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33845555986
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For recent reports concerning the biological utility of the 1- and 2-azabicyco[2.2.2]octane ring systems, see
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(e): 3-Azabicyclo[3.3.1]nonanes: Jeyaraman, R.; Avila, S. Chem. Rev. 1981, 81, 149. For recent reports concerning the biological utility of the 1- and 2-azabicyco[2.2.2]octane ring systems, see:
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(3) For recent syntheses of 6-azabicyclo[3.2.2]nonanes: (a) Lowe III, J. A.; Drozda, S. E.; McLean, S.; Bryce, D. K.; Crawford, R. T; Snider, R. M.; Longo, K. P.; Nagahisa, A.; Tsuchiya, M. J. Med. Chem. 1994, 37, 2831.
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14
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0010632331
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note
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2O) to give 5a (2.69 g, 8.98 mmol, 30%) and 6a (2.59 g, 8.64 mmol, 29%).
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15
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0026590813
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(6) Hashimoto, S.; Watanabe, N.; Ikegami, S. Tetrahedron Lett. 1992, 33, 2709.
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Hashimoto, S.1
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(7) (a) Davies, H. M. L.; Ahmed, G.; Churchill, M. R. J. Am. Chem. Soc. 1996, 118, 10774.
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Davies, H.M.L.1
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(c) Davies, H. M. L.; Peng, Z.; Houser, J. H. Tetrahedron Lett. 1994, 35, 8939.
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Davies, H.M.L.1
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20
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0029945485
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and references therein
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(8) Davies, H. M. L.; Bruzinski, P. R.; Lake, D. H.; Kong, N.; Fall, M. J. J. Am. Chem. Soc. 1996, 118, 6897, and references therein.
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Davies, H.M.L.1
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Fall, M.J.5
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0029084414
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(b) Williams, J. M.; Jobson, R. B.; Yasuda, N.; Marchesini, G.; Dolling, U.-H.; Grabowski, E. J. J. Tetrahedron Lett. 1995, 31, 5461.
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Williams, J.M.1
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Grabowski, E.J.J.6
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