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Comparative Liquid Chromatographic Enantiomer Resolution on Two Chiral Stationary Phases Derived from Amylose Tris(3,5-dimethylphenylcarbamate)

  • Published : 2005.07.20

Abstract

Keywords

References

  1. Yashima, E. J. Chromatogr. A 2001, 906, 105 https://doi.org/10.1016/S0021-9673(00)00501-X
  2. Okamoto, Y.; Yashima, E. Angew. Chem. Int. Ed. 1998, 37, 1020 https://doi.org/10.1002/(SICI)1521-3773(19980504)37:8<1020::AID-ANIE1020>3.0.CO;2-5
  3. Refer to Application Guide for Chiral HPLC Selection, 3rd Ed.; Daicel Chemical Industries, Ltd
  4. Franco, P.; Senso, A.; Oliveros, L.; Minguillión, C. J. Chromatogr. A 2001, 906, 155 https://doi.org/10.1016/S0021-9673(00)00531-8
  5. Okamoto, Y.; Aburatani, R.; Miura, S.; Hatada, K. J. Liq. Chromatogr. 1987, 10, 1613 https://doi.org/10.1080/01483918708066791
  6. Kimata, K.; Tsuboi, R.; Hosoya, K.; Tanaka, N. Anal. Methods Instrum. 1993, 1, 23
  7. Yashima, E.; Fukaya, H.; Okamoto, Y. J. Chromatogr. A 1994, 677, 11 https://doi.org/10.1016/0021-9673(94)80539-3
  8. Oliveros, L.; López, P.; Minguillón, C.; Franco, P. J. Liq. Chromatogr. 1995, 18, 1521 https://doi.org/10.1080/10826079508009292
  9. Minguillon, C.; Franco, P.; Oliveros, L.; Lopez, P. J. Chromatogr. A 1996, 728, 407 https://doi.org/10.1016/0021-9673(95)01123-4
  10. Enomoto, N.; Furukawa, S.; Ogasawara, Y.; Akano, H.; Kawamura, Y.; Yashima, E.; Okamoto, Y. Anal. Chem. 1996, 68, 2798 https://doi.org/10.1021/ac960002v
  11. Franco, P.; Minguillón, C.; Oliveros, L. J. Chromatogr. A 1998, 793, 239 https://doi.org/10.1016/S0021-9673(97)00935-7
  12. Franco, P.; Senso, A.; Minguillón, C.; Oliveros, L. J. Chromatogr. A 1998, 796, 265 https://doi.org/10.1016/S0021-9673(97)01004-2
  13. Kim, B.-H.; Lee, W. J. Liq. Chromatogr. & Rel. Tech. 1999, 22, 523 https://doi.org/10.1081/JLC-100101677
  14. Li, Y. H.; Baek, C.-S.; Jo, B. W.; Lee, W. Bull. Kor. Chem. Soc. 2005, 26, 998 https://doi.org/10.5012/bkcs.2005.26.6.998
  15. Rizzi, A. M. J. Chromatogr. 1989, 478, 71
  16. Miyazawa, T.; Shindo, Y.; Yamada, T.; Kuwata, S. Anal. Lett. 1993, 26, 457 https://doi.org/10.1080/00032719308016811
  17. Spondlin, Ch.; Kusters, E. Chromatographia 1994, 38, 325 https://doi.org/10.1007/BF02269775
  18. Miyazawa, T.; Shindo, Y.; Yamada, T. Chromatographia 2004, 60, 419 https://doi.org/10.1365/s10337-004-0388-4
  19. Bodansky, M.; Bodansky, A. The Practice of Peptide Synthesis; Springer: New York, 1984

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