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. Author manuscript; available in PMC: 2018 Feb 3.
Published in final edited form as: Biochem Biophys Res Commun. 2017 Feb 3;482(3):419–425. doi: 10.1016/j.bbrc.2016.10.086

Figure 1.

Figure 1

General mechanism for peroxidation of PUFAs. A hydrogen atom at a bisallylic position is remove using either a radical or a redox active metal to generate a resonance stabilized carbon centered radical. The double bonds of the acid isomerize to form the more thermodynamically stable conjugated diene prior to reacting with molecular oxygen.