In an effort to improve the chain-breaking capacity of the natural antioxidants, an octyltelluro group was introduced next to the phenolic moiety in β- and δ-tocopherol. The new vitamin E analogues quenched peroxyl radicals more efficiently than α-tocopherol and were readily regenerable by aqueous N-acetylcysteine in a simple membrane model composed of a stirring chlorobenzene/water two-phase system. The novel tocopherol analogues could also mimic the action of the glutathione peroxidase enzymes. © 2013 American Chemical Society.
CITATION STYLE
Singh, V. P., Poon, J. F., & Engman, L. (2013). Catalytic antioxidants: Regenerable tellurium analogues of vitamin e. Organic Letters, 15(24), 6274–6277. https://doi.org/10.1021/ol403131t
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