Abstract
Lipase from Candida cylindracea was used to catalyze the enantioselective esterification in isooctane to resolve naproxen. The conversion was 33.5% over 11 days. The enantiomer excess of product (ee %) was about 100% at this conversion when octanol acted as the other substrate.
Similar content being viewed by others
References
Battistel, E., Bianchi, D., Cesti, P. and Pina, C. (1991) Biotechnol. and Bioeng. 38, 659–664.
Belan, A., Bolte, G. and Fauve, A. (1987) J. Org. Chem. 52, 256–260.
Gupta, M.N. (1992) Eur. J. Biochem. 203, 25–32.
Harrison, I. T., Lewis, B, Nelson, P., Rooks, W. et al. (1987) J. Am. Chem. Soc. 109, 7122.
Linko, Y. Y., Wang, Z. L. and Seppala, J. (1994) Biocatalysis,8, 269–282.
Martins, J. F., Sampio, T. C., Carvalho, I. B. and Barreiros, S. (1994) Biotechnol. and Bioeng. 44, 119–124.
Zaks A, and Klibanov A. M. (1988) J. Biol. Chem. 263, 3194.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Cui, Ym., Wei, Dz. & Yu, Jt. Lipase-catalyzed esterification in organic solvent to resolve racemic naproxen. Biotechnology Letters 19, 865–868 (1997). https://doi.org/10.1023/A:1018333503317
Issue Date:
DOI: https://doi.org/10.1023/A:1018333503317