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Iodine-Catalyzed Synthesis of Spiroorthcarbonates under Neutral Conditions

  • Rahimizadeh, Mohammad (Department of Chemistry, School of Sciences, Ferdowsi University of Mashhad) ;
  • Bakavoli, Mehd (Department of Chemistry, School of Sciences, Ferdowsi University of Mashhad) ;
  • Shiri, Ali (Department of Chemistry, School of Sciences, Ferdowsi University of Mashhad) ;
  • Eshghi, Hossein (Department of Chemistry, School of Sciences, Ferdowsi University of Mashhad)
  • Published : 2009.08.20

Abstract

Keywords

References

  1. Endo, T.; Bailey, W. J. Polym. Sci., Polym. Chem. Ed. 1976, 14, 1735 https://doi.org/10.1002/pol.1976.170140713
  2. Takata, T.; Endo, T. Prog. Polym. Sci. 1993, 18, 839 https://doi.org/10.1016/0079-6700(93)90019-9
  3. Rokicki, G. Prog. Polym. Sci. 2000, 25, 259 https://doi.org/10.1016/S0079-6700(00)00006-X
  4. Sakai, S.; Kiyohara, Y.; Itoh, K.; Ishii, Y. J. Org. Chem. 1970, 35, 2347 https://doi.org/10.1021/jo00832a053
  5. Sakai, S.; Kobayashi, Y.; Itoh, K.; Ishii, Y. J. Org. Chem. 1971, 36, 1176 https://doi.org/10.1021/jo00808a002
  6. Endo, T.; Okawara, M. Synthesis 1984, 837
  7. Stansbury, J. W. J. Dent. Res. 1992, 71, 1408 https://doi.org/10.1177/00220345920710070901
  8. Mues, P.; Buysch, H. Synthesis 1990, 249
  9. Sanda, F.; Takata, T.; Endo, T. Macromolecules 1993, 26, 737 https://doi.org/10.1021/ma00056a027
  10. Banerjee, A. K.; Vera, W.; Mora, H.; Laya, M. S.; Bedoya, L.; Cabrera, E. V. J. Sci. Ind. Res. 2006, 65, 299.
  11. Bakavoli, M.; Shiri, A.; Ebrahimpour, Z.; Rahimizadeh, M. Chin. Chem. Lett. 2008, 19, 1403. https://doi.org/10.1016/j.cclet.2007.04.020
  12. Rahimizadeh, M.; Shiri, A.; Bakavoli, M. Chin. Chem. Lett. 2007, 18, 689 https://doi.org/10.1016/j.cclet.2007.04.020
  13. Rahimizadeh, M.; Bakavoli, M.; Shiri, A.; Eshghi, H.; Saberi, S. J. Chem. Res. 2008, 704 https://doi.org/10.1002/pola.1990.080281228
  14. Sugiyama, J.; Yokozawa, T.; Endo, T. J. Polym. Sci., Part A: Polym. Chem. 1990, 28, 3529 https://doi.org/10.1002/pola.1990.080281228
  15. Sakai, S.; Kobayashi, Y.; Ishii, Y. J. Chem. Soc., Chem. Commun. 1970, 4, 235

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