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- W2022245684 abstract "Lipase-catalyzed transesterifications of aryl-substituted alcohols with vinyl acetate in organic solvents have been investigated. Vmax of (R)-1-phenylethanol is much larger than its (S)-counterpart, although their Kms are similar each other. It is proposed that a lipase from Pseudomonas cepacia can form a complex easily with each enantiomer, although the complex with the (S)-enantiomer is abortive. Enantioselectivity for the ortho-substituted 1-phenylethanol is smaller than those for the others. A three-dimensional model for the active domain of the lipase has been proposed to explain the enantioselectivity and substrate selectivity of the lipase." @default.
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- W2022245684 date "1996-04-01" @default.
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- W2022245684 title "Lipase-Catalyzed Transesterification of Aryl-Substituted Alkanols in an Organic Solvent" @default.
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- W2022245684 doi "https://doi.org/10.1246/bcsj.69.1079" @default.
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