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32
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0010617047
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note
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12. The depicted structures (specified by bold arabic numbers) represent also the absolute configuration of the corresponding molecules. An enantiomeric structure is specified by adding the prefix ent-to the bold arabic number.
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0002050576
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35
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0010614581
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note
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9a,18.
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36
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0003942864
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Wiley, New York
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15. For the dependency of the enantiomeric excess on the conversion in kinetic resolutions, see, for example: Eliel, E.L.; Wilen, S.H. Stereochemistry of Organic Compounds, Wiley, New York 1994, pp. 395.
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Eliel, E.L.1
Wilen, S.H.2
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37
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0010548107
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note
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3 in the presence of 0.3 eq 3a (73% conversion). In this case, the re-isolated ketone complex (4a) had an enantiomeric purity of 98% e.e..
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38
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0346267223
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17. Mathre, D.J.; Jones, T.K.; Xavier, L.C.; Blacklock, T.J.; Reamer, R.A.; Mohan, J.J.; Jones, E.T.T.; Hoogsteen, K.; Baum, M.W.; Grabowski, E.J.J. J. Org. Chem., 1991, 56, 751.
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Mohan, J.J.6
Jones, E.T.T.7
Hoogsteen, K.8
Baum, M.W.9
Grabowski, E.J.J.10
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