Conformational free energy differences in steroids. Part V. Equilibration of 5α- and 5β-androstan-6-one derivatives structurally modified in ring D
Abstract
The presence of 17β-groups (methoxy-, acetoxy-, ethyl, or 1,5-dimethylhexyl) or of unsaturation in ring D had little effect upon the position of equilibrium between substituted 5α- and 5β-androstan-6-ones.
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