A General Synthetic Approach to Hydroquinone Meroterpenoids: Stereoselective Synthesis of (+)-(S)-Metachromin V and Alliodorol

@article{Serra2014AGS,
  title={A General Synthetic Approach to Hydroquinone Meroterpenoids: Stereoselective Synthesis of (+)-(S)-Metachromin V and Alliodorol},
  author={S. Serra and A. Cominetti and Veronica Lissoni},
  journal={Natural Product Communications},
  year={2014},
  volume={9}
}
  • S. Serra, A. Cominetti, Veronica Lissoni
  • Published 2014
  • Chemistry, Medicine
  • Natural Product Communications
    • A new general synthetic approach to hydroquinone meroterpenoids is here described. The framework of the aforementioned natural compounds was built up through the Li2CuCl4 catalysed cross coupling reaction of the 4-substituted-(E)-prenyl acetates 9 with 2,5-bis(benzyloxy)phenyl magnesium bromide 8 as a key step. The latter sp3-sp2 coupling affords the products in good chemical yields and in very high stereoisomeric purity. A further key step of the present synthetic method consists of the… CONTINUE READING
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