1 |
Hyun, M. H., J. S. Jin, and W. Lee (1998) A new HPLC chiral stationary phase for the direct resolution of racemic quinolone antibacterials containing a primary amino group. Bull. Kor. Chem. Soc. 19: 819-821.
과학기술학회마을
|
2 |
Hyun, M. H., J. S. Jin, and W. Lee (1998) Liquid chromatographic resolution of racemic amino acids and their derivatives on a new chiral stationary phase based on crown ether. J. Chromatogr. A. 822: 155-161.
DOI
|
3 |
Hyun, M. H., J. S. Jin, and W. Lee (1999) Liquid chromatographic resolution of racemic amines and amino alcohols on a chiral stationary phase derived from crown ether. J. Chromatogr. A. 837: 75-82.
DOI
|
4 |
Hyun, M. H., S. C. Han, J. S. Jin, and W. Lee (2000) Separation of the stereoisomers of racemic fluoroquinolone antibacterial agents on a crown-ether-based chiral HPLC stationary phase. Chromatographia 52: 473-476.
DOI
|
5 |
Hyun, M. H., S. C. Han, Y. J. Cho, J. S. Jin, and W. Lee (2002) Liquid chromatographic resolution of gemifloxacin mesylate on a chiral stationary phase. Biomed. Chromatogr. 16: 356-360.
DOI
|
6 |
Lee, W., C.-S. Baek, and K. Lee (2002) Chromatographic enantiomer separation of diphenylalanine on chiral stationary phases derived from chiral crown ethers. Bull. Kor. Chem. Soc. 23: 1677-1679.
과학기술학회마을
DOI
|
7 |
Lee, W., J. Y. Jin, and C.-S. Baek (2005) Comparison of enantiomer separation on two chiral stationary phases derived from (+)-18-crown-6-2,3,11,12-tetracarboxylic acid of the same chiral selector. Microchem. J. 80: 213-217.
DOI
|
8 |
Jin, J. Y., W. Lee, and M. H. Hyun (2006) Development of the antipode of the covalently-bonded crown ether type chiral stationary phase for the advantage of the reversal of elution order. J. Liq. Chrom. & Rel. Tech. 29: 841-848.
DOI
|
9 |
Machida, Y., H. Nishi, K. Nakamura, H. Nakai, and T. Sato (1998) Enantiomer separation of amino compounds by a novel chiral stationary phase derived from crown ether. J. Chromatogr. A. 805: 85-92.
DOI
|
10 |
Machida, Y., H. Nishi, and K. Nakamura (1998) Nuclear magnetic resonance studies for the chiral recognition of the novel chiral stationary phase derived from 18-crown-6 tetracarboxylic acid. J. Chromatogr. A. 810: 33-41.
DOI
|
11 |
Hyun, M. H., Y. J. Cho, J. A. Kim, and J. S. Jin (2003) Preparation and application of a new modified liquid chromatographic chiral stationary phase based on (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid. J. Chromatogr. A. 984: 163-171.
DOI
|
12 |
Hyun, M. H., H. J. Koo, J. S. Jin, and W. Lee (2000) Liquid chromatographic resolution of racemic compounds containing a primary amino group on a dynamic chiral stationary phase derived from chiral crown ether. J. Liquid Chrom. & Rel. Tech. 23: 2669-2682.
DOI
ScienceOn
|
13 |
Jin, J. Y. and W. Lee (2007) Liquid chromatographic enantiomer resolution of N-hydrazide derivatives of 2-aryloxypropionic acids on a crown ether derived chiral stationary phase. Chirality. 19: 120-123.
DOI
|
14 |
Bang, E., J.-W. Jung, W. Lee, D. W. Lee, and W. Lee (2001) Chiral recognition of (18-crown-6)-tetracarboxylic acid as a chiral selector determined by NMR spectrocropy. J. C. S. Perkin Trans. 2: 1685-1692.
|
15 |
Lee, W., E. Bang, and W. Lee (2003) Chiral resolution of diphenylalanine by high-performance liquid chromatography on a crown-ether-based chiral stationary phase and by NMR spectroscopy. Chromatographia. 57: 457-461.
DOI
ScienceOn
|
16 |
Lee, W., E. Bang, C.-S. Baek, and W. Lee (2004) Chiral discrimination studies of (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid by high-performance liquid chromatography and NMR spectroscopy. Magn. Reson. Chem. 42: 389-395.
DOI
|
17 |
Lee, T., W. Lee, M. H. Hyun, and J. H. Park (2010) Enantioseparation of native -amino acids on an 18-crown-6-tetracarboxylic acidbonded silica by capillary electrochromatography. J. Chromatogr. A. 1217: 1425-1428.
DOI
|
18 |
Jeon, S. H., M. H. Kim, H.-K. Han, and W. Lee (2010) Direct enantiomer separation of thyroxine in pharmaceuticals using crown ether type chiral stationary phase. Arch. Pharm. Res. 33: 1419-1423.
과학기술학회마을
DOI
|
19 |
Jeon, S. H. and W. Lee (2010) Monitoring of the optical purity for levothyroxine sodium in pharmaceuticals using crown ether derived chiral columns. KSBB J. 25: 449-452.
과학기술학회마을
|
20 |
Jin, J. Y., C.-S. Baek, and W. Lee (2007) Development of a validated HPLC method for the simultaneous determination of D- and L-thyroxine in human plasma. Bull. Kor. Chem. Soc. 28: 1070-1072.
과학기술학회마을
DOI
|
21 |
Lee, W. (2009) The application of chiral HPLC columns for enantiomer separation of chiral drugs. Yakhak Hoeji. 53: 60-68.
과학기술학회마을
|
22 |
Kim, K. J., I. Choi, K. Seo, H.-K. Han, and W. Lee (2011) Regulatory requirements on the safety and efficacy evaluation for the development of stereoisomeric drugs. Yakhak Hoeji. 55: 426-431.
과학기술학회마을
|
23 |
Vogtle, F. and E. Weber (1985) Host Guest Complex Chemistry-Macrocycles, pp. 1-41. Springer-Verlag, Berlin.
|
24 |
Pedersen, C. J. (1967) Cyclic polyethers and their complexes with metal salts. J. Am. Chem. Soc. 89: 2495-2496.
DOI
|
25 |
Cram, D. J. (1988) The design of molecular hosts, guests, and their complexes. Angew. Chem. Int. Engl. 27: 1009-1020.
DOI
|
26 |
Zhang, X.-X., J. S. Bradshaw, and R. M. Izatt (1997) Enantiomeric recognition of amine compounds by chiral macrocyclic receptors. Chem. Rev. 97: 3313-3362.
DOI
|
27 |
Shinbo, T., T. Yamaguchi, K. Nishimura, and M. Sugiura (1987) Chromatographic separation of racemic amino acids by use of chiral crown ether-coated reversed-phase packings. J. Chromatogr. A. 405: 145-153.
DOI
|
28 |
Application guide for chiral HPLC selection, 3rd Ed., (2002) Daicel Chemical Industries, Ltd.
|
29 |
Lee, W. and C. Y. Hong (2000) Direct liquid chromatographic enantiomer separation of new fluoroquinolones including gemifloxacin. J. Chromatogr. A. 879: 113-120.
DOI
|
30 |
Shinbo, T., T. Yamaguchi, H. Yanagishita, D. Kitamoto, K. Sakaki, and M. Sugiura (1992) Improved crown ether-based chiral stationary phase. J. Chromatogr. A. 625: 101-108.
DOI
|
31 |
Hyun, M. H., S. C. Han, B. H. Lipshutz, Y.-J. Shin, and C. J. Welch (2001) New chiral crown ether stationary phase for the liquid chromatographic resolution of -amino acid enantiomers. J. Chromatogr. A. 910: 359-365.
DOI
|
32 |
Kuhn, R., J. Wagner, Y. Walbroehl, and T. Bereuter (1994) Potential and limitations of an optically active crown ether for chiral separation in capillary zone electrophoresis. Electrophoresis. 15: 828-834.
DOI
|
33 |
Hyun, M. H. (2006) Preparation and application of HPLC chiral stationary phases based on (+)-(18-crown-6)-2,3,11,12- tetracarboxylic acid. J. Sep. Sci. 29: 750-761.
DOI
|
34 |
Hyun, M. H. (2005) Development and application of crown ether-based HPLC chiral stationary phases. Bull. Kor. Chem. Soc. 26: 1153-1631.
과학기술학회마을
DOI
|
35 |
Kuhn, R., F. Erni, T. Bereuter, and J. Hausler (1992) Chiral recognition and enantiomeric resolution based on host-guest complexation with crown ethers in capillary zone electrophoresis. Anal. Chem. 64: 2815-2820.
DOI
|
36 |
Behr, J.-M., J.-M. Girodeau, R. C. Heyward, J.-M. Lehn, and J.-P. Sauvage (1980) Molecular receptors. functionalized and chiral macrocyclic polyethers derived from tartaric acid. Helv. Chim. Acta. 63: 2096-2111.
DOI
|
37 |
Lee W., S. La, Y. Choi, and K.-R. Kim (2003) Chiral discrimination of aromatic amino acids by capillary electrophoresis in (+)- and (-)-(18-crown-6)-2,3,11,12-tetracarboxylic acid selector modes. Bull. Kor. Chem. Soc. 24: 1232-1234.
과학기술학회마을
DOI
|
38 |
Park H.-J., Y. Choi, W. Lee, and K.-R. Kim (2004) Enantioseparation of aromatic amino acids and amino acid esters by capillary electrophoresis with crown ether and prediction of enantiomer migration orders by a three-dimensional quantitative structureproperty relationship/comparative field analysis model. Electrophoresis 25: 2755-2760.
DOI
|
39 |
Paik, M.-J. and W. Lee, Unpublished results.
|