New high-epoxy vegetable oils from nine species representing three plant families and four genera have been investigated. The epoxyacyl moiety in at least one oil from each genus was characterized and shown to be the (+)-vernoloyl (cis-12,13-epoxy-cis-9-octadecenoyl) group. Intraglyceride distribution studies revealed a general preference of the (+)-vernoloyl groups for the beta-position of triglyceride molecules. Interglyceride distribution of (+)-vernoloyl groups was studied in three oils and found not to agree with predictions based on either 1,2,3-random or 1,3-random-2-random distribution. A striking exception to the general intraglyceride distribution pattern was discovered in the monoepoxy triglyceride fraction fromEuphorbia lagascae seed oil.
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http://dx.doi.org/10.1007/BF02532677 | DOI Listing |
Lipids
September 1968
Northern Regional Research Laboratory, 61604, Illinois, Peoria.
Coriolic [(R)-13-hydroxy-cis-9,trans-11-octadecadienoic] acid (III, R=Z=H) was isolated as the methyl ester from twoCoriaria seed oils in 66 and 68% yields. The double bonds and hydroxyl group were located by periodate-permanganate oxidation before, and chromic acid oxidation after, hydrogenation of the double bonds. Alternatively the positions of the functional groups were indicated by a convenient micro-ozonolysis-gas-liquid chromatographic procedure.
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September 1966
Northern Regional Research Laboratory, Peoria, Illinois.
New high-epoxy vegetable oils from nine species representing three plant families and four genera have been investigated. The epoxyacyl moiety in at least one oil from each genus was characterized and shown to be the (+)-vernoloyl (cis-12,13-epoxy-cis-9-octadecenoyl) group. Intraglyceride distribution studies revealed a general preference of the (+)-vernoloyl groups for the beta-position of triglyceride molecules.
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