DOI QR코드

DOI QR Code

Chromatographic Separation of Enantiomers of Chiral Amines or Amino Alcohols as 9-Anthraldimine Derivatives Using Polysaccharide-Derived Chiral Columns

  • Received : 2011.04.21
  • Accepted : 2011.06.09
  • Published : 2011.07.20

Abstract

Keywords

References

  1. Huang, H.; Jin, J. Y.; Hong, J. H.; Lee, W.; Han, H.-K.; Kang, J. S. J. Liq. Chrom. & Rel. Tech. 2011, 34, 209. https://doi.org/10.1080/10826076.2011.546162
  2. Greene T. W.; Wuts, P. G. M. Protective Groups in Organic Synthesis, 3rd ed.; John Wiley & Sons. Inc.: New York, 1999.
  3. Duchateau, A. L. L.; Guns, J. J.; Kubben, R. G. R.; van Tilburg, A. F. P. J. Chromatogr. A 1994, 664, 169. https://doi.org/10.1016/0021-9673(94)87004-7
  4. Application Guide for Chiral HPLC selection, 4th ed.; Daicel Chemical Industries, Ltd.
  5. Zhang, T.; Kientzy, C.; Franco, P.; Ohnishi, A.; Kagamihara, Y.; Kurosawa, H. J. Chromatogr. A 2005, 1075, 65. https://doi.org/10.1016/j.chroma.2005.03.116
  6. Zhang, T.; Nguyen, D.; Franco, P.; Murakami, T.; Ohnishi, A.; Kurosawa, H. Anal. Chim. Acta 2006, 557, 221. https://doi.org/10.1016/j.aca.2005.10.017
  7. Jin, J. Y.; Lee, W.; Park, J. H.; Ryoo, J. J. J. Liq. Chrom. & Rel. Tech. 2007, 30, 1. https://doi.org/10.1080/10826070601034170
  8. Zhang, T.; Nguyen, D.; Franco, P.; Isobe, Y.; Michishita, T.; Murakami, T. J. Pharm. Biomed. Anal. 2008, 46, 882. https://doi.org/10.1016/j.jpba.2007.06.008
  9. Thunberg, L.; Hashemi, J.; Andersson, S. J. Chromatogr. B 2008, 875, 72. https://doi.org/10.1016/j.jchromb.2008.07.044
  10. Zhang, T.; Nguyen, D.; Franco, P. J. Chromatogr. A 2008, 1191, 214. https://doi.org/10.1016/j.chroma.2007.12.026
  11. Jin, J. Y.; Bae, S. K.; Lee, W. Chirality 2009, 21, 871. https://doi.org/10.1002/chir.20680
  12. Yashima, E.; Fukaya, H.; Okamoto, Y. J. Chromatogr. A 1994, 677, 11. https://doi.org/10.1016/0021-9673(94)80539-3

Cited by

  1. A convenient and validated enantiomer separation of chiral aliphatic amines as nitrobenzoxadiazole derivatives on polysaccharide-derived chiral stationary phases under simultaneous ultraviolet and fluorescence detection vol.28, pp.12, 2016, https://doi.org/10.1002/chir.22659
  2. Liquid Chromatographic Enantiomeric Separation of Chiral Aliphatic Amines Using 2-Hydroxynaphthaldehyde as a Derivatizing Agent on Polysaccharide-Derived Chiral Stationary Phases vol.81, pp.9, 2018, https://doi.org/10.1007/s10337-018-3560-y
  3. An Exploration of Induced Supramolecular Chirality Through Association of Chiral Ammonium Ions and Tartrates with the Achiral Host Cucurbit[7]uril vol.58, pp.3-4, 2018, https://doi.org/10.1002/ijch.201700112
  4. -phthaldialdehyde/mercaptoethanol derivatives on polysaccharide-based chiral stationary phases vol.31, pp.3, 2019, https://doi.org/10.1002/chir.23047
  5. Efficient preparation of stereopure amphiphilic 1,2‐amino alcohols by using preparative enantioselective HPLC vol.34, pp.2, 2011, https://doi.org/10.1002/chir.23395