none 10.3987/COM-01-9194 CLOCKSS Archive CLOCKSS Archive 5187 36504852 73640 20090309141854 10.13030 2024-06-24T20:32:42Z 2009-03-09T05:19:43Z 2 HETEROCYCLES HETEROCYCLES 0385-5414 HTCYAM 2001 55 6 Andrew Coop Dean Y. Maeda 2001 1147 COM-01-9194 10.3987/COM-01-9194 20090309141854 https://triggered.stanford.clockss.org/ServeContent?doi=10.3987%2Fcom-01-9194 https://triggered.edinburgh.clockss.org/ServeContent?doi=10.3987%2Fcom-01-9194 10.1007/978-1-4899-0585-7 1. A. F. Casy and R. T. Parfitt, Opioid Analgesics, Plenum Press, New York and London, 1986. 2. J. W. Lewis, Buprenorphine - Medicinal Chemistry, in Buprenorphine: Combating Drug Abuse with a Unique Opioid, ed. by A. Cowan and J. W. Lewis, 1995, pp. 3-6, Wiley-Liss, New York. 10.1016/S0014-2999(99)00758-X 3. M. D. Aceto, S. M. Scates, L. S. Harris, and Z. Li, Eur. J. Pharmacol., 2000, 387, 31. 10.1016/S0960-894X(99)00085-2 4. S. M. Husbands, S. W. Breedon, K. Grivas, and J. W. Lewis, Bioorg. Med. Chem. Lett., 1999, 9, 831. 5. J. R. Traynor, L. Guo, A. Coop, J. W. Lewis, and J. H. Woods, J. Pharmacol. Exp. Ther., 1999, 291, 1093. 10.1021/jm991165p 6. S. M. Husbands and J. W. Lewis, J. Med. Chem., 2000, 43, 139. 7. J. W. Lewis, M. J. Readhead, and A. C. B. Smith, J. Med. Chem., 1973, 16, 9. 10.1039/J39690002229 8. K. W. Bentley, D. G. Hardy, B. Meek, and J. B. Traynor, J. Chem. Soc. C, 1969, 2229. 9. A. Coop, K. Grivas, S. Husbands, and J. W. Lewis, Tetrahedron, 1995, 51, 9681. 10.1016/S0040-4039(01)84256-8 10. D. A. Evans, W. L. Scott, and L. K. Truesdale, Tetrahedron Lett., 1972, 121. 11. N. C. Madge and A. B. Holmes, J. Chem. Soc., Chem. Commun., 1980, 956. 10.1039/J39710001158 J. W. Lewis, M. J. Readhead, I. A. Selby, A. C. B. Smith, and C. A. Young, J. Chem. Soc., 1971, 1158. 12. The yield of this reaction was 67%. The melting point, NMR and MS data were consistent with literature values for cyanochloro adduct (4). 13. The yield of this reaction was 67%. The melting point, NMR and MS data were consistent with literature values for cyanochloro adduct (4).