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- W2042154265 abstract "Lipase QL (from Alcaligenes sp.)-catalyzed acylation of alcohols using isopropenyl acetate as the acylating agent in diisopropyl ether converted preferentially primary alcohols with an S configuration and secondary alcohols with an R configuration into the corresponding homochiral acetates. On the basis of observed enantiomer selectivities, a predictive active site model for lipase QL is proposed for identifying which enantiomer of a primary or a secondary alcohol reacts faster in this acylation." @default.
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- W2042154265 date "1996-11-01" @default.
- W2042154265 modified "2023-10-18" @default.
- W2042154265 title "Enantioselective acylation of primary and secondary alcohols catalyzed by lipase QL from Alcaligenes sp.: A predictive active site model for lipase QL to identify which enantiomer of an alcohol reacts faster in this acylation" @default.
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- W2042154265 doi "https://doi.org/10.1016/0957-4166(96)00429-6" @default.
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