Related Experiment Video
Updated: Aug 19, 2026

Enzymatic Synthesis of Epoxidized Metabolites of Docosahexaenoic, Eicosapentaenoic, and Arachidonic Acids
Published on: June 28, 2019
iPF2alpha-III-17,18,19,20-d4: total synthesis and metabolism
Seongjin Kim1, William S Powell, John A Lawson
1Claude Pepper Institute and Department of Chemistry, Florida Institute of Technology, 150 West University Boulevard, Melbourne, FL 32901, USA.
Abstract:
The first total synthesis of 17,18,19,20-d4-iPF2alpha-III 32, a deuterated analog of iPF2alpha-III, is described. We have used this analog in some beta-oxidation studies with rat liver homogenates and have shown that 32 was metabolized to 17,18,19,20-tetradeutero-2,3-dinor-iPF2alpha-III 36 and 17,18,19,20-tetradeutero-2,3-dinor-5,6-dihydro-iPF2alpha-III 37.
Related Concept Videos
Production of Pharmaceuticals
Preparation of 1° Amines: Hofmann and Curtius Rearrangement Overview
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
