| Literature DB >> 23604668 |
F Berthiller1, R Schuhmacher, G Buttinger, M Freudenschuss, G Adam, R Krska.
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.Entities:
Year: 2003 PMID: 23604668 DOI: 10.1007/BF02940092
Source DB: PubMed Journal: Mycotoxin Res ISSN: 0178-7888 Impact factor: 3.833