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The stereoselective synthesis of a set of four stable 5‐hydroxyeicosatetraenoic acid (HETE) analogues with a ferrocene backbone is described. The common substructure of all HETEs, the (2E,4Z)‐1‐hydroxyhexadiene moiety, was formally replaced by a ferrocenylmethanol fragment. Whereas the hydrophilic side chain remained the same as that of 5‐HETE (butyrate), the lipophilic side chain was simplified by...
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