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Updated: Feb 27, 2026

Enzymatic Synthesis of Epoxidized Metabolites of Docosahexaenoic, Eicosapentaenoic, and Arachidonic Acids
Published on: June 28, 2019
A succinct access to ω-hydroxylated jasmonates via olefin metathesis
Guillermo H Jimenez-Aleman1, Selina Seçinti1, Wilhelm Boland1
1Department of Bioorganic Chemistry, Max Planck Institute for Chemical Ecology, 07745 Jena, Germany.
Abstract:
In higher plants, jasmonates are lipid-derived signaling molecules that control many physiological processes, including responses to abiotic stress, defenses against insects and pathogens, and development. Among jasmonates, ω-oxidized compounds form an important subfamily. The biological roles of these ω-modified derivatives are not fully understood, largely due to their limited availability. Herein, a brief (two-step), simple and efficient (>80% yield), versatile, gram-scalable, and environmentally friendly synthetic route to ω-oxidized jasmonates is described. The approach utilizes olefin cross-metathesis as the key step employing inexpensive, commercially available substrates and catalysts.
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