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3-complexed carbonyl function preferentially from the axial site, i.e. the hindered β-face, to give mainly an α-trimethylsilyl ketone that resembled 10
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3-complexed carbonyl function preferentially from the axial site, i.e. the hindered β-face, to give mainly an α-trimethylsilyl ketone that resembled 10.
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33
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0011508727
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note
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2), 1.40 (1H, m, 9-H), 1.48 (1H, m, 20-H), 1.53 (1H, dd, J=12.2, 12.2 Hz, 1α-H), 1.59 (1H, m, 17-H), 1.63 (1H, m, 25-H), 1.69 (1H, m, 4β-H), 1.74 (1H, dd, J=12.2, 4.9 Hz, 1β-H), 1.79 (1H, m, 8-H), 1.87 (1H, ddd, J=15.1, 3.9, 3.4 Hz, 4α-H), 2.02 (1H, dd, J=13.2, 12.7 Hz, 7α-H), 2.29 (1H, dd, J=13.2, 4.4 Hz, 7β-H), 2.69 (1H, dd, J=12.7, 3.9 Hz, 5-H), 3.53 (1H, dd, J=8.8, 1.5 Hz, 22-H), 3.68 (1H, m, 2-H), 3.69 (1H, dd, J=8.8, 2.0 Hz, 23-H), 3.98 (1H, m, 3-H).
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36
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0029121205
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0011481160
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4 is corrected to 0.3% in this paper. Although this discrepancy remains to be accounted for, the later assay consistently gave ca. 0.3% activity, even when repeated three times
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4 is corrected to 0.3% in this paper. Although this discrepancy remains to be accounted for, the later assay consistently gave ca. 0.3% activity, even when repeated three times.
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39
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37049098489
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