跳转至内容
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
摘要

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
货号
品牌
产品描述

Sigma-Aldrich
乙酰丙酸甲酯, ≥98.0%