References
- Crossley, R. Chirality and the Biological Activity of Drugs; CRC Press: Boca Raton, 1995
- Announcement. Chirality 1992, 4, 338 https://doi.org/10.1002/chir.530040513
- DeCamp, W. H. J. Pharm. Biomed. Anal. 1993, 11, 1167 https://doi.org/10.1016/0731-7085(93)80100-F
- Tomaszewski, J.; Rumore, M. M. Drug Dev. Ind. Pharm. 1994, 20, 119 https://doi.org/10.3109/03639049409039080
- Chiral Separations: Applications and Technology; Ahuja, S., Ed.; American Chemical Society: Washington, DC, 1997
- Chiral Separation Techniques: A Practical Approach; Subramanian, G., Ed.; Wiely-VCH: Weinheim, 2001
- Chiral Separations: Methods and Protocols; Gubitz, G.; Schmid, M. G., Eds.; Humana Press: Totowa, New Jersey, 2004
- Beesley, T. E.; Scott, R. P. W. Chiral Chromatography; John Wiely & Sons: New York, 1998
- Ahuja, S. Chiral Separations by Chromatography; American Chemical Society, Oxford University Press: Oxford, 2000
- Aboul-Enein, H. Y.; Ali, I. Chiral Separations by Liquid Chromatography and Related Technologies; Marcel Dekker: New York, 2003
- Miwa, T.; Ichikawa, M.; Tsuno, M.; Hattori, T.; Miyakawa, T.; Kayano, M.; Miyake, Y. Chem. Pharm. Bull. 1987, 35, 682 https://doi.org/10.1248/cpb.35.682
- Allenmark, S. J. Liq. Chromatogr. 1986, 9, 425
- Okamoto, Y.; Kawashima, M.; Hatada, K. J. Am. Chem. Soc. 1984, 106, 5357 https://doi.org/10.1021/ja00330a057
- Ward, T. J.; Armstrong, D. W. J. Liq. Chromatogr. 1986, 9, 407 https://doi.org/10.1080/01483918608076644
- Armstrong, D. W.; Tang, Y.; Chen, S.; Zhou, Y.; Bagwill, C.; Chen, J. R. Anal. Chem. 1994, 66, 1473 https://doi.org/10.1021/ac00081a019
- Ward, T. J.; Farris, A. B. J. Chromatogr. A 2001, 906, 73 https://doi.org/10.1016/S0021-9673(00)00941-9
- Pirkle, W. H.; Finn, J. M.; Schreiner, J. L.; Hamper, B. C. J. Am. Chem. Soc. 1981, 103, 3964 https://doi.org/10.1021/ja00403a076
- Pirkle, W. H.; Pochapsky, T. C. J. Am. Chem. Soc. 1986, 108, 352 https://doi.org/10.1021/ja00262a059
- Hyun, M. H.; Kang, M. H.; Han, S. C. J. Chromatogr. A 2000, 868, 31 https://doi.org/10.1016/S0021-9673(99)01140-1
- Hyun, M. H.; Cho, Y. J.; Choi, H. J.; Lee, K. W. Bull. Korean Chem. Soc. 2004, 25, 1977 https://doi.org/10.5012/bkcs.2004.25.12.1977
- Pirkle, W. H.; Welch, C. J.; Lamm, B. J. Org. Chem. 1992, 57, 3854 https://doi.org/10.1021/jo00040a026
- Gasparrini, F.; Misiti, D.; Villani, C. J. Chromatogr. A 2001, 906, 35 https://doi.org/10.1016/S0021-9673(00)00953-5
- Hyun, M. H.; Kim, J. I.; Cho, Y. J.; Ryoo, J.-J. Bull. Korean Chem. Soc. 2004, 25, 1707 https://doi.org/10.5012/bkcs.2004.25.11.1707
- Hyun, M. H. J. Sep. Sci. 2003, 26, 242 https://doi.org/10.1002/jssc.200390030
- Pederson, C. J. J. Am. Chem. Soc. 1967, 89, 2495 https://doi.org/10.1021/ja00986a052
- Pederson, C. J. J. Am. Chem. Soc. 1967, 89, 7017 https://doi.org/10.1021/ja01002a035
- Izatt, R. M.; Terry, R. E.; Haymore, B. L.; Hansen, L. D.; Dalley, N. K.; Avondet, A. G.; Christensen, J. J. J. Am. Chem. Soc. 1976, 98, 7620 https://doi.org/10.1021/ja00440a028
- Gokel, G. W.; Leevy, W. M.; Weber, M. E. Chem. Rev. 2004, 104, 2723 https://doi.org/10.1021/cr020080k
- Kyba, E. P.; Siegel, M. G.; Sousa, L. R.; Sogah, G. D. Y.; Cram, D. J. J. Am. Chem. Soc. 1973, 95, 2691 https://doi.org/10.1021/ja00789a050
- Kyba, E. P.; Koga, K.; Sousa, L. R.; Siegel, M. G.; Cram, D. J. J. Am. Chem. Soc. 1973, 95, 2692 https://doi.org/10.1021/ja00789a051
- Kyba, E. P.; Timko, J. M.; Kaplan, L. J.; de Jong, F.; Gokel, G. W.; Cram, D. J. J. Am. Chem. Soc. 1978, 100, 4555 https://doi.org/10.1021/ja00482a040
- Lingenfelter, D. S.; Helgeson, R. C.; Cram, D. J. J. Org. Chem. 1981, 46, 393 https://doi.org/10.1021/jo00315a033
- Yamamoto, K.; Noda, K.; Okamoto, Y. J. Chem. Soc., Chem. Commun. 1985, 1065
- Yamamoto, K.; Kitsuki, T.; Okamoto. Y. Bull. Chem. Soc. Jpn. 1986, 59, 1269 https://doi.org/10.1246/bcsj.59.1269
- Yamamoto, K.; Yumioka, H.; Okamoto, Y.; Chikamatsu, H. J. Chem. Soc., Chem. Commun. 1987, 168
- Nakazaki, M.; Yamamoto, K.; Ikeda, T.; Kitsuki, T.; Okamoto, Y. J. Chem. Soc., Chem. Commun. 1983, 787
- Behr, J.-M.; Girodeau, J.-M.; Heyward, R. C.; Lehn, J.-M.; Sauvage, J.-P. Hel. Chim. Acta 1980, 63, 2096 https://doi.org/10.1002/hlca.19800630736
- Gehin, D.; Cesare, P. D.; Gross, B. J. Org. Chem. 1986, 51, 1906 https://doi.org/10.1021/jo00360a050
- Demirel, N.; Bulut, Y. Tetrahedron Asymmetry 2003, 14, 2633 https://doi.org/10.1016/S0957-4166(03)00594-9
- Turgut, Y.; Hosgoren, H. Asymmetry 2003, 14, 3815 https://doi.org/10.1016/j.tetasy.2003.09.037
- Davidson, R. B.; Bradshaw, J. S.; Jones, B. A.; Dalley, K. N.; Christensen, J. J.; Izatt, R. M.; Morin, F. G.; Grant, D. M. J. Org. Chem. 1984, 49, 353 https://doi.org/10.1021/jo00176a026
- Hirose, K.; Fujiwara, A.; Matsunaga, K.; Aoki, N.; Tobe, Y. Tetrahedron Asymmetry 2003, 14, 555 https://doi.org/10.1016/S0957-4166(03)00031-4
- Sogah, G. D. Y.; Cram, D. J. J. Am. Chem. Soc. 1975, 97, 1259 https://doi.org/10.1021/ja00838a059
- Sousa, L. R.; Sogah, G. D. Y.; Hoffman, D. H.; Cram, D. J. J. Am. Chem. Soc. 1978, 100, 4569 https://doi.org/10.1021/ja00482a041
- Sogah, G. D. Y.; Cram, D. J. J. Am. Chem. Soc. 1976, 98, 1976
- Sogah, G. D. Y.; Cram, D. J. J. Am. Chem. Soc. 1979, 101, 3035 https://doi.org/10.1021/ja00505a034
- Shinbo, T.; Yamaguchi, T.; Nishimura, K.; Sugiura, M. J. Chromatogr. 1987, 405, 145 https://doi.org/10.1016/S0021-9673(01)81756-8
- Aboul-Enein, H. Y.; Seringnese, V. Biomed. Chromatogr. 1995, 9, 98 https://doi.org/10.1002/bmc.1130090209
- Aboul-Enein, H. Y.; Seringnese, V. Biomed. Chromatogr. 1997, 11, 7 https://doi.org/10.1002/(SICI)1099-0801(199701)11:1<7::AID-BMC607>3.0.CO;2-F
- Walbroehl, Y.; Wagner, J. J. Chromatogr. A 1994, 680, 253 https://doi.org/10.1016/0021-9673(94)80075-8
- Nishi, H.; Nakamura, K.; Nakai, H.; Sato, T. J. Chromatogr. A 1997, 757, 225 https://doi.org/10.1016/S0021-9673(96)00667-X
- Kersten, B. S. J. Liq. Chromatogr. 1994, 17, 33 https://doi.org/10.1080/10826079408013434
- Peter, A.; Lazar, L.; Fulop, F.; Armstrong, D. W. J. Chromatogr. A 2001, 926, 229 https://doi.org/10.1016/S0021-9673(01)01078-0
- Lee, W.; Hong, C. Y. J. Chromatogr. A 2000, 879, 113 https://doi.org/10.1016/S0021-9673(00)00322-8
- 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
- Lipshutz, B. H.; Shin, Y.-J. Tetrahedron Lett. 1998, 39, 7017 https://doi.org/10.1016/S0040-4039(98)01468-3
- 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
- Lehn, J.-M. J. Incl. Phenom. 1988, 6, 351 https://doi.org/10.1007/BF00658981
- Cram, D. J. J. Incl. Phenom. 1988, 6, 397 https://doi.org/10.1007/BF00658982
- Udvarhelyi, P. M.; Watkins, J. C. Chirality 1990, 2, 200 https://doi.org/10.1002/chir.530020313
- Okamoto, M.; Takahashi, K.-I.; Doi, T. J. Chromatogr. A 1994, 675, 244 https://doi.org/10.1016/0021-9673(94)85279-0
- Remelli, M.; Bovi, C.; Pulidori, F. Annali di Chimica 1999, 89, 107
- Thompson, R. A.; Ge, Z.; Grinberg, N.; Ellison, D.; Tway, P. Anal. Chem. 1995, 67, 1580 https://doi.org/10.1021/ac00105a017
- Machida, Y.; Nishi, H.; Kakamura, K. J. Chromatogr. A 1999, 830, 311 https://doi.org/10.1016/S0021-9673(98)00896-6
- Kuhn, R.; Erni, F.; Bereuter, T.; Hausler, J. Anal. Chem. 1992, 64, 2815 https://doi.org/10.1021/ac00046a026
- Kuhn, R.; Stoecklin, F.; Erni, F. Chromatographia 1992, 33, 32 https://doi.org/10.1007/BF02276847
- Kuhn, R.; Hoffstetter-Kuhn, S. Chromatographia 1992, 34, 505 https://doi.org/10.1007/BF02290245
- Kuhn, R.; Steinmetz, C.; Bereuter, T.; Haas, P.; Erni, F. J. Chromatogr. A 1994, 666, 367 https://doi.org/10.1016/0021-9673(94)80396-X
- Kuhn, R. Electrophoresis 1999, 20, 2065 https://doi.org/10.1002/(SICI)1522-2683(19990701)20:10<2065::AID-ELPS2065>3.0.CO;2-E
- Walbroehl, Y.; Wagner, J. J. Chromatogr. A 1994, 685, 321 https://doi.org/10.1016/0021-9673(94)00722-5
- Schmid, M. G.; Gubitz, G. J. Chromatogr. A 1995, 709, 81 https://doi.org/10.1016/0021-9673(95)00106-W
- Lin, J.-M.; Nakamura, T.; Hobo, T. Chromatographia 1996, 42, 559 https://doi.org/10.1007/BF02290292
- Mori, Y.; Ueno, K.; Umeda, T. J. Chromatogr. A 1997, 757, 328 https://doi.org/10.1016/S0021-9673(96)00674-7
- Verleysen, K.; Vandijck, J.; Schelfaut, M.; Sandra, P. J. High Resol. Chromatogr. 1998, 21, 323 https://doi.org/10.1002/(SICI)1521-4168(19980601)21:6<323::AID-JHRC323>3.0.CO;2-V
- Cho. S. I.; Lee, K.-N.; Kim, Y.-K.; Jang, J.; Chung, D. S. Electrophoresis 2002, 23, 972 https://doi.org/10.1002/1522-2683(200203)23:6<972::AID-ELPS972>3.0.CO;2-F
- Cho, S. I.; Shim, J.; Kim, M.- S.; Kim, Y.-K.; Chung, D. S. J. Chromatogr. A 2004, 1055, 241
- Machida, Y.; Nishi, H.; Nakamura, K.; Nakai, H.; Sato, T. J. Chromatogr. A 1998, 805, 82
- Hyun, M. H.; Jin, J. S.; Lee, W. Bull. Korean Chem. Soc. 1998, 19, 819
- Hyun, M. H.; Jin, J. S.; Lee, W. J. Chromatogr. A 1998, 822, 155 https://doi.org/10.1016/S0021-9673(98)00606-2
- Cross, G. G.; Fyles, T. M. J. Org. Chem. 1997, 62, 6226 https://doi.org/10.1021/jo970707c
- Aboul-Enein, H. Y.; Ali, I.; Hyun, M. H.; Cho, Y. J.; Jin, J. S. J. Biochem. Biophys. Methods 2002, 54, 407 https://doi.org/10.1016/S0165-022X(02)00142-2
- 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
- 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.; Min, H. J.; Cho, Y. J. Bull. Korean Chem. Soc. 2003, 24, 911 https://doi.org/10.5012/bkcs.2003.24.7.911
- 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
- Hyun, M. H.; Tan, G.; Cho, Y. J. J. Liq. Chromatogr. Rel. Technol. 2004, 27, 1671 https://doi.org/10.1081/JLC-120037363
- Steffeck, R. J.; Zelechonok, Y.; Gahm, K. H. J. Chromatogr. A 2002, 947, 301 https://doi.org/10.1016/S0021-9673(01)01604-1
- Machida, Y.; Nishi, H.; Nakamura, K. J. Chromatogr. A 1998, 810, 33 https://doi.org/10.1016/S0021-9673(98)00207-6
- Bang, E.; Jung, J.-W.; Lee, W.; Lee, D. W.; Lee, W. J. Chem. Soc. Perkin Trans. 2 2001, 1685
- Machida, Y.; Nishi, H.; Nakamura, K. Chirality 1999, 11, 173 https://doi.org/10.1002/(SICI)1520-636X(1999)11:3<173::AID-CHIR1>3.0.CO;2-P
- Hyun, M. H.; Jin, J. S.; Han, S. C.; Cho, Y. J. Microchem. J. 2001, 70, 205 https://doi.org/10.1016/S0026-265X(01)00134-5
- Hyun, M. H.; Koo, H. J.; Jin, J. S.; Lee, W. J. Liq. Chromatogr. & Rel. Technol. 2000, 23, 2669 https://doi.org/10.1081/JLC-100101825
- Zhang, D.; Li, F.; Kim, D. H.; Choi, H. J.; Hyun, M. H. J. Chromatogr. A 2005, 1083, 89 https://doi.org/10.1016/j.chroma.2005.06.038
- Hyun, M. H.; Cho, Y. J.; Kim, J. A.; Jin, J. S. J. Chromatogr. A 2003, 984, 163 https://doi.org/10.1016/S0021-9673(02)01833-2
- Gehin, D.; Kollman, P. A.; Wipff, G. J. Am. Chem. Soc. 1989, 111, 3011 https://doi.org/10.1021/ja00190a040
- Hyun, M. H.; Kim, D. H. Chirality 2004, 16, 294 https://doi.org/10.1002/chir.20038
- Hyun, M. H.; Kim, Y. H.; Cho, Y. J. Bull. Korean 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
- Hyun, M. H.; Kim, D. H.; Cho, Y. J.; Jin, J. S. J. Sep. Sci. 2005, 28, 421 https://doi.org/10.1002/jssc.200401951
- Naemura, K.; Fuji, J.; Ogasahara, K.; Hirose, K.; Tobe, Y. Chem. Commun. 1996, 2749
- Naemura, K.; Nishioka, K.; Ogasahara, K.; Nishikawa, Y.; Hirose, K.; Tobe, Y. Tetrahedron Asymmetry 1998, 9, 563 https://doi.org/10.1016/S0957-4166(97)00638-1
- Hirose, K.; Ogasahara, K.; Nishioka, K.; Tobe, Y.; Naemura, K. J. Chem. Soc., Perkin Trans. 2 2000, 1984
- Hirose, K.; Nakamura, T.; Nishioka, R.; Ueshige, T.; Tobe, Y. Tetrahedron Lett. 2003, 44, 1549 https://doi.org/10.1016/S0040-4039(03)00020-0
- Hirose, K.; Yongzhu, J.; Nakamura, T.; Nishioka, R.; Ueshige, T.; Tobe, Y. Chirality 2005, 17, 142 https://doi.org/10.1002/chir.20138
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