Synthesis of deoxynivalenol-glucosides and their characterization using a QTrap LC-MS/MS |
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Authors: | F. Berthiller R. Schuhmacher G. Buttinger M. Freudenschuss G. Adam R. Krska |
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Affiliation: | (1) Christian Doppler Laboratory for Mycotoxin Research, IFA-Tulln, Konrad Lorenz Str. 20, 3430 Tulln, Austria;(2) biopure Referenzsubstanzen GmbH, Konrad Lorenz Str. 20, 3430 Tulln, Austria;(3) Center of Applied Genetics, University of Agricultural Sciences, Muthgasse 18, 1190 Wien, Austria |
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Abstract: | Deoxynivalenol (DON)-glucosides were successfully synthesized in a two-step reaction from 1-β-Bromo-1-deoxy-2,3,4,6-tetra-O-acetyl-α-D-gluco-pyranose and 3-Acetyl-DON or 15-Acetyl-DON. After purification of the reaction products, the mycotoxin conjugates were for the first time characterized by means of a triple quadrupole mass spectrometer in combination with a linear ion trap. Due to different fragmentation behaviour it was also possible to distinguish between the two glucosides. Presented at the 25th Mykotoxin Workshop in Giessen, Germany, May 19–21, 2003 |
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Keywords: | deoxynivalenol-glucosides tandem mass spectrometry |
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