References
- Chu, C. K.; Ma, T. W.; Shanmuganathan, K.; Wang, C. G.; Xiang, Y. J.; Pai, S. B.; Yao, G. Q.; Sommadossi, J.-P.; Cheng, Y.-C. Antimicrob. Agents Chemother. 1995, 39, 979. https://doi.org/10.1128/AAC.39.4.979
- Schinazi, R. F.; Gosselin, G.; Faraj, A.; Korba, B. E.; Liotta, D. C.; Chu, C. K.; Mathe, C.; Imbach, J.-L.; Sommadossi, J.-P. Antimicrob. Agents Chemother. 1994, 38, 2172. https://doi.org/10.1128/AAC.38.9.2172
- Gosselin, G.; Schinazi, R. F.; Sommadossi, J.-P.; Mathe, C.; Bergogne, M.-C.; Aubertin, A.-M.; Kirn, A.; Imbach, J.-L. Antimicrob. Agents Chemother. 1994, 38, 1292. https://doi.org/10.1128/AAC.38.6.1292
- Chang, C.-N.; Skalski, V.; Zhou, J. H.; Cheng, Y.-C. J. Biol. Chem. 1992, 267, 22414.
- Schinazi, R. F.; McMillan, A.; Cannon, D.; Mathis, R.; Lloyd, R. M.; Peck, A.; Sommadossi, J.-P.; St. Clair, M.; Wilson, J.; Furman, P. A.; Painter, G.; Choi, W. B.; Liotta, D. C. Antimicrob. Agents Chemother. 1992, 36, 2413. https://doi.org/10.1128/AAC.36.11.2413
- Spadari, S.; Maga, G.; Focher, F.; Ciarrocchi, G.; Manservigi, R.; Arcamone, F.; Capobianco, M.; Carcuro, A.; Colonna, F.; Iotti, S.; Garbesi, A. J. Med. Chem. 1992, 35, 4214. https://doi.org/10.1021/jm00100a029
- Goodchild, J. Bioconjugate Chem. 1990, 1, 16.
- Uhlmann, E.; Peyman, A. Chem. Rev. 1990, 90, 543. https://doi.org/10.1021/cr00102a001
- Beaucage, S. L.; Iyer, R. P. Tetrahedron 1993, 49, 6123. https://doi.org/10.1016/S0040-4020(01)87958-8
- Schafer, A. In The Carbohydrates: Chemistry and Biochemistry, 2nd ed.; Pigman, W.; Horton, D., Eds.; Academic Press: New York, 1972; Vol. IA, pp 85-86.
- Frush, H. L.; Isbell, H. S. Methods Carbohydr. Chem. 1962, 1, 127.
- Ko, S. Y.; Sharpless, K. B. Science 1983, 220, 949. https://doi.org/10.1126/science.220.4600.949
- Gonzalez, F. S.; Baer, H. H. Carbohydr. Res. 1990, 202, 33. https://doi.org/10.1016/0008-6215(90)84069-7
- Root, R. L.; Durrwachter, J. R.; Wong, C.-H. J. Am. Chem. Soc. 1985, 107, 2997. https://doi.org/10.1021/ja00296a041
- Kim, K. S.; Cho, I. H.; Ahn, Y. H.; Park, J. I. J. Chem. Soc., Perkin Trans. 1 1995, 1783.
- Harmuth, C. K.; VanNeieuwenhze, M. S.; Sharpless, K. B. Chem. Rev. 1994, 94, 2483. https://doi.org/10.1021/cr00032a009
- Wolfrom, M. L. J. Am. Chem. Soc. 1930, 52, 2464. https://doi.org/10.1021/ja01369a045
- Araki, C.; Hirase, S. Bull. Chem. Soc. Jpn. 1953, 26, 463. https://doi.org/10.1246/bcsj.26.463
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