cis-trans isomerization of unsaturated fatty acids withp-toluenesulfinic acid View Full Text


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Article Info

DATE

1982-11

AUTHORS

J. M. Snyder, C. R. Scholfield

ABSTRACT

Elaidination of unsaturated fatty acids usingp-toluenesulfinic acid yielded 77–80% totaltrans unsaturation in the products. Results from reactions with monoene, diene, and triene isomers indicated that only geometric isomerization takes place. Each double bond isomerized randomly and independently in the polyunsaturated fatty acids. Reactions proceeded quickly, and the method proved convenient and reliable. More... »

PAGES

469-470

References to SciGraph publications

  • 1966-05. Preparation of pure methyl esters by counter double current distribution in LIPIDS
  • 1964-06. Preparation of 9,15-octadecadienoate isomers1 in JOURNAL OF THE AMERICAN OIL CHEMISTS' SOCIETY
  • 1963-10. Cis-trans isomerization of oleic, linoleic and linolenic acids in JOURNAL OF THE AMERICAN OIL CHEMISTS' SOCIETY
  • 1978-05. Double bond analysis of dienoic fatty acids in mixtures in JOURNAL OF THE AMERICAN OIL CHEMISTS' SOCIETY
  • 1981-06. Gas chromatographic equivalent chain lengths of fatty acid methyl esters on a silar 10C glass capillary column in JOURNAL OF THE AMERICAN OIL CHEMISTS' SOCIETY
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    URI

    http://scigraph.springernature.com/pub.10.1007/bf02636144

    DOI

    http://dx.doi.org/10.1007/bf02636144

    DIMENSIONS

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