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Front Cover: Synthesis of Isotope‐Labeled Deoxynivalenol‐15‐ O ‐Glycosides (Eur. J. Org. Chem. 47/2017)
Author(s) -
Weber Julia,
Fruhmann Philipp,
Hametner Christian,
Schiessl Alois,
Häubl Georg,
Fröhlich Johannes,
Mikula Hannes
Publication year - 2017
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Reports
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.201701632
Subject(s) - front cover , chemistry , mycotoxin , glycosylation , conjugated system , glycosyl , lewis acids and bases , glycoside , conjugate , stereochemistry , organic chemistry , cover (algebra) , catalysis , biochemistry , mechanical engineering , engineering , mathematical analysis , food science , mathematics , polymer
The Front Cover shows the synthesis of an isotope‐labeled glucoside of the mycotoxin deoxynivalenol. Lewis acid catalyzed glycosylation of acetyl‐protected deoxynivalenol was achieved using [ 13 C 6 ]glycosyl imidates as donors followed by deprotection to obtain conjugated mycotoxins in an optimized one‐pot procedure as isotope‐labeled reference compounds for ongoing studies in the field of masked and conjugated mycotoxins. We acknowledge Natallia Yelavik for the design of the cover. More information can be found in the Full Paper by H. Mikula et al.