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5. von Riesen, C.; Jones, P. G.; Hoffmann, H. M. R. Chem. Eur. J. 1995, 2, 673. For the synthesis of further tricyclic Cinchona alkaloids containing a 1,3-diketo-2-N,O-acetal functionality see Langer, P.; Frackenpohl, J.; Hoffmann, H. M. R. J. Chem. Soc., Perkin Trans. 1 1998, in press.
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5. von Riesen, C.; Jones, P. G.; Hoffmann, H. M. R. Chem. Eur. J. 1995, 2, 673. For the synthesis of further tricyclic Cinchona alkaloids containing a 1,3-diketo-2-N,O-acetal functionality see Langer, P.; Frackenpohl, J.; Hoffmann, H. M. R. J. Chem. Soc., Perkin Trans. 1 1998, in press.
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7 Langer, P.; Hoffmann, H. M. R. Tetrahedron 1997, 53, 9145-9158; see also Rowan, S. J.; Brady, P. A.; Sanders, J. K. M. Angew. Chem. 1996, 108, 2283; Angew. Chem. Int. Ed. Engl. 1996, 35, 2143.
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15. Carroll, F. I.; Abraham, P.; Gaetano, K.; Mascarella, S. W.; Wohl, R. A.; Lind, J.; Petzoldt, K. J. Chem. Soc., Perkin Trans. 1 1991, 3017; von Riesen, C.; Hoffmann, H. M. R. Chem. Eur. J. 1996, 2, 680.
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0010611574
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note
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16. Chemical Abstracts name of rubanone 7: {1R-[-(1α,4α,6β(S*)]}-6-[Hydroxy-(6-methoxy-4-quinolinyl)methyl]-1-azabicyclo[2.2.2]octan-3-one. Our numbering of Cinchona alkaloids follows the Cinchona convention as indicated in Scheme 2.
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