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• W1992085124 abstract "Starting from easily available ethyl 2-methyl-4,4,4-trifluoroacetoacetate and benzylamine each of the four stereoisomers of α-methyl-β-trifluoromethyl-β-alanine have been synthesized in optically pure form via stereocontrolled chemo-enzymatic procedure including diastereoselective base-catalyzed [1,3]-proton shift reaction and enantioselective penicillin acylase-catalyzed resolution." @default.
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• W1992085124 date "1994-07-01" @default.
• W1992085124 modified "2023-10-08" @default.
• W1992085124 title "Chemo-enzymatic approach to the synthesis of each of the four isomers of α-alkyl-β-fluoroalkyl-substituted β-amino acids" @default.
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• W1992085124 doi "https://doi.org/10.1016/0957-4166(94)80163-0" @default.
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