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- W2000766664 abstract "A preferential consumption of the (1S,2S) enantiomer of (±)-trans-,1-phenylpropene oxide (3) and of the (1R,2S) enantiomer of cis-1-phenylpropene oxide (5) is observed during the rabbit liver mEH catalyzed hydrolysis of these epoxides. This preference is, respectively, much lower and much higher than that found for the consumption of the (R) enantiomer in the hydrolysis of (±)-styrene oxide. These results are rationalized in terms of the KM and Vmax of the respective reactions." @default.
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- W2000766664 date "1993-06-01" @default.
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- W2000766664 title "Substrate enantioselectivity m the rabbit liver microsomal epoxide hydrolase catalyzed hydrolysis of trans and cis 1-phenylpropene oxides. A comparison with styrene oxide" @default.
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- W2000766664 doi "https://doi.org/10.1016/s0957-4166(00)80222-0" @default.
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