ChemInform Abstract: Asymmetric Synthesis via Acetal Templates. Part 15. The Preparation of Enantiomerically Pure Mevinolin Analogues.
ChemInform Abstract
The key step in the synthesis of the chiral δ-lactones (V) is the titanium tetrachloride promoted reaction of the cyclic acetals (I) with the bis(siloxy)methoxybutadiene (II), yielding the δ-alkoxy-β-keto esters (III).