Convenient synthesis of stereospecifically deuteriated glycines from glutamic acid using a combination of enzymatic and chemical methods
Abstract
Chiral glycines (1a) and (1b) have been synthesized starting from stereospecifically deuteriated 4-aminobutanoic acids (3a) and (3b). Enzymatic decarboxylation of (2S)-glutamic acid (2a) in 2H2O and (2R,S)-[2,4,4-2H3]glutamic acid (2b)+(2c) in H2O afforded (3a) and (3b), respectively. Chemical transformations of deuteriated pyrrolidinones (4a) and (4b) afforded stereospecifically labelled glycines (1a) and (1b) in good yields.