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• W2080371922 endingPage "242" @default.
• W2080371922 startingPage "239" @default.
• W2080371922 abstract "A straightforward approach to enantiomerically enriched (R) and (S)-3-hydroxycyclopentanone is described. The key step involves a kinetic resolution of racemic 3-hydroxycyclopentanone using commercial Pseudomonas cepacia lipase immobilized on diatomite (Amano lipase PS-DI). The absolute stereochemistry of the product was determined by derivatization into (R)-3-(benzyloxy)cyclopentanone." @default.
• W2080371922 created "2016-06-24" @default.
• W2080371922 creator A5035234231 @default.
• W2080371922 creator A5059728580 @default.
• W2080371922 date "2013-01-01" @default.
• W2080371922 modified "2023-10-16" @default.
• W2080371922 title "Enantioselective preparation of (R) and (S)-3-hydroxycyclopentanone by kinetic resolution" @default.
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• W2080371922 doi "https://doi.org/10.1016/j.molcatb.2012.09.015" @default.
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