Issue 13, 2024

Glyoxalase-based toolbox for the enantioselective synthesis of α-hydroxy carboxylic acids

Abstract

We report highly enantioselective synthesis of L-α-hydroxy carboxylic acids (L-αHCAs) via enzymatic intramolecular Cannizzaro reaction of (hetero)aryl glyoxals in the presence of glutathione-independent human glyoxalase DJ-1. Combined with the optimized synthesis of D-αHCAs using glyoxalases I and II, this approach offers a general, scalable and operationally simple access to both enantiomers of α-hydroxy acids in moderate to excellent yields with uniformly high enantioselectivity.

Graphical abstract: Glyoxalase-based toolbox for the enantioselective synthesis of α-hydroxy carboxylic acids

Supplementary files

Article information

Article type
Communication
Submitted
24 Dec 2023
Accepted
08 Feb 2024
First published
09 Feb 2024

Org. Biomol. Chem., 2024,22, 2539-2543

Glyoxalase-based toolbox for the enantioselective synthesis of α-hydroxy carboxylic acids

M. Yedigenov, N. Amire, A. Abdirassil, T. Mulikova, A. Begenov, A. Kiesilä, A. A. Peshkov, V. A. Peshkov and D. Utepbergenov, Org. Biomol. Chem., 2024, 22, 2539 DOI: 10.1039/D3OB02098C

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