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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 17 (1994), S. 308-311 
    ISSN: 0935-6304
    Keywords: Capillary GC ; Mass selective detection ; Multidimensional GC-MSD ; Fish oil ; Furan fatty acids ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The separation and analysis of furan fatty acids and other minor component fatty acids present at very low concentrations in complex sample matrices, such as fish oil or lipids derived from liver and testes, require several pre-analytical separation steps if single column gas chromatography is to furnish sufficient resolution: after extraction and transesterification hydrogenation, urea complex precipitation and argentation TLC have been applied prior to GC analysis of furan fatty acids.By using multidimensional GC-MSD with cooled injection and flow-controlled column switching with intermediate cold trapping, it has been possible to identify directly the methyl esters of furan fatty acids without further pre-analytical separation.The most common of the furan fatty acids can be subdivided into two groups depending on whether they bear a propyl or pentyl side group in the 5-position of the furan ring. In addition to the eight furan fatty acids known to be present in fish oil, six new ones were identified, four with propyl substitution and two with pentyl substitution. Four have earlier been reported to be present in the hepatopancreas of crayfish and in fish tissue, whereas the propyl-substituted 16,19-epoxy-17,18-dimethyldocosa-16,18-dienoic acid and the pentyl-substituted furan fatty acid 6,9-epoxy-7-methyltetradeca-6,8-dienoic acid were hitherto unknown.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 1597-1603 
    ISSN: 1434-1948
    Keywords: Phosphaalkynes ; Cooligomerization ; Phosphaalkyne cyclooligomers ; Cage compounds, phosphorus-carbon-aluminum ; Cage compounds, phosphorus-carbon-gallium ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: When trialkylaluminum reagents 2 bearing sterically demanding substituents are allowed to react with phosphaalkynes 1 a highly selective phosphaalkyne cyclotrimerization with incorporation of one organometal unit occurs (→ 5a-d). The resulting triphosphaalatricycloheptenes 5 are able to function as ligands in transition metal complexes (→ 6a,b), as illustrated by the reactions of 5a with nonacarbonyldiiron or the pentacarbonyltungsten tetrahydrofuran complex. When triethylgallium (7) is allowed to react with phosphaalkynes 1, tricyclic phosphorus-carbon-gallium compounds are generated (→ 8a,b).
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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