We have previously demonstrated an efficient polyester synthesis of omega-hydroxyacids catalysed by the Candida rugosa lipase in dry hexane (1,2). This method is now extended to the polymerisation of racemic 10-hydroxyundecanoic acid to explore the polymerisation of a secondary alcohol and the ability of the lipase to display stereoselectivity, The resultant polyester (similar to 1000 Mwt) contained monomer units with an average enantiomeric excess of 60%ee favouring the (S) enantiomer. The residual monomer was recovered with a 33%ee favouring the (R) enantiomer. The origin of this stereoselectivity has been evaluated and it has been shown to arise due to the immediate chiral environment surrounding the esterification event between the acylated enzyme and the secondary alcohol nucleophile. It is not due to recognition of the remote secondary alcohol functional group by the enzyme during initial acylation.