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1. Synthetic Studies Towards the Indole Alkaloid Tacamine, Part 4. For Part 3, see ref. 11.
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(b) Delaude, C.; Thépenier, P.; Jacquier, M.-J.; Massiot, G.; Le Men-Olivier, L. Bull. Soc. R. Sci. Liège 1992, 61, 429-440;
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0001084272
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See also ref. 15b
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(c) Bruix, M.; Rumbero, A.; Vázquez, P. Phytochem. 1993, 33, 1257-1261. See also ref. 15b.
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28
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85030268494
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Protection of the hydroxyl group (e.g. as an acetate) leads to the loss of this moiety in the catalytic hydrogenation, possibly via the following mechanism: (formula presented)
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22. Protection of the hydroxyl group (e.g. as an acetate) leads to the loss of this moiety in the catalytic hydrogenation, possibly via the following mechanism: (formula presented)
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85030280179
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The complete NMR characterization of these diastereomeric alcohols, including determination of configuration at the hydroxyethyl side chain, will be reported elsewhere
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23. The complete NMR characterization of these diastereomeric alcohols, including determination of configuration at the hydroxyethyl side chain, will be reported elsewhere.
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0000295212
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24. Frigerio, M.; Santagostino, M.; Sputore, S.; Palmisano, G. J. Org. Chem. 1995, 60, 7272-7276.
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0011810157
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Atta-ur-Rahman, Ed. Elsevier, Amsterdam
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25. See e.g.: Lounasmaa, M. in Studies in Natural Products Chemistry (Atta-ur-Rahman, Ed.), Vol. 14, Elsevier, Amsterdam, 1994, p. 712.
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Studies in Natural Products Chemistry
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Lounasmaa, M.1
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