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- W2017693501 abstract "Primary alcohols having a hydroxymethyl group at an S stereogemic center and secondary alcohols with an R configuration are preferentially acylated to give the corresponding acetates by lipase YS (from Pseudomonas fluorescens)-catalyzed acylation using isopropenyl acetate as the acylating agent in diisopropyl ether. On the basis of enantiomer selectivities observed, a predictive active site model for lipase YS is proposed for identifying which enantiomer of a primary or a secondary alcohol reacts faster in this acylation." @default.
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- W2017693501 date "1995-09-01" @default.
- W2017693501 modified "2023-10-18" @default.
- W2017693501 title "Lipase-catalyzed enantioselective acylation of alcohols: a predictive active site model for lipase YS to identify which enantiomer of an alcohol reacts faster in this acylation" @default.
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- W2017693501 doi "https://doi.org/10.1016/0957-4166(95)00316-h" @default.
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