Total Synthesis of (±)-Codonopiloneolignanin A

Org Lett. 2021 Aug 6;23(15):5684-5688. doi: 10.1021/acs.orglett.1c01803. Epub 2021 Jul 12.

Abstract

An intramolecular formal [3 + 2] cationic cycloaddition between benzylic carbocation and styrene was developed for the total synthesis of codonopiloneolignanin A. Further study shows benzocycloheptene as a good substrate for 1,3-dipolar cycloaddition, and a model study toward cephalocyclidine A skeleton was reported.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Cycloaddition Reaction
  • Lignans / chemical synthesis*
  • Lignans / chemistry
  • Molecular Structure
  • Stereoisomerism

Substances

  • Lignans