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Thiamine-Based Enzymes for Biotransformations
Published Online: 15 JUL 2010
DOI: 10.1002/9783527628698.hgc028
Copyright © 2010 Wiley-VCH Verlag GmbH & Co. KGaA. All rights reserved.
Book Title

Handbook of Green Chemistry
Additional Information
How to Cite
Pohl, M., Gocke, D. and Müller, M. 2010. Thiamine-Based Enzymes for Biotransformations. Handbook of Green Chemistry. 3:75–114.
Publication History
- Published Online: 15 JUL 2010
- Abstract
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Chiral and prochiral
-oxyfunctionalized compounds, in particular carboxylic acids, aldehydes, ketones, alcohols, are indispensable building blocks for asymmetric synthesis. 2-Hydroxy ketones encompassing a chiral and prochiral center are therefore versatile building blocks for organic synthesis, as they can be easily transformed into other functionalities, such as diols, epoxides, amino alcohols and diamines. The review describes the current state of the art concerning thiamine diphosphate-dependent enzymes, which catalyze the formation of chiral 2-hydroxy ketones.
Keywords: thiamine; diphosphate; enzymes; biotransformation; carboligation; structurefunction relationships; pyruvate decarboxylase; benzoylformate decarboxylase; benzaldehyde lyase
