Reactions of 5α-hydroxy steroids : IX. T
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J.M. Coxon; M.P. Hartshorn
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Article
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1969
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Elsevier Science
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French
⚖ 203 KB
The Westphalen rearrangement' of 38,68-substituted-cholestan-5u-ols (1) to give 5g-methyl-A'-compounds (2) has received considerable study2. No rearrangement products are obtained from 5J3-hydroxy-3, 6a-substituted-4, 6f3-methyl-5 or 6-keto-derivatives 6 . Recently Davies and Summers' reported t