Application of Chemoenzymatic Hydrolysis in the Synthesis of 2-Monoacylglycerols
- PMID: 22822273
- PMCID: PMC3398708
- DOI: 10.1016/j.tet.2012.04.101
Application of Chemoenzymatic Hydrolysis in the Synthesis of 2-Monoacylglycerols
Abstract
The selective biocatalyzed synthesis of 2-monoacylglycerols (2-MAGs) through the use of commercially available immobilized Candida antarctica (Novozym435) and Rhizomucor miehei is explored. Reactions at room temperature result in the formation of a 2-MAG and a corresponding ethyl ester of the fatty acid with immobilized Candida antarctica within 2h with yields ranging from 36%-83%. Similar reaction conditions with immobilized Rhizomucor miehei yielded exclusively the 2-MAG after 24h with yields ranging from 37% to 88%. Yields vary on the acyl group at the sn-2 position and choice of enzyme involved.
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