Add time:08/30/2019         Source:sciencedirect.com

Reduction of 3β-benzoyloxy-cholest-8(14)-en 13-one with lithium aluminum hydride yielded two epimers (at C-15) of cholest-8(14)-en-3β,15-diol. Reduction with lithium aluminum tritide yielded [15α-3H]-cholest-8(14)-en-3β,15β-diol and [15β-3H]-cholest-8(14)-en-3β,155-diol. Both labeled compounds served as efficient substrates for cholesterol formation in rat liver homogenate preparations.

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