Synthesis of Enantiopure Drugs and Drug Intermediates by Immobilized Lipase-Catalysis
Jana Brabcova, Marco Filice, Melissa Gutarra and Jose M. Palomo
Pages 113-136 (24)
Enantiomerically pure product synthesis plays a key role in production of pharmaceuticals. The application of
biocatalytic approaches represents a convenient and sustainable way for this purpose. The enormous potential of enzymes
for the transformation of synthetic chemicals with high chemo-, regio- and enantioselectivity is on increasing awareness.
In particular, lipases show a high versatility to recognize non-natural substrates being successfully applied in regio- and
stereoselective biotransformations. The immobilization technology on lipases is not only a requisite for the industrial implementation
but it has been a great methodology to alter their catalytic properties to obtain highly enantio- and regioselective
biocatalysts in the enantioselective synthesis of chiral drugs or drug intermediates. This review focuses on showing
some of the latest advances on the use of immobilized lipases on pharmaceutical biotransformations.
Lipases, kinetic resolution, asymmetric transformation, chemical modification, immobilization, pharmaceuticals,
Departamento de Biocatalisis, Instituto de Catálisis (CSIC), Campus UAM Cantoblanco, 28049 Madrid, Spain.