Bulletin of the Korean Chemical Society

  • 제24권5호
  • /
  • Pages.638-640
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  • 2003
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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Chemoselective N-Nitrosation of Secondary Amines under Mild and Heterogeneous Conditions

  • 발행 : 2003.05.20
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참고문헌

  1. Williams, D. L. H. Supplement F2: The Chemistry of Amino, Nitroso, Nitro and Related Groups; John Wiley & Sons Ltd.: 1996; pp 665-682.
  2. Keefer, L. K.; Williams, D. L. H. Methodsin Nitric Oxide Reseach; John Wiley & Sons Ltd.: 1996; pp 509-519.
  3. Furniss, B. S.; Hannaford, A. J.; Smith, P. W. G.; Tatchell, A.R. Vogels Text Book of Practical Organic Chemistry, 4th Ed.;Longman: London and New York, 1986.
  4. Sheriner, R. L.; Reynold, T. L.; Fuson, C.; Curtin, D. Y.; Morrill, T. C. TheSystematic Identification of Organic Compounds, 6th Ed.; JohnWiley and Sons: 1980; pp 220-223.
  5. Castedo, L.; Riguera, R.; Vezquez, M. P. J. Chem. Soc. Chem. Commun. 1983, 301.
  6. Fanning, J. C.; Keefer, L. K.; Larry, K. J. Chem. Soc. Chem.Commun. 1987, 955.
  7. Nakajima, M.; Warner, J. C.; Anselme, J. P. Tetrahedron Lett.1984, 25, 2619. https://doi.org/10.1016/S0040-4039(01)81245-4
  8. Chang, S. K.; Hrrington, G. W.; Rothstein, M.; Shergalis, W. A.;Swern, D.; Vohra, S. K. Cancer Res. 1979, 39, 3871.
  9. Makhova, N. N.; Karpov, G. A.; Mikhailyuk, A. N.; Bova, A. E.;Khmel´nitskii, L. I.; Novikov, S. S. Izv. Akad. Nauk. SSSR. Ser.Khim. 1978, 1, 226.
  10. Zolfigol, M. A. Synth. Commun. 1999, 29, 905. https://doi.org/10.1080/00397919908086051
  11. Zolfigol, M. A.; Ghaemi, E.; Madrakian, E.; Kiany-Borazjani, M. Synth.Commun. 2000, 30, 2057. https://doi.org/10.1080/00397910008087255
  12. Zolfigol, M. A.; Shirini, F.; Ghorbani Choghamarani, A.; Taqian-Nasab, A.; Keypour, H.;Salehzadeh, S. J. Chem. Research(S) 2000, 420
  13. Zolfigol, M. A.; Nematollahi, D.; Mallakpour, S. E. Synth. Commun. 1999, 29, 2277. https://doi.org/10.1080/00397919908086229
  14. Zolfigol, M. A.; Mallakpour, S. E.; Synth. Commun. 1999, 29, 4061. https://doi.org/10.1080/00397919908085927
  15. Zolfigol, M. A.; Kiany- Borazjani, M.; Sadeghi, M. M.; Mohammadpoor-Baltork, I.; Memarian, H. R. Synth. Commun. 2000, 30, 551. https://doi.org/10.1080/00397910008087352
  16. Zolfigol, M. A. Synth. Commun. 2000, 30, 1593. https://doi.org/10.1080/00397910008087194
  17. Zolfigol, M. A.; Ghaemi, E.; Madrakian, E. Synth. Commun. 2000, 30, 1689. https://doi.org/10.1080/00397910008087210
  18. Zolfigol, M. A.; Mallakpour, S. E.; Madrakian, E.; Ghaemi, E. Indian J. Chem. 2000, 39B, 308.
  19. Zolfigol, M. A.; Kiany-Borazjani, M.; Sadeghi, M. M.; Memarian, H. R.; Mohammadpoor-Baltork, I. J. Chem. Research(S) 2000, 167.
  20. Zolfigol, M. A.; Kiany- Borazjani, M.; Sadeghi, M. M.; Memarian, H. R.; Mohammadpoor- Baltork, I. Synth. Commun. 2000, 30, 2945. https://doi.org/10.1080/00397910008087444
  21. Zolfigol, M. A.; Kiany-Borazjani, M.; Mallakpour, S. E.; Nassr-Isfahani, H. Synth. Commun. 2000, 30, 2573. https://doi.org/10.1080/00397910008087422
  22. Zolfigol, M. A.; Kiany-Borazjani, M.; Sadeghi, M. M.; Mohammadpoor-Baltork, I.; Memarian, H. R. Synth. Commun. 2000, 30, 3919. https://doi.org/10.1080/00397910008086949
  23. Barton, S. D.; Ollis, W. D. Comprehensive Organic Chemistry;Pergamon Press: 1968; Vol. 2, pp 363-370.
  24. Turnbull, K. J. Heterocycl. Chem. 1985, 22, 965. https://doi.org/10.1002/jhet.5570220406
  25. Keypour, H.; Pritchard, R. G.; Parish, R. V. Transition Met.Chem. 1998, 23, 609. https://doi.org/10.1023/A:1006988704602
  26. Keypour, H.; Pritchard, R. G.; Parish, R. V. Transition Met. Chem. 1998, 23, 121. https://doi.org/10.1023/A:1006982723501
  27. Keypour, H.; Salehzadeh, S. Transition Met. Chem. 2000, 25, 205. https://doi.org/10.1023/A:1007017400893
  28. Keypour, H.; Salehzadeh, S.; Pritchard, R. G.; Parish, R. V. Inorg. Chem. 2000, 39, 5787. https://doi.org/10.1021/ic000511m
  29. Ellison, M. K.; Schulz, C. E.; Scheidt, W. R. Inorg. Chem. 2000,39, 5102. https://doi.org/10.1021/ic000789e
  30. Richter-Addo, G. B. Acc. Chem. Res. 1999, 32, 529. https://doi.org/10.1021/ar970351r

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