Bulletin of the Korean Chemical Society

  • 제33권10호
  • /
  • Pages.3481-3484
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  • 2012
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  • 0253-2964(pISSN)
  • /
  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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Comparative Studies on Enantiomer Resolution of α-Amino Acids and Their Esters Using (18-Crown-6)-tetracarboxylic acid as a Chiral Crown Ether Selector by NMR Spectroscopy and High-Performance Liquid Chromatography

  • 투고 : 2012.06.26
  • 심사 : 2012.07.13
  • 발행 : 2012.10.20
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참고문헌

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  2. Hyun, M. H.; Jin, J. S.; Koo, H. J.; Lee, W. J. Chromatogr. A 1999, 837, 75. https://doi.org/10.1016/S0021-9673(99)00100-4
  3. Hyun, M. H.; Koo, H. J.; Jin, J. S.; Lee, W. J. Liq. Chrom. & Rel. Technol. 2000, 23, 2669. https://doi.org/10.1081/JLC-100101825
  4. Lee, W.; Jin, J. Y.; Baek, C.-S. Microchem. J. 2005, 80, 213. https://doi.org/10.1016/j.microc.2004.07.010
  5. Jin, J. Y.; Lee, W.; Hyun, M. H. J. Liq. Chrom. & Rel. Technol. 2006, 29, 841. https://doi.org/10.1080/10826070500531102
  6. Jin, J. Y.; Lee, W. Chirality 2007, 19, 120. https://doi.org/10.1002/chir.20354
  7. Machida, Y.; Nishi, H.; Nakamura, K.; Nakai, H.; Sato, T. J. Chromatogr. A 1998, 805, 85. https://doi.org/10.1016/S0021-9673(98)00013-2
  8. Machida, Y.; Nishi, H.; Nakamura, K. J. Chromatogr. A 1998, 810, 33. https://doi.org/10.1016/S0021-9673(98)00207-6
  9. Hyun, M. H. Bull. Korean Chem. Soc. 2005, 26, 1153. https://doi.org/10.5012/bkcs.2005.26.8.1153
  10. Hyun, M. H. J. Sep. Sci. 2006, 29, 750. https://doi.org/10.1002/jssc.200500431
  11. Bang, E.; Jung, J.-W.; Lee, W.; Lee, D. W.; Lee, W. J. Chem. Soc. Perkin Trans. 2 2001, 9, 1685.
  12. Lee, W.; Bang, E.; Lee, W. Chromatographia 2003, 57, 457. https://doi.org/10.1007/BF02492541
  13. Lee, W.; Bang, E.; Baek, C.-S.; Lee, W. Magn. Reson. Chem. 2004, 42, 389. https://doi.org/10.1002/mrc.1353
  14. Wenzel, T. J.; Thurston, J. E. Tetrahedron Lett. 2000, 41, 3769. https://doi.org/10.1016/S0040-4039(00)00499-8
  15. Wenzel, T. J.; Thurston, J. E. J. Org. Chem. 2000, 65, 1243. https://doi.org/10.1021/jo9913154
  16. Machida, Y.; Kagawa, M.; Nishi, H. J. Pharm. Biomed. Anal. 2003, 30, 1929. https://doi.org/10.1016/S0731-7085(02)00537-X
  17. Park, H.-J.; Choi, Y.; Lee, W.; Kim, K.-R. Electrophoresis 2004, 25, 2755. https://doi.org/10.1002/elps.200405963
  18. Lee, W.; La, S.; Choi, Y.; Kim, K.-R. Bull. Korean Chem. Soc. 2003, 24, 1232. https://doi.org/10.5012/bkcs.2003.24.8.1232
  19. Wenzel, T. J.; Wilcox, J. D. Chirality 2003, 15, 256. https://doi.org/10.1002/chir.10190

피인용 문헌

  1. Discrimination of α-Amino Acids Using Green Tea Flavonoid (−)-Epigallocatechin Gallate as a Chiral Solvating Agent vol.78, pp.6, 2013, https://doi.org/10.1021/jo3025016
  2. Deracemization of Racemic Amino Acids Using (R)- and (S)-Alanine Racemase Chiral Analogues as Chiral Converters vol.35, pp.7, 2014, https://doi.org/10.5012/bkcs.2014.35.7.2186
  3. Chiral separation using chiral crown ethers as chiral selectors in chirotechnology pp.2093-6214, 2018, https://doi.org/10.1007/s40005-017-0348-2
  4. Enantiodiscrimination Using a Chiral Crown Ether as a Chiral Solvating Agent Using NMR Spectroscopy vol.14, pp.5, 2012, https://doi.org/10.1177/1934578x19849191
  5. Effective enantiomeric identification of aromatic amines by tyrosine-modified pillar[5]arenes as chiral NMR solvating agents vol.8, pp.15, 2012, https://doi.org/10.1039/d1qo00525a