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 H 2O afforded (3a) and (3b), respectively. Chemical transformations of deuteriated pyrrolidinones (4a) and (4b) afforded stereospecifically labelled glycines (1a) and (1b) in good yields.

Convenient synthesis of stereospecifically deuteriated glycines from glutamic acid using a combination of enzymatic and chemical methods / E. Santaniello, R. Casati, A. Manzocchi. - In: JOURNAL OF THE CHEMICAL SOCIETY. PERKIN TRANSACTIONS. I. - ISSN 0300-922X. - :0(1985), pp. 2389-2392.

Convenient synthesis of stereospecifically deuteriated glycines from glutamic acid using a combination of enzymatic and chemical methods

E. Santaniello
Primo
;
A. Manzocchi
Ultimo
1985

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 H 2O afforded (3a) and (3b), respectively. Chemical transformations of deuteriated pyrrolidinones (4a) and (4b) afforded stereospecifically labelled glycines (1a) and (1b) in good yields.
Settore BIO/10 - Biochimica
1985
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/194557
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