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- W2012586488 abstract "Abstract The long-chain moieties in positions 1, 2 and 3 of the 1-alk-1'-enyl 2,3-diacyl sn-glycerols and 1 alkyl 2,3-diacyl sn-glycerols of raffish (Hydrolagus colliei) liver were analyzed. In both classes of neutral alkoxylipids, the 2-acyl moieties are free of branched chains, although the 3-acyl moieties, the I-alkyl moieties and, especially, the 1-alk-1'-enyl moieties contain branched isomers. The 1,2-disubstituted glycerols derived from the neutral alkoxylipids were analyzed as acetates by argentation chromatography and gas chromatography. The predominant molecular species of the 1-alk-1'-enyl 2-acyl sn-glycerols are different from those of the 1-alky1 2-acyl s%-glycerols. Thus, direct interconversions of alk-1-enyl and alkyl moieties, or between the two classes of neutral alkoxylipids, appear unlikely." @default.
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- W2012586488 date "1970-05-01" @default.
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- W2012586488 title "Alkoxylipids VI. Molecular structures of the neutral alkoxylipids of ratfish liver" @default.
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- W2012586488 doi "https://doi.org/10.1016/0005-2760(70)90117-7" @default.
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