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1 indicating that the C(17) hydroxyl is positioned to direct the epoxidation.
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0025058974
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Desilylation of (-)-10 and acetonide formation permitted confirmation of the stereochemistry via Rychnovsky-Evans acetonide analysis. See: (a) Rychnovsky, S. D.; Skalitzky, D. J. Tetrahedron Lett. 1990, 31, 945. (b) Rychnovsky, S. D.; Rogers, B.; Yang, G. J. Org. Chem. 1993, 58, 3511. (c) Evans, D. A.; Rieger, D. L.; Gage, J. R. Tetrahedron Lett. 1990, 31, 7099.
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33751385878
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Desilylation of (-)-10 and acetonide formation permitted confirmation of the stereochemistry via Rychnovsky-Evans acetonide analysis. See: (a) Rychnovsky, S. D.; Skalitzky, D. J. Tetrahedron Lett. 1990, 31, 945. (b) Rychnovsky, S. D.; Rogers, B.; Yang, G. J. Org. Chem. 1993, 58, 3511. (c) Evans, D. A.; Rieger, D. L.; Gage, J. R. Tetrahedron Lett. 1990, 31, 7099.
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19
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0025608552
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Desilylation of (-)-10 and acetonide formation permitted confirmation of the stereochemistry via Rychnovsky-Evans acetonide analysis. See: (a) Rychnovsky, S. D.; Skalitzky, D. J. Tetrahedron Lett. 1990, 31, 945. (b) Rychnovsky, S. D.; Rogers, B.; Yang, G. J. Org. Chem. 1993, 58, 3511. (c) Evans, D. A.; Rieger, D. L.; Gage, J. R. Tetrahedron Lett. 1990, 31, 7099.
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0012386243
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note
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The delicate nature of this intermediate was demonstrated by the requirement to carry the transformation to only partial conversion [i.e., % based on recovered starting material (BORSM)] followed by recyclization.
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