Directed sequential synthesis of conjugated linoleic acid isomers from Δ 7, 9 to Δ 12, 14-Reference-Cited by-同舟云学术

Directed sequential synthesis of conjugated linoleic acid isomers from Δ 7, 9 to Δ 12, 14

Published:2003-01 Issue:1 Volume:105 Page:3-8
ISSN:1438-7697
Container-title:European Journal of Lipid Science and Technology
language:en
Short-container-title:Eur. J. Lipid Sci. Technol.

Author:

Destaillats Frédéric¹,Angers Paul¹

Affiliation:

1. Department of Food Science and Nutrition, and Dairy Research Center (STELA), Université Laval, Sainte Foy, Québec, Canada

Publisher

Wiley

Subject

Industrial and Manufacturing Engineering,General Chemistry,Food Science,Biotechnology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejlt.200390004

Reference32 articles.

1. M. E. Turini J. C. Martin:Sources functions and analysis of conjugated linoleic acid and its metabolites. In: Structured and modified lipids. Ed.F. D. Gunstone Marcel Dekker New York (USA) 2001 pp. 251‐284.

2. Free Radical Scavenging Properties of Conjugated Linoleic Acids

3. Furan fatty acids determined as oxidation products of conjugated octadecadienoic acid

4. Hydroperoxide formation during autoxidation of conjugated linoleic acid methyl ester

5. trans-10,cis-12-Conjugated Linoleic Acid Isomer Exhibits Stronger Oxyradical Scavenging Capacity than cis-9,trans-11-Conjugated Linoleic Acid Isomer

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