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33646956349
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note
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13a the configuration at C2 was established to be R. Details are provided in the Supporting Information.
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28
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37049110949
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For 28, see the following: Boehlein, S. K.; Rosa-Rodriguez, J. G.; Schuster, S. M.; Richards, N. G. J. J. Am. Chem. Soc. 1997, 119, 5785.
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44
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33646959313
-
-
The corresponding (R)-29 was prepared from D-24 in an analogous fashion and utilized for the preparation of 55 as detailed in Scheme 9
-
The corresponding (R)-29 was prepared from D-24 in an analogous fashion and utilized for the preparation of 55 as detailed in Scheme 9.
-
-
-
-
47
-
-
33847512958
-
-
note
-
1H NMR of the authentic starting material sample, indicating that no racemization occurred during the hydrolysis.
-
-
-
-
50
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0000951044
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(c) Hughes, D. L.; Reamer, R. A.; Bergan, J. J.; Grabowski, E. J. J. J. Am. Chem. Soc. 1988, 110, 6487.
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51
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0009071150
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PCT Int. Appl. 9603430, 1996
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Oberhauser, B.4
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52
-
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33646959585
-
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note
-
10 requires 1141.5678).
-
-
-
-
54
-
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33646961207
-
-
Details of the preparation may be found in the Supporting Information
-
Details of the preparation may be found in the Supporting Information.
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