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• W2203986730 abstract "The synthesis of optically active 3-hydroxyalkanoates of varying chain length (Clo, C14 and C18) was investigated using chemoenzymatic methods. While bakers' yeast mediated reduction of 3-oxoalkanoates gave (R)-3-hydroxyalkanoates (e.e. >80%, yield —10%), both enantiomers were obtained by enzymatic resolution of racemic methyl 3-butanoyloxyalkanoates using Geotrichum candidum lipase with moderate to good optical purity (e.e. 32–92%, yield 40–60% for both enantiomers). Lipase-catalysed interesterification, however, was found to proceed with similar enantioselectivity but with slow rate of conversion." @default.
• W2203986730 created "2016-06-24" @default.
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• W2203986730 date "1990-01-01" @default.
• W2203986730 modified "2023-10-17" @default.
• W2203986730 title "Chemoenzymatic Preparation of Optically Active Long-Chain 3-Hydroxyalkanoates" @default.
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• W2203986730 doi "https://doi.org/10.3109/10242429008992057" @default.
• W2203986730 hasPublicationYear "1990" @default.
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