AMBIENTUM BIOETHICA BIOLOGIA CHEMIA DIGITALIA DRAMATICA EDUCATIO ARTIS GYMNAST. ENGINEERING EPHEMERIDES EUROPAEA GEOGRAPHIA GEOLOGIA HISTORIA HISTORIA ARTIUM INFORMATICA IURISPRUDENTIA MATHEMATICA MUSICA NEGOTIA OECONOMICA PHILOLOGIA PHILOSOPHIA PHYSICA POLITICA PSYCHOLOGIA-PAEDAGOGIA SOCIOLOGIA THEOLOGIA CATHOLICA THEOLOGIA CATHOLICA LATIN THEOLOGIA GR.-CATH. VARAD THEOLOGIA ORTHODOXA THEOLOGIA REF. TRANSYLVAN
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Authors: BOTOND NAGY, MӐDӐLINA ELENA MOISӐ, ALINA FILIP, LÁSZLÓ CSABA BENCZE, MONICA IOANA TOȘA.
A series of commercially available lipases in various solvents using several alcohols as nucleophiles were studied for the stereoselective esterification of ibuprofen and alcoholysis of ibuprofen esters respectively. Novel methods were developed for the stereoselective synthesis of both enantiomers of the target compound. The (S)-selective alcoholysis and (R)-selective hydrolysis in a parallel kinetic resolution procedure in presence of lipase from Mucor miehei as catalyst were performed.
Keywords: lipase, Ibuprofen, enzymatic kinetic resolution, stereoselectivity
Published Online: 2016-12
