Cu-Catalyzed Tandem Oxidation-Intramolecular Cannizzaro Reaction of Biorenewables and Bioactive Molecules.
Hristo PetkovMartin A RavutsovManuel J VerganistaYavor N MitrevNuno R CandeiasSvilen P SimeonovPublished in: ChemSusChem (2024)
A tandem Cu-catalyzed oxidation-intramolecular Cannizzaro reaction leading to bioactive α-hydroxyesters from α-hydroxyketones is reported. The process uses oxygen as a sole oxidant to achieve the formation of glyoxals, which are efficiently converted in situ to important α-hydroxyesters. The mechanistic insights are provided by isotopic labeling and supported by DFT calculations. The transformation proved a robust synthetic tool to achieve the synthesis of human metabolites and hydroxyl esters of various biologically active steroid derivatives.
Keyphrases
- electron transfer
- density functional theory
- room temperature
- endothelial cells
- hydrogen peroxide
- energy transfer
- molecular dynamics
- aqueous solution
- ms ms
- induced pluripotent stem cells
- molecular dynamics simulations
- metal organic framework
- molecular docking
- visible light
- nitric oxide
- anti inflammatory
- ionic liquid
- structure activity relationship