참고문헌
- Marrs, T. C. Pharmacol. Ther. 1993, 58, 51-66. https://doi.org/10.1016/0163-7258(93)90066-M
- Dawson, R.M. J. Appl. Toxicol. 1994, 14, 317-331. https://doi.org/10.1002/jat.2550140502
- Bajgar, J. Acta Med. 1996, 39, 101-105.
- Leadbeater, L.; Inns, R. H.; Rylands, J. M. Fundam. Appl.Toxicol. 1985, 5, S225-231. https://doi.org/10.1016/0272-0590(85)90132-0
- Thiermann, H.; Seidl, S.; Eyer, P. Int. J. Pharm. 1996, 137,167-176. https://doi.org/10.1016/0378-5173(96)04511-5
- Aas, P. Eur. J. Pharmcol. 1996, 301, 59-66. https://doi.org/10.1016/0014-2999(96)00027-1
- Lallement, G.; Clarencon, D.; Brochier, G.; Baubichon, D.;Galonnier, M.; Blanchet, G.; Mestries, J. Pharmacol. Biochem.Behav. 1997, 56, 325-332. https://doi.org/10.1016/S0091-3057(96)00292-4
- Hagedorn, I. USP 3,852,294, 1974.
- Burness, D. M.; Wright, C. J.; Perkins, W. C. J. Org. Chem.1977, 42, 2910-2913. https://doi.org/10.1021/jo00437a028
- Wadsworth, D. H.; Vinal, R. S. J. Org. Chem. 1982, 47, 1623-1626. https://doi.org/10.1021/jo00348a003
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