Unusual long-chain, diunsaturated alkenones and alkyl alkenoates exhibiting double bonds separated by three methylene units instead of the more usual five were characterized by electron ionization (EI) gas chromatography/mass spectrometry. In a first step, the positions of the double bonds of these compounds (isolated from Holocene Black Sea sediments) were confirmed after OsO4 treatment and silylation. Mass spectra of the resulting tetratrimethylsilyloxy derivatives allowed unambiguous determination of the positions of unsaturations. The EI mass spectra of the non-derivatized compounds were then compared with those of the alkenones and alkyl alkenoates having double bonds separated by five methylene units. Specific fragment ions resulting from gamma-H rearrangements were found to be prominent in EI mass spectra of these unusual 'Black Sea' diunsaturated alkenones and alkyl alkenoates. These fragment ions can be used to characterize these compounds in natural samples without the need for laborious derivatization treatments.
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J Chromatogr A
May 2021
Department of Earth, Environmental and Planetary Sciences, Brown University, 324 Brook Street, Providence, Rhode Island 02912, USA. Electronic address:
Silver(I)-mercaptopropyl (Ag-MP) functionalized silica gel has demonstrated its effectiveness in separating various unsaturated organic compounds including unsaturated fatty acid ethyl esters (FAEEs), triglycerols (TAGs) and long-chain alkyl ketones (alkenones). While Ag-MP stationary phase displays many advantages over the conventional silver ion-impregnated silica gel (e.g.
View Article and Find Full Text PDFBeilstein J Org Chem
February 2021
Bayer AG, Research & Development Crop Science, Industriepark Höchst, 65926 Frankfurt, Germany.
A novel reactivity of 1,1,1-trifluoroalkanones is reported, where the reaction with AlCl results in the formation of 1,1-dichloro-1-alkenones. The reaction scope was found to be broad, with various chain lengths and aryl substituents tolerated. For substrates containing an electron-rich aromatic ring, further reactions take place, resulting in bicyclic and/or rearrangement products.
View Article and Find Full Text PDFJ Agric Food Chem
March 2020
Lehrstuhl für Allgemeine Lebensmitteltechnologie, Technische Universität München, Maximus-von-Imhof-Forum 2, D-85354 Freising, Weihenstephan, Germany.
A homologous series (C6-C10) of 2-mercapto-4-alkanols was obtained by the addition of thioacetic acid to the respective alkenones and subsequent reduction with LiAlH. Gas chromatographic separation of the stereoisomers was achieved using chiral stationary phases. Their absolute configurations were assigned by the correlation of H NMR data and enzyme-catalyzed kinetic resolutions.
View Article and Find Full Text PDFSci Rep
February 2018
Faculty of Life and Environmental Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki, 305-8572, Japan.
The cosmopolitan marine haptophyte alga Emiliania huxleyi accumulates very long-chain (C-C) alkyl ketones with two to four trans-type carbon-carbon double bonds (alkenones). These compounds are used as biomarkers of haptophytes and as palaeothermometers for estimating sea-surface temperatures in biogeochemistry. However, the biosynthetic pathway of alkenones in algal cells remains enigmatic, although it is well known that the C tri-unsaturated alkenone (K) becomes dominant at low temperatures, either by desaturation of K or by a separate pathway involving the elongation of tri-unsaturated alkenone precursors.
View Article and Find Full Text PDFRapid Commun Mass Spectrom
June 2006
Laboratoire de Microbiologie de Géochimie et d'Ecologie Marines (LMGEM-UMR 6117), Centre d'Océanologie de Marseille, F-13288 Marseille, France.
Unusual long-chain, diunsaturated alkenones and alkyl alkenoates exhibiting double bonds separated by three methylene units instead of the more usual five were characterized by electron ionization (EI) gas chromatography/mass spectrometry. In a first step, the positions of the double bonds of these compounds (isolated from Holocene Black Sea sediments) were confirmed after OsO4 treatment and silylation. Mass spectra of the resulting tetratrimethylsilyloxy derivatives allowed unambiguous determination of the positions of unsaturations.
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