Acyl radical cyclizations in synthesis. Part 3. Synthesis of (±)-trans-3,5-bis-(t-butyldimethylsiloxy)-2-methylenecyclohexanone, an ‘<scp>A</scp>’ ring model for 1α, 25-dihydroxyvitamin D₃

Abstract

A concise synthesis of (±)-trans-3,5-bis(t-butyldimethylsiloxy)-2-methylenecyclohexanone has been developed. The synthesis proceeds in seven steps from ethyl acetoacetate and involves a highly efficient acyl radical cyclization to construct the six-membered ring.