Synthesis and Assignment of Absolute Configuration of (−)-Oleocanthal: A Potent, Naturally Occurring Non-steroidal Anti-inflammatory and Anti-oxidant Agent Derived from Extra Virgin Olive Oils
journal contributionposted on 27.10.2005 by Amos B. Smith, Qiang Han, Paul A. S. Breslin, Gary K. Beauchamp
Any type of content formally published in an academic journal, usually following a peer-review process.
Effective total syntheses and the assignment of absolute configurations of both the (+)- and (−)-enantiomers of oleocanthal 1 (a.k.a. deacetoxy ligstroside aglycon), the latter derived from extra virgin olive oils and known to be responsible for the back of the throat irritant properties of olive oils, have been achieved. The absolute and relative stereochemistry of the naturally occurring enantiomer (−)-1 proved to be 3S,4E. Both syntheses begin with d-(−)-ribose, proceed in 12 steps, and are achieved with an overall yield of 7%. Both enantiomers proved to be non-steroidal anti-inflammatory and anti-oxidant agents.