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Updated: Jul 6, 2026

Light-driven Enzymatic Decarboxylation
Published on: May 22, 2016
Catalytic oxidation of organic substrates by molecular oxygen and hydrogen peroxide by multistep electron transfer--a
1Department of Organic Chemistry, Arrhenius Laboratory, Stockholm University, Stockholm, Sweden.
Abstract:
Oxidation reactions are of fundamental importance in nature, and are key transformations in organic synthesis. The development of new processes that employ transition metals as substrate-selective catalysts and stoichiometric environmentally friendly oxidants, such as molecular oxygen or hydrogen peroxide, is one of the most important goals in oxidation chemistry. Direct oxidation of the catalyst by molecular oxygen or hydrogen peroxide is often kinetically unfavored. The use of coupled catalytic systems with electron-transfer mediators (ETMs) usually facilitates the procedures by transporting the electrons from the catalyst to the oxidant along a low-energy pathway, thereby increasing the efficiency of the oxidation and thus complementing the direct oxidation reactions. As a result of the similarities with biological systems, this can be dubbed a biomimetic approach.
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