Literature DB >> 5637423

New method for the reductive ozonolysis of double bonds in monoenoic fatty acid methyl esters.

S Ramachandran, P V Rao, D G Cornwell.   

Abstract

Unsaturated methyl esters were cleaved to aldehydes and aldehydo-esters by ozonolysis followed by reduction with dimethyl sulfide after conversion to hydroperoxides. Cleavage products were identified by thin-layer chromatography and quantified by temperature programmed gas-liquid chromatography.

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Year:  1968        PMID: 5637423

Source DB:  PubMed          Journal:  J Lipid Res        ISSN: 0022-2275            Impact factor:   5.922


  3 in total

1.  Polyunsaturated fatty acids of skin; identification and 14 C-acetate incorporation.

Authors:  D I Wilkinson
Journal:  Lipids       Date:  1972-08       Impact factor: 1.880

2.  Cis-trans isomerization of unsaturated fatty acid methyl esters without double bond migration.

Authors:  D S Sgoutas; F A Kummerow
Journal:  Lipids       Date:  1969-07       Impact factor: 1.880

3.  Studies on the preparation and analysis of glyceryl ether derivatives and the isolation and reductive ozonolysis of unsaturated glyceryl ethers.

Authors:  S Ramachandran; H W Sprecher; D G Cornwell
Journal:  Lipids       Date:  1968-11       Impact factor: 1.880

  3 in total

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