An enantioselective synthesis of the structure reported for the natural antifungal compound,(−)-crassinervic acid (1), has been achieved starting from geraniol and p- hydroxybenzoic acid. The key chirality-inducing step is a Sharpless asymmetric epoxidation of an allylic alcohol, on the basis of which the S configuration can be assigned to the (−) natural enantiomer. The discrepancies between the spectroscopic data for synthetic and ...