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Chemoenzymatic Synthesis of (R)- and (S)-4-Amino-3-Methylbutanoic Acids
Authors:Ryszard Andruszkiewicz  Anthony G. M. Barrett  Richard B. Silverman
Affiliation:1. Department of Chemistry and Department of Biochemistry , Molecular Biology, and Cell Biology, Northwestern University , Evanston, IL, 60208-3113;2. Department of Chemistry
Abstract:(R)- and (S)-4-Amino-3-methylbutanoic acids were synthesized in high yields via initial enantioselective hydrolysis of dimethyl 3-methylglutarate to methyl (R)-3-methylglutarate with pig liver esterase. The ester group was converted to an amine to give (R)-4-amino-3-methylbutanoic acid; the carboxylic acid was converted to an amine to give (S)-4-amino-3-methylbutanoic acid.
Keywords:Ring‐expanded  Tiazofurin  2′,3′‐Dideoxynucleoside  C‐Nucleosides  Synthesis  Conformation
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