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STEROIDVERBINDUNGEN XLIII. LITHIUM ALUMINIUM HYDRIDE REDUCTION OF 16α, 17α-OXIDO- 16β-METHYL-20-OXO-STEROID

Tsu‐Tzu Tsai

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Abstract

16α, 17α-Oxido-16β-methyl-△~5-pregnen-3β-ol-20-one (Ⅱ) was reduced to a mixture of compounds Ⅶa, Ⅷa and Ⅸa by lithium aluminium hydride. Structures of these compounds were proved by degradation reactions. The C_(20)-configurations were established by comparisons of relative reaction rates, molecular model consideration, and molecular rotation differences of the related compounds.

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16α, 17α-Oxido-16β-methyl-△~5-pregnen-3β-ol-20-one (Ⅱ) was reduced to a mixture of compounds Ⅶa, Ⅷa and Ⅸa by lithium aluminium hydride. Structures of these compounds were proved by degradation reactions. The C_(20)-configurations were established by comparisons of relative reaction rates, molecular model consideration, and molecular rotation differences of the related compounds.

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Available abstract

16α, 17α-Oxido-16β-methyl-△~5-pregnen-3β-ol-20-one (Ⅱ) was reduced to a mixture of compounds Ⅶa, Ⅷa and Ⅸa by lithium aluminium hydride. Structures of these compounds were proved by degradation reactions. The C_(20)-configurations were established by comparisons of relative reaction rates, molecular model consideration, and molecular rotation differences of the related compounds.

Key concepts: Chemistry, ALUMINUM HYDRIDE, Lithium aluminium hydride, Lithium (medication), Steroid, Aluminium, Hydride, Degradation (telecommunications)

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