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Merck
  • 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
要旨

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.

材料
製品番号
ブランド
製品内容

Sigma-Aldrich
レブリン酸メチル, ≥98.0%