참고문헌
- Chiral Separation Techniques: A Practical Approach; Subramanian, G., Ed.; Wiley-VCH: Weinheim, 2001
- Aboul- Enein, H. Y.; Ali, I. Chiral Separations by Liquid Chromatography and Related Technologies; Marcel Dekker: New York, 2003
- Hyun, M. H. J. Sep. Sci. 2003, 26, 242 https://doi.org/10.1002/jssc.200390030
- Hyun, M. H. Bull. Kor. Chem. Soc. 2005, 26, 1153 https://doi.org/10.5012/bkcs.2005.26.8.1153
- Hyun, M. H. J. Sep. Sci. 2006, 29, 750 https://doi.org/10.1002/jssc.200500431
- Shinbo, T.; Yamaguchi, T.; Nishimura, K.; Sugiura, M. J. Chromatogr. 1987, 405, 145 https://doi.org/10.1016/S0021-9673(01)81756-8
- Shinbo, T.; Yamaguchi, T.; Yanagishita, H.; Kitamoto, D.; Sakaki, K.; Sugiura, M. J. Chromatogr. 1992, 625, 101 https://doi.org/10.1016/0021-9673(92)85191-U
- Hyun, M. H.; Han, S. C.; Lipshutz, B. H.; Shin, Y.-J.; Welch, C. J. J. Chromatogr. A 2001, 910, 359 https://doi.org/10.1016/S0021-9673(00)01230-9
- Hyun, M. H.; Han, S. C.; Lipshutz, B. H.; Shin, Y.-J.; Welch, C. J. J. Chromatogr. A 2002, 959, 7
- Hyun, M. H.; Han, S. C. J. Biochem. Biophys. Methods 2002, 54, 235 https://doi.org/10.1016/S0165-022X(02)00117-3
- Hyun, M. H.; Min, H. J.; Cho, Y. J. J. Chromatogr. A 2003, 996, 233 https://doi.org/10.1016/S0021-9673(03)00540-5
- Hyun, M. H.; Tan, G.; Cho, Y. J. Biomed. Chromatogr. 2005, 19, 208 https://doi.org/10.1002/bmc.437
- Hyun, M. H.; Jin, J. S.; Lee, W. J. Chromatogr. A 1998, 822, 155 https://doi.org/10.1016/S0021-9673(98)00606-2
- Hyun, M. H.; Cho, Y. J.; Jin, J. S. J. Sep. Sci. 2002, 25, 648 https://doi.org/10.1002/1615-9314(20020701)25:10/11<648::AID-JSSC648>3.0.CO;2-D
- Hyun, M. H.; Cho, Y. J.; Kim, J. A.; Jin, J. S. J. Liq. Chromatogr. Rel. Technol. 2003, 26, 1083 https://doi.org/10.1081/JLC-120020095
- Berkecz, R.; Sztojkov-Ivanov, A.; Ilisz, I.; Forro, E.; Fulop, F.; Hyun, M. H.; Peter, A. J. Chromatogr. A 2006, 1125, 138 https://doi.org/10.1016/j.chroma.2006.06.064
- Hyun, M. H.; Min, H. J.; Cho, Y. J. Bull. Kor. Chem. Soc. 2003, 24, 911 https://doi.org/10.5012/bkcs.2003.24.7.911
- 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
- Hyun, M. H.; Jin, J. S.; Lee, W. Bull. Kor. Chem. Soc. 1998, 19, 819
- Hyun, M. H.; Han, S. C.; Jin, J. S.; Lee, W. Chromatographia 2000, 52, 473 https://doi.org/10.1007/BF02535722
- Hyun, M. H.; Han, S. C.; Cho, Y. J.; Jin, J. S.; Lee, W. Biomed. Chromatogr. 2002, 16, 356 https://doi.org/10.1002/bmc.164
- Hyun, M. H.; Kim, Y. H.; Cho, Y. J. Bull. Kor. Chem. Soc. 2004, 25, 400 https://doi.org/10.5012/bkcs.2004.25.3.400
- Hyun, M. H.; Cho, Y. J. J. Sep. Sci. 2005, 28, 31 https://doi.org/10.1002/jssc.200401919
- Wasserman, H. H.; Matsuyama, H.; Robinson, R. P. Tetrahedron 2002, 58, 7177 https://doi.org/10.1016/S0040-4020(02)00731-7
-
Juaristi, E.; Soloshonok, V. A. Enantioselective Synthesis of
$\beta$ -Amino Acids, 2nd ed.; Wiley- VCH: New York, 2005 - Pirkle, W. H.; Koscho, M. E. J. Chromatogr. A 1999, 840, 151 https://doi.org/10.1016/S0021-9673(99)00222-8
피인용 문헌
- High-performance liquid chromatographic enantioseparation of isoxazoline-fused 2-aminocyclopentanecarboxylic acids on a chiral ligand-exchange stationary phase vol.36, pp.8, 2013, https://doi.org/10.1002/jssc.201201061
- Application of crown ethers as stationary phase in the chromatographic methods vol.75, pp.1-2, 2013, https://doi.org/10.1007/s10847-012-0158-0
- Comparison of the Separation Performances of Cinchona Alkaloid-Based Zwitterionic Stationary Phases in the Enantioseparation of β2- and β3-Amino Acids vol.20, pp.1, 2014, https://doi.org/10.3390/molecules20010070
- LC Enantioseparation of β-Amino Acids on a Crown Ether-Based Stationary Phase vol.68, pp.S1, 2008, https://doi.org/10.1365/s10337-007-0498-x
- -homoamino acids vol.31, pp.21, 2008, https://doi.org/10.1002/jssc.200800388
- -homoamino acids using crown ether-based chiral stationary phase vol.32, pp.7, 2009, https://doi.org/10.1002/jssc.200800561
- The role of π-acidic and π-basic chiral stationary phases in the high-performance liquid chromatographic enantioseparation of unusual β-amino acids vol.21, pp.3, 2009, https://doi.org/10.1002/chir.20542
- -homoamino acids vol.21, pp.9, 2009, https://doi.org/10.1002/chir.20670
- Liquid Chromatographic Resolution of N-(3,5-Dinitrobenzoyl)-α-amino Acids on a New Chiral Stationary Phase: the First Liquid Chromatographic Utilization of a Double-Ureide Pocket for the Recogn vol.28, pp.11, 2006, https://doi.org/10.5012/bkcs.2007.28.11.1980
- Synthesis of New Chiral Crown Ethers Incorporating Two Different Chiral Units and 'Matched/Mismatched' Effect of the Two Chiral Units on the Chiral Recognition vol.28, pp.12, 2006, https://doi.org/10.5012/bkcs.2007.28.12.2531
- An NMR Chiral Solvating Agent for the Chiral Recognition of the Two Enantiomers of N-(3,5-Dinitrobenzoyl)-α-amino Acids vol.28, pp.8, 2007, https://doi.org/10.5012/bkcs.2007.28.8.1419
- Preparation of a new chiral acridino-18-crown-6 ether-based stationary phase for enantioseparation of racemic protonated primary aralkyl amines vol.64, pp.6, 2006, https://doi.org/10.1016/j.tet.2007.09.056
- Liquid chromatographic resolution of β-amino acids on CSPs based on optically active (3,3'-diphenyl-1,1'-binaphthyl)-20-crown-6 vol.619, pp.1, 2008, https://doi.org/10.1016/j.aca.2008.03.052
- High-performance liquid chromatographic enantioseparation of monoterpene-based 2-amino carboxylic acids on macrocyclic glycopeptide-based phases vol.1217, pp.44, 2006, https://doi.org/10.1016/j.chroma.2010.08.079