Kinetic resolution of α-lipoic acid, a case of remote stereocenter discrimination, was accomplished using lipase from Aspergillus oryzae WZ007. Performance of this lipase was investigated for enantioselective esterification of (S)-α-lipoic acid, leaving the target product (R)-α-lipoic acid in unreacted form. The effects of chain length of alcohol, type of solvent, molar ratio of alcohol:acid, and reaction temperature were studied. The optimum reaction conditions were found to be esterification with n-octanol at 50°C in heptane with an alcohol:acid molar ratio of 5:1. The conversion rate of α-lipoic acid was 75.2%, with an enantiomeric excess of 92.5% towards unreacted substrate in a reaction time of 48 h. © 2009 Society for Industrial Microbiology.
CITATION STYLE
Yan, H. D., Wang, Z., & Chen, L. J. (2009). Kinetic resolution of α-lipoic acid via enzymatic differentiation of a remote stereocenter. Journal of Industrial Microbiology and Biotechnology, 36(5), 643–648. https://doi.org/10.1007/s10295-009-0531-1
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