ThDP-dependent enzyme catalyzed oxidation of aldehydes

Abstract

Natural thiamine diphosphate (ThDP)-dependent enzymes are frequently utilized to catalyze the decarboxylation of β-keto acids and the benzoin condensation of aldehydes. Herein, we present a ThDP-dependent enzymatic oxidation of aldehydes mediated by sequential single electron transfer (SET) processes, utilizing hexachloroethane (C2Cl6) as the oxidant. The reaction exhibits high efficiency (yield up to 99% and turnover number up to 2000) and achieves effective stereoselective control for dynamic kinetic resolutions (e.e. up to 99%). This study uncovers a previously undiscovered capability of ThDP-dependent enzymes, thus broadening the functional repertoire of this enzyme class.

Graphical abstract: ThDP-dependent enzyme catalyzed oxidation of aldehydes

Supplementary files

Article information

Article type
Edge Article
Submitted
05 May 2025
Accepted
05 Aug 2025
First published
06 Aug 2025
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2025, Advance Article

ThDP-dependent enzyme catalyzed oxidation of aldehydes

X. Chen, M. Zhou, X. Duan, Y. Zhang, X. Chu and J. Xu, Chem. Sci., 2025, Advance Article , DOI: 10.1039/D5SC03250D

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements