- First enantioselective total synthesis of (+)-(R)-Pinnatolide using an asymmetric domino allylation reaction.
First enantioselective total synthesis of (+)-(R)-Pinnatolide using an asymmetric domino allylation reaction.
Organic letters (2012-08-03)
Lutz F Tietze, Thomas Wolfram, Julian J Holstein, Birger Dittrich
PMID22853329
RESUMEN
An efficient total synthesis of (+)-(R)-Pinnatolide is described. As a key step an asymmetric multicomponent domino allylation reaction of methyl levulinate is used to form the quaternary stereogenic center in a highly selective way.
MATERIALES