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A Short Synthesis of a Novel Nucleoside Analog of Fosfomycin


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참고문헌

  1. Glamkowski, E. J.; Gal, G.; Purick, R.; Davidson, A. J.; Sletzinger, M. J. Org. Chem. 1970, 35, 3510. https://doi.org/10.1021/jo00835a070
  2. Springs, B.; Haake, P. J. Org. Chem. 1976, 41, 1165. https://doi.org/10.1021/jo00869a017
  3. Giordano, C.; Castaldi, G. J. Org. Chem. 1989, 54, 1470. https://doi.org/10.1021/jo00267a050
  4. Bandini, E.; Martelli, G.; Spunta, G.; Panunzio, M. Tetrahedron: Asymmetry 1995, 6, 2127. https://doi.org/10.1016/0957-4166(95)00281-S
  5. Kitamura, M.; Tokunaga, M.; Noyori, R. J. Am. Chem. Soc. 1995, 117, 2931. https://doi.org/10.1021/ja00115a030
  6. Iorga, B.; Eymery, F.; Savignac, P. Synthesis 1999, 2, 207.
  7. Kobayashi, Y.; William, A. D.; Tokoro, Y. J. Org. Chem. 2001, 66, 7903. https://doi.org/10.1021/jo010701u
  8. Hendlin, D.; Stapley, E. O.; Jackson, M.; Wallick, H.; Miller, A. K.; Wolf, F. J.; Miller, T. W.; Chaiet, L.; Kahan, F. M.; Foltz, E. L.; Woodruff, H. B.; Mata, J. M.; Hernandez, S.; Mochales, S. Science 1969, 166, 122. https://doi.org/10.1126/science.166.3901.122
  9. Inouye, S.; Niizato, T.; Komiya, L.; Yuda, Y.; Yamada, Y. Pharm. Dyn. 1982, 5, 941. https://doi.org/10.1248/bpb1978.5.941
  10. Inokawa, S.; Kawata, Y.; Yamamota, K.; Kawamoto, H.; Yamamoto, H.; Takagi, K.; Yamashita, M. Carbohydr. Res. 1981, 88, 341. https://doi.org/10.1016/S0008-6215(00)85549-4
  11. Inokawa, S.; Yamamoto, H. Phosphorus Sulfur 1983, 16, 79. https://doi.org/10.1080/03086648308077754
  12. McEldoon, W. L.; Wiemer, D. F. Tetrahedron 1996, 52, 11695. https://doi.org/10.1016/0040-4020(96)00684-9
  13. Jung, K. Y.; Hohl, R. J.; Wiemer, A. J.; Wiemer, D. F. Bioorg. & Med. Chem. 2000, 8, 2501. https://doi.org/10.1016/S0968-0896(00)00183-8
  14. Kozlowski, J. K.; Rath, N. P.; Spilling, C. D. Tetrahedron 1995, 51, 6385. https://doi.org/10.1016/0040-4020(95)00308-U
  15. Wroblewski, A. E.; Piotrowska, D. G. Tetrahedron: Asymmetry 1999, 10, 2037. https://doi.org/10.1016/S0957-4166(99)00206-2
  16. This mandelate ester was crystallized from CHCI₃very slowly(about 2 months)

피인용 문헌

  1. 5′,6′-Nucleoside Phosphonate Analogues Architecture: Synthesis and Comparative Evaluation towards Metabolic Enzymes vol.6, pp.6, 2011, https://doi.org/10.1002/cmdc.201100068
  2. A Short Synthesis of a Novel Nucleoside Analogue of Fosfomycin. vol.34, pp.16, 2003, https://doi.org/10.1002/chin.200316219
  3. Synthesis of Oxazolidinone Phosphonate Derivatives, Part I vol.25, pp.9, 2004, https://doi.org/10.5012/bkcs.2004.25.9.1326
  4. New analogues of fosfomycin—synthesis of diethyl (1R,2R)- and (1S,2R)-1,2-epoxy-3-hydroxypropylphosphonates vol.18, pp.4, 2007, https://doi.org/10.1016/j.tetasy.2007.02.006