References
-
Bai, D., Xu, R., Chu, G., and Zhu, X. Synthesis of (
$\pm$ )-epibatidine and its analogues. J. Org. Chem., 61, 4600-4606 (1996) https://doi.org/10.1021/jo9600666 - Barros, M. T., Maycock, C. D., and Ventura, M. R. The effect of DMSO on the borohydride reduction of a cyclohexanone: A formal enantioselective synthesis of (+)-epibatidine. Tetrahedron Lett., 40, 557-560 (1999) https://doi.org/10.1016/S0040-4039(98)02354-5
-
Che, D., Wegge, T., Stubbs, M. T, Seitz, G., Meier, H., and Methfessel, C. exo-2-(Pyridazin4-y1)-7-azabicyclo[2.2.1]heptanes: Syntheses and nicotinic acetylation receptor agonist activity of potent pyridazine analogues of (
$\pm$ )-epibatidine. J. Med. Chem. 44, 47-57 (2001) https://doi.org/10.1021/jm000949w - Evans, D. A., Scheidt, K. A., and Downey, C. W. Synthesis of (-) -epibatidine. Organic Lett., 3, 3009-3012 (2001) https://doi.org/10.1021/ol016420q
- Fisher, M., Huang, D. F., Shen, T. Y., and Guyenet, P. G. J. Pharmcol. Exp. Ther., 270, 702-707 (1994)
-
Ham, W. H., Kim, Y. H., Won, D. Y., Oh, C. Y, Lee, K. Y., Jeong, J. H., and Jung, Y. H. Total synthesis of (
$\pm$ )-homoepibatidine. Arch. Pharm. Res., 22, 435-436 (1999) https://doi.org/10.1007/BF02979073 -
Helquist, P., Palmgren, A., Larsson, A. L. E., and Backvall, J-E. Paliadium(II)-Catalyzed 1,4-Oxidatior of 2-Aryl-1,3-cyclohexadienes. Application to the Synthesis of (
$\pm$ )-Epibatidine and Analogues. J. Org. Chem., 64, 836-842 (1999) https://doi.org/10.1021/jo981668n - Ivy Carroll, F., Liang, F., Navaro, H. A., Brieaddy, L. E., Abraham, P., Damaj, M. I., and Martin, B. R. Synthesis, nicotinic acetylcholine receptor binding, and anti nociceptive properties of 2-exo- 2-(2'-substituted 5'-pyridinyl)-7-azabicyclo[2.2.1]heptanes. epibatidine analogues. J. Med. Chem. 44, 2229-2237 (2001) https://doi.org/10.1021/jm0100178
- Koren, A. O., Horti, A. G., Mukhin, A. G., Gundisch, D., Kimes, A. S., Dannals, R. F., London, E. D. 2-, 5-, and 6-halo-3-(2(S)-azetidinylmethoxy)pyridines: Synthesis, affinity for nicotinic acetylcholine receptors, and molecular modeling. J. Med. Chem., 41, 3690-3698 (1999)
- Malpass, J. R., Hemmings, D. A., and Wallis, A. L. Synthesis of epibatidine homoloues. Tetrahedron Lett., 37, 3911-3914 (1996) https://doi.org/10.1016/0040-4039(96)00687-9
- Malpass, J. R. and Cox, C. D. Synt'iesis of 5- and 6-chloropyridyl- substituted 2-azabicyclo[2.2.1]heptanes; novel epibatidine isomers. Tetrahedron Lett., 40, 1419-1422 (1999). https://doi.org/10.1016/S0040-4039(98)02624-0
- Mann, J., Barbosa, L-C de A. An efficient route to the tropane alkaloids. J. Chem. Soc. Perkin Trans. 1., 787-789 (1992)
-
Methfessel, C., Che, D., Wegge, T., Stubbs, M. T, Seitz, G., and Meier, H. exo-2-(Pyridazin-4-yl)-7-azabicyclo[2.2.1]heptanes: syntheses and nicotinic acetylcholine receptor agonist activity of potent pyridazine analogues of (
$\pm$ )-Epibatidine. J. Med. Chem., 44, 47-57 (2001) https://doi.org/10.1021/jm000949w - Pandey, G., Bagul, T. D., and Sahoo, A. K. [3+2] Cycloaddition of nonstabilized azomethine ylides. Stereoselective synthesis of epibatidine and analogues. J. Org. Chem.,63, 760-768 (1998) https://doi.org/10.1021/jo971728+
- Qian, C., Li, T, Shen, T. Y., Libertine-Garaham, L., Eckman, J., and Biftu, T., Ip, S. Eur. J. Pharmacol., 250, R13-R14 (1993) https://doi.org/10.1016/0014-2999(93)90043-H
- Olivo, H. F., Colby, D. A., and Hemenway, M. S. Syntheses of new open-ring and homo-epibatidine analogues from tropinone J. Org. Chem., 64, 4966-4968 (1999) https://doi.org/10.1021/jo990097b
- Rasmussen, J. R., Slinger, C. J., Kordish, R. J., and NewmanEvans, D. D. Synthesis of deoxy sugars. J. Org. Chem., 46, 4843-4846 (1981) https://doi.org/10.1021/jo00337a004
- Spande, T. F., Garraffo, H. M., Edwards, M. W., Ych, H. J. C., Pannel, L., Daly, and J. W. Epibatidine: A novel (chloropyridyl) azabicycloheptane with potent analgesic activity from an ecuandoran poison fog. J. Am. Chem. Soc. 114, 3475-3478 (1992) https://doi.org/10.1021/ja00035a048
- Zhang C., Gyermek, L., and Trudell, M. L. Synthesis of optically pure epibatidine analogs. Tetrahedron Lett., 38, 5619-5622 (1997) https://doi.org/10.1016/S0040-4039(97)01276-8