Synthesis and isolation of trans-7, cis-9 octadecadienoic acid and other CLA isomers by base conjugation of partially hydrogenated γ-linolenic acid
Author:
Publisher
Wiley
Subject
Cell Biology,Organic Chemistry,Biochemistry
Reference20 articles.
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2. Davis, A.L., McNeill, G.P., and Caswell, D.C. (1999) Analysis of Conjugated Linoleic Acid Isomers by 13C NMR Spectroscopy, Chem. Phys. Lipids 97, 155–165.
3. Yurawecz, M.P., Hood, J.K., Roach, J.A.G., Mossoba, M.M., Daniels, D.H., Ku, Y., Pariza, M.W., and Chin, S.F. (1994) Conversion of Allylic Hydroxy Oleate to Conjugated Linoleic Acid and Methoxy Oleate by Acid-Catalyzed Methylation Procedures, J. Am. Oil Chem. Soc. 71, 1149–1155.
4. Yurawecz, M.P., Roach, J.A.G., Sehat, N., Mossoba, M.M., Kramer, J.K.G., Fritsche, J., and Steinhart, H. (1998) A New Conjugated Linoleic Acid (CLA) Isomer, 7-trans,9-cis-Octadecadienoic Acid in Cow Milk, Cheese, Beef, and Human Milk and Adipose Tissue, Lipids 33, 803–809.
5. Park, Y., Storkson, J.M., Albright, K.J., Liu, W., and Pariza, M.W. (1999) Evidence That the Trans-10,cis-12 Isomer of Conjugated Linoleic Acid Induces Body Composition Changes in Mice, Lipids 34, 235–241.
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