Issue 1, 1994

Stereoelectronic influence of fluorine in enzyme resolutions of α-fluoroesters

Abstract

The very high enantioselectivity demonstrated by two different lipase enzymes towards α-fluoroesters is shown from quantitative PM3 and ab initio 6-31G* SCF-MO calculations to arise from stereoelectronic factors, which are predicted to be reduced when the diastereoisomeric transition states are modelled in the condensed aqueous phase.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1994, 3-4

Stereoelectronic influence of fluorine in enzyme resolutions of α-fluoroesters

D. O'Hagan and H. S. Rzepa, J. Chem. Soc., Perkin Trans. 2, 1994, 3 DOI: 10.1039/P29940000003

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