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Free Radical Acylation Approach of carbohydrate Derivatives


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References

  1. Brimacombe, J. S. Angew. Chem. Int. Ed. 1969, 6, 401.
  2. Grisebach, H.; Schmid, R. Angew. Chem. Int. Ed. 1972, 11, 159. https://doi.org/10.1002/anie.197201591
  3. Hanessian, S. Acc. Chem. Res. 1979, 12, 159. https://doi.org/10.1021/ar50137a001
  4. Hanessian, S. Total Synthesis of Natural Products: The Chiron Approach; Pergamon Press: Oxford, 1983.
  5. For a review, see: Postema, M. H. D. Tetrahedron 1992, 48, 8545. https://doi.org/10.1016/S0040-4020(01)89435-7
  6. Curran, D. P. Synthesis 1988, 489.
  7. Radicals in Organic Synthesis, Vol 1, Renaud, P.; Sibi, M. P., Eds.; Wiley-VCH: Weinheim, Germany, 2001; Vol. 1.
  8. Giese, B.; Dupuis, J. Angew. Chem. Int. Ed. 1983, 22, 633. https://doi.org/10.1002/anie.198306331
  9. Kita, Y.; Gotanda, K.; Sano, A.; Oka, M.; Murata, K.; Suemura, M.; Matsugi, M. Tetrahedron Lett. 1997, 38, 8345. https://doi.org/10.1016/S0040-4039(97)10259-3
  10. Keck, G.; Yates, J. B. J. Am. Chem. Soc. 1982, 104, 5829. https://doi.org/10.1021/ja00385a066
  11. Keck, G.; Enholm, E. J.; Yates, J. B.; Wiley, M. R. Tetrahedron 1985, 41, 4079. https://doi.org/10.1016/S0040-4020(01)97185-6
  12. Junker, H.-D.; Fessner, W.-D. Tetrahedron Lett. 1998, 39, 269. https://doi.org/10.1016/S0040-4039(97)10498-1
  13. Hart, D. J.; Seely, F. L. J. Am. Chem. Soc. 1988, 110, 1631. https://doi.org/10.1021/ja00213a051
  14. Gupta, V.; Kahne, D. Tetrahedron Lett. 1993, 34, 591. https://doi.org/10.1016/S0040-4039(00)61627-1
  15. Kim, S.; Lee, I. Y.; Yoon, J.-Y.; Oh, D. H. J. Am. Chem. Soc. 1996, 118, 5138. https://doi.org/10.1021/ja9600993
  16. Kim, S.; Yoon, J.-Y.; Lee, I. Y. Synlett 1997, 475.
  17. Kim, S.; Yoon, J.-Y. J. Am. Chem. Soc. 1997, 119, 5982. https://doi.org/10.1021/ja9710316
  18. Feuer, H.; Vincent, B. F.; Bartlett, R. S. J. Org. Chem. 1965, 30, 2877. https://doi.org/10.1021/jo01020a001
  19. Feuer, H.; Braunstein, D. M. J. Org. Chem. 1969, 34, 1817. https://doi.org/10.1021/jo01258a062
  20. Itsuno, S.; Tanaka, K.; Ito, K. Chem. Lett. 1986, 1133.
  21. Korth, H.-G.; Sustmann, R. J. Org. Chem. 1988, 53, 4364. https://doi.org/10.1021/jo00253a032
  22. Koch, A.; Lamberth, C.; Wetterich, F.; Giese, B. J. Org. Chem. 1993, 58, 1083. https://doi.org/10.1021/jo00057a020
  23. Togo, H.; He, W.; Waki, Y.; Yokohama, M. Synlett 1998, 700
  24. Giese, B.; Dupuis, J.; Leising, M.; Nix, M.; Lindner, H. J. Carbohydr. Res. 1987, 171, 329. https://doi.org/10.1016/S0008-6215(00)90896-6
  25. Richards, G. N. J. Chem. Soc. 1954, 4511. https://doi.org/10.1039/jr9540004511
  26. Richards, G. N.; Wiggins, L. F.; Wise, W. S. J. Chem. Soc. 1956, 496. https://doi.org/10.1039/jr9560000496
  27. Wiggins, L. F. Methods in Carbohydr. Chem. 1963, 2, 188.
  28. Furstner, A.; Weidmann, H. J. Org. Chem. 1989, 54, 2307. https://doi.org/10.1021/jo00271a012

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