Christian Doppler Laboratory for Mycotoxin Research, IFA-Tulln, Konrad Lorenz Str. 20, 3430, Tulln, Austria.
Mycotoxin Res. 2003 Mar;19(1):47-50. doi: 10.1007/BF02940092.
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.
脱氧雪腐镰刀菌烯醇(DON)-葡萄糖苷通过两步反应,从 1-β-溴-1-脱氧-2,3,4,6-四-O-乙酰基-α-D-吡喃葡萄糖和 3-乙酰基-DON 或 15-乙酰基-DON 成功合成。在反应产物纯化后,首次采用三重四极杆质谱仪与线性离子阱联用的方法对真菌毒素缀合物进行了表征。由于不同的裂解行为,也可以区分两种葡萄糖苷。