DOI QR코드

DOI QR Code

Amylose Tris(3,5-dimethylphenylcarbamate)-Coated Zirconia as a Chiral Stationary Phase for Micro HPLC


Abstract

Keywords

References

  1. Francotte, E. In Chiral Separations: Applications and Technology;Ahuja, S., Ed.; American Chemical Society: Washington, 1997;Chapter 5.
  2. Dingenen, J. In A Practical Approach to Chiral Separations byLiquid Chromatography; Subramanian, G., Ed.; VCH: New York,1994; Chapter 6.
  3. Okamoto, Y.; Kawashima, M.; Yamamoto, K.; Hatada, K. Chem.Lett. 1984, 739.
  4. Okamoto, Y.; Kawashima, M.; Hatada, K. J. Am. Chem. Soc.1984, 106, 5357. https://doi.org/10.1021/ja00330a057
  5. Okamoto, O.; Kawashima, M.; Hatada, K. J. Chromatogr. 1986,363, 173. https://doi.org/10.1016/S0021-9673(01)83736-5
  6. Okamoto, O.; 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
  7. Okamoto, Y.; Kaida, Y.; Aburatani, R.; Hatada, K. In Chiral Separationsby Liquid Chromatography; Ahuja, S., Ed.; ACS SymposiumSeries 471; American Chemical Society: Washington, DC,1991; pp 101-113.
  8. Kirkland, J. J.; van Straten, M. A.; Claessans, H. A. J. Chromatogr.1995, 691, 3. https://doi.org/10.1016/0021-9673(94)00631-I
  9. Nawrocki, J.; Dunlap, C. J.; Carr, P. W.; Blackwell, J. A. Biotechnol.Prog. 1994, 10, 561. https://doi.org/10.1021/bp00030a001
  10. Jackson, P. T.; Carr, P. W. Chemtech. Oct. 29, 1998.
  11. Castells, C. B.; Carr, P. W. Anal. Chem. 1999, 71, 3013. https://doi.org/10.1021/ac990021f
  12. Park, J. H.; Ryu, J. K.; Park, J. K.; McNeff, C. V.; Carr, P. W.Chromatographia 2001, 53, 405. https://doi.org/10.1007/BF02491075
  13. Park, S. Y.; Park, J. K.; Park, J. H.; McNeff, C. V.; Carr, P. W.Microchem. J. 2001, 70, 179. https://doi.org/10.1016/S0026-265X(01)00129-1
  14. Horvath, C. G.; Preiss, B. A.; Lipsky, S. R. Anal. Chem. 1967, 39,1422. https://doi.org/10.1021/ac60256a003
  15. Scott, R. P. W.; Kucera, P. J. Chromatogr. 1976, 125, 251. https://doi.org/10.1016/S0021-9673(00)93823-8
  16. Ishii, D. In Introduction to Microscale High-Performance LiquidChromatography; Ishii, D., Ed.; VCH: Weinheim, 1988; Chapter 1.
  17. Okamoto, Y.; Aburatani, R.; Fukumoto, T.; Hatada, K. Chem. Lett.1987, 1857.
  18. Koller, H.; Rimbock, K. H.; Mannschreck, A. J. Chromatogr. A1983, 282, 89. https://doi.org/10.1016/S0021-9673(00)91594-2

Cited by

  1. )-γ-Lactones with a Combination of Lipase-Catalyzed Resolution and Mitsunobu Reaction vol.39, pp.9, 2009, https://doi.org/10.1080/00397910802546177
  2. Zirconia-Based Stationary Phases for Chiral Separation: Mini Review vol.45, pp.1, 2012, https://doi.org/10.1080/00032719.2011.582553
  3. Aluminum chloride-mediated kinetic resolution of racemic ?-substituted-?-lactones vol.16, pp.5, 2004, https://doi.org/10.1002/chir.20036
  4. Conventional Chiralpak ID vs. Capillary Chiralpak ID-3 Amylose Tris-(3-Chlorophenylcarbamate)-Based Chiral Stationary Phase Columns for the Enantioselective HPLC Separation of Pharmaceutical Racemates vol.26, pp.11, 2014, https://doi.org/10.1002/chir.22390
  5. 9-O-(Phenylcarbamoyl)quinine-bonded Carbon-Clad Zirconia for Chiral Separation of Racemic 2,4-Dinitrophenyl Amino Acids in RPLC vol.27, pp.4, 2002, https://doi.org/10.5012/bkcs.2006.27.4.589