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- W2620172918 startingPage "4542" @default.
- W2620172918 abstract "Metal-free enantiocomplementary hydrolytic dynamic kinetic resolution of Morita–Baylis–Hillman (MBH) acetates was developed using triethylamine (TEA) as a racemization catalyst and wild-type or engineered lipase B from Candida antarctica (CALB) as stereoselectivity-determining catalyst, leading to chiral MBH alcohols with tailor-made R or S configurations on an optional basis. In the TEA-WT CALB catalysis system, WT CALB displays excellent S enantioselectivity for a series of MBH acetates tested (up to 96% ee and 98% conversion). Reversal of enantioselectivity in favor of (R)-MBH alcohols (95% ee; 95% conversion) was achieved by generating a focused site-specific mutagenesis library composed of less than 20 variants. Molecular modeling explains the origin of stereoselectivity." @default.
- W2620172918 created "2017-06-05" @default.
- W2620172918 creator A5015800814 @default.
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- W2620172918 creator A5035749492 @default.
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- W2620172918 creator A5057455449 @default.
- W2620172918 creator A5070504336 @default.
- W2620172918 creator A5076203174 @default.
- W2620172918 date "2017-06-08" @default.
- W2620172918 modified "2023-09-30" @default.
- W2620172918 title "Stereoselectivity-Tailored, Metal-Free Hydrolytic Dynamic Kinetic Resolution of Morita–Baylis–Hillman Acetates Using an Engineered Lipase–Organic Base Cocatalyst" @default.
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