25, 325 https://doi.org/10.5012/bkcs.2004.25.2.325
  11. Harmer, M. A.; Sun, Q. Appl. Catal. A: General 2001, 221, 45 https://doi.org/10.1016/S0926-860X(01)00794-3
  12. Heydari, A.; Larijani, H.; Emami, J.; Karami, B. Tetrahedron Lett. 2000, 41, 2471 https://doi.org/10.1016/S0040-4039(00)00182-9
  13. Asgarian Damavandi, J.; Zolfigol, M. A.; Karami, B. Synth. Commun. 2001, 31, 129
  14. Hamal, S., Santosh, K. M.; Chhabilal, G. Ind. J. Chem. 1996, 35B, 1116
  15. Mohammadpoor-Baltork, I.; Pouranshirani, S. Synth. Commun. 1996, 26(1), 1 https://doi.org/10.1080/00397919608003856
  16. Bandgar, B. P.; Shaikh, S. I.; Iyer, S. Synth. Commun. 1996, 26(6), 1163 https://doi.org/10.1080/00397919608003724
  17. Bose, S. D. ; Srinivas, P. Synth. Commun. 1997, 27(22), 3835 https://doi.org/10.1080/00397919708005905
  18. Barhate, N. B.; Gajare, A. S.; Wakharkar, R. D.; Sadalai, A. Tetrahedron Lett. 1997, 38(4), 653 https://doi.org/10.1016/S0040-4039(96)02384-2
  19. Verma, R. S.; Meshram, H. M. Tetrahedron Lett. 1997, 38(31), 5427 https://doi.org/10.1016/S0040-4039(97)01213-6
  20. Chaudhari, S. S.; Akamanchi, K. G. Tetrahedron Lett. 1998, 39(20), 3209 https://doi.org/10.1016/S0040-4039(98)00392-X
  21. Hajipour, A. R.; Mahboubghah, N. J. Chem. Res. (S) 1998, 123
  22. Verma, R. S.; Dahia, R.; Saini, R. K. Tetrahedron Lett. 1997, 38, 8819 https://doi.org/10.1016/S0040-4039(97)10521-4
  23. House, H. O. Modern Synthetic Reactions, 2nd ed.; Benjamin, W. A., California, 1972; p 275
  24. Sam, D. J.; Simmons, H. F. J. Am. Chem. Soc. 1972, 94, 4024 https://doi.org/10.1021/ja00766a069
  25. Hershberg, E. B. J. Org. Chem. 1984, 13, 542 https://doi.org/10.1021/jo01162a011
  26. Drabowiez, J. Synthesis 1980, 125
  27. Rao, C. G.; Radhakrishna, A. S.; Singh, R. B.; Bhatnagar, S. P. Synthesis 1983, 808
  28. Bandgar, B. P.; Kunde, M. L. B.; Thote, J. L. Synth. Commun. 1997, 27, 1149 https://doi.org/10.1080/00397919708003350
  29. Butler, R. N.; Morris, G. J.; Odonohue, A. M. J. Chem. Res. (S) 1981, 61
  30. Shim, S. B.; Kim, K.; Kim, Y. H. Tetrahedron. Lett. 1987, 28, 645 https://doi.org/10.1016/S0040-4039(00)95802-7
  31. Salmon, M.; Miranda, R.; Angeles, E. Synth. Commun. 1986, 16, 1827 https://doi.org/10.1080/00397918608057207
  32. Moriarty, R. M.; Prakash, O.; Vavilikolanu, R. Synth. Commun. 1986, 16, 1247 https://doi.org/10.1080/00397918608056372
  33. Vankar, P.; Rathore, R.; Chandrasekaran, S. J. Org. Chem. 1986, 51, 3063 https://doi.org/10.1021/jo00365a042
  34. Chidambaram, N.; Satyanarayana, K.; Chandrasekaran, S. Synth. Commun. 1989, 19, 1724
  35. Mona, D.; Cramman, P.; Spranzo, G.; Tagliapietra, P.; Manam, P. Synth. Commun. 1986, 16, 803 https://doi.org/10.1080/00397918608059661
  36. Dictionary of Organic Compounds, 6th ed.; Chapman and Hall: London, 1982

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