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Dimeric epoxy fatty acid methyl esters: formation, chromatography and mass spectrometry

โœ Scribed by J. Gilbert; M.J. Shepherd; J.R. Startin; J. Eagles


Publisher
Elsevier Science
Year
1981
Tongue
English
Weight
324 KB
Volume
28
Category
Article
ISSN
0009-3084

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โœฆ Synopsis


The formation of dimers is reported from the thermal treatment of a series of epoxy fatty acid methyl esters. These compounds were isolated from the reaction mixture by steric exclusion chromatography and were subsequently characterised by their high resolution electron impact and ammonia chemical ionisation mass spectra. The spectra were consistent in each case with the presence of a mixture of four possible positional isomers each containing an ether bridge linking a pair of fatty acid methyl esters across the carbon chains, with a keto group on a carbon adjacent to the bridge on one of the esters.


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Liquid chromatography/mass spectrometry
โœ J. D. Baty; R. G. Willis; R. Tavendale ๐Ÿ“‚ Article ๐Ÿ“… 1985 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 347 KB ๐Ÿ‘ 1 views

The mass spectra of a series of saturated and unsaturated fatty acids have been recorded as their anthrylmethyl esters using a liquid chromatographic mass spectrometric interface. The spectra show an intense peak for the aromatic nucleus, and a molecular ion. The liquid chromatographichnass spectrom