Related Experiment Video
Updated: Sep 16, 2025

Enzymatic Synthesis of Epoxidized Metabolites of Docosahexaenoic, Eicosapentaenoic, and Arachidonic Acids
Published on: June 28, 2019
Docosahexaenoic Acid Isomerized Through [1,5] and [1,3] Sigmatropic Rearrangements During Deodorization Process:
Linshang Zhang1, Zimu Li1, Hui Wang2
1College of Food Science and Engineering, Henan University of Technology, Zhengzhou, Henan, China.
Abstract:
The isomerization of docosahexaenoic acid (DHA) is intricate, leading to DHA loss during the industrial deodorization process. In this research, deodorization parameters of algae oil were optimized on a laboratory scale, with recommendations for temperature not exceeding 190°C and duration no longer than 70 min. The formation of conjugated trienes and dienes was confirmed by infrared spectrum and nuclear magnetic resonance analysis. To verify the formation process of conjugated trienes and dienes, density functional theory was employed. It was established that both [1,5] and [1,3] sigmatropic rearrangements transpired within this process. The [1,5] sigmatropic rearrangements exhibited lower activation energy than [1,3] counterparts, indicating that [1,5] sigmatropic rearrangements are more facile. This study validated the positional isomerization of DHA and offered valuable guidance for the algae oil production industry. PRACTICAL APPLICATION: This study examines how DHA levels decrease during the refining process of algal oil. It suggests a temperature threshold of 190°C and a processing time of 70 min to minimize this loss. These findings can guide improvements in algal oil refining and help consumers understand why DHA is lost during processing.
Related Concept Videos
Thermal Sigmatropic Reactions: Overview
Sigmatropic shifts are classified based on an order term [i, j ], where i and j indicate the number of atoms across which each end of the σ bond migrates. Below are examples of a [3,3] sigmatropic shift in...
[3,3] Sigmatropic Rearrangement of 1,5-Dienes: Cope Rearrangement
Stability of Conjugated Dienes
A comparison of the enthalpies of hydrogenation of dienes reveals that conjugated dienes release less heat on hydrogenation, rendering them more stable than their nonconjugated analogs.
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Preparation of Diols and Pinacol Rearrangement
The reaction begins with transferring a proton from the acid catalyst to one of the hydroxyl groups, producing an oxonium ion.
[3,3] Sigmatropic Rearrangement of Allyl Vinyl Ethers: Claisen Rearrangement

