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• W2203350573 abstract "Abstract The dynamic kinetic resolution of α‐substituted racemic β‐lactams by alcoholytic ring‐opening, catalyzed by immobilized lipase B from Candida antarctica is described. With this process, a variety of racemic α‐substituted N ‐Cbz‐azetidinones (Cbz=benzyloxycarbonyl) was transformed to the corresponding N ‐Cbz‐protected β 2 ‐amino acid allyl esters with high enantioselectivity (up to 99%) and high yields (up to quantitative) at room temperature. magnified image" @default.
• W2203350573 created "2016-06-24" @default.
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• W2203350573 date "2015-12-17" @default.
• W2203350573 modified "2023-10-18" @default.
• W2203350573 title "Enantiopure<i>N</i>-Benzyloxycarbonyl-β²-amino Acid Allyl Esters from Racemic β-Lactams by Dynamic Kinetic Resolution using<i>Candida antarctica</i>Lipase B" @default.
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• W2203350573 doi "https://doi.org/10.1002/adsc.201500820" @default.
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