Long chain 3-O-acylcatechins were prepared in high yield by alcoholysis wit
h n-butanol of the corresponding pentaacylderivatives in the presence of li
pase from Mucor miehei (immobilised, Lipozyme(R) IM). In an alternative pro
cedure, the mixed ester, tetraacetyl-3-O-acylcatechin, was synthesised and
used as substrate for the same alcoholysis process that proceeds with highe
r reaction rate. The obtained 3-O-acyl derivatives are more lipophilic than
the parent catechin and thus suitable for a possible application of their
antioxidative properties in hydrophobic matrices. (C) 2000 Elsevier Science
B.V. All rights reserved.