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First enantioselective total synthesis of (+)-(R)-Pinnatolide using an asymmetric domino allylation reaction
Authors:Tietze Lutz F  Wolfram Thomas  Holstein Julian J  Dittrich Birger
Affiliation:Institute of Organic and Biomolecular Chemistry, Georg-August-University of G?ttingen, Tammannstr. 2, D-37077 G?ttingen, Germany. ltietze@gwdg.de
Abstract: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.
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