Abstract
The redox behavior of "active aldehydes" 1- derived from 3-benzylthiazolium salts and simple aldehydes in the presence of a base has been examined with low-temperature cyclic voltammetry and EPR spectroscopy. The highly negative oxidation potentials of 1- and the spin distribution of the intermediate radicals 1. indicate that the active aldehyde can act as an efficient electron mediator in thiamin-dependent enzymatic redox systems.
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