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The process is initiated as described below by abstraction of a hydrogen atom from the central carbon of the pentadiene structure found in most fatty acid acyl chains containing more than one double bond: -CH = CH-CH 2 -CH = CH- -CH = CH-CH-CH = CH- + H Contrary to the native molecule, the lipid radical (L) reacts very quickly with atmospheric oxygen making a peroxy-radical (LOO) which again may abstract a hydrogen from another acyl chain resulting in a lipid hydroperoxide (LOOH) and a new radical L

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doi:10.1002/ptr.6646 Tian J, Liu Y, Chen K