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Cover Feature: Total Synthesis, Stereochemical Assignment, and Divergent Enantioselective Enzymatic Recognition of Larreatricin (Chem. Eur. J. 59/2018)
Author(s) -
Martin Harry J.,
Kampatsikas Ioannis,
Oost Rik,
Pretzler Matthias,
AlSayed Emir,
Roller Alexander,
Giester Gerald,
Rompel Annette,
Maulide Nuno
Publication year - 2018
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201805128
Subject(s) - enantioselective synthesis , enantiomer , total synthesis , stereochemistry , lignan , chemistry , metabolite , cover (algebra) , absolute configuration , feature (linguistics) , secondary metabolite , biochemistry , philosophy , catalysis , gene , linguistics , mechanical engineering , engineering
Mirror, mirror on the wall , who is the fairest one of all? Larreatricin is a naturally occurring lignan with a long history of use in traditional medicine. However, its absolute configuration remains unknown and its biological activity is poorly understood. An efficient total synthesis allowing for the unambiguous assignment of the configuration of its enantiomers is presented. Polyphenol oxidases show high and remarkably divergent enantioselective recognition of this secondary metabolite. More information can be found in the Communication by H. J. Martin, A. Rompel, N. Maulide et al. on page 15756.