Natural Products and Bioprospecting (May 2024)

Hydroxymethylation hydroxylation of 1,3-diarylpropene through a catalytic diastereoselective Prins reaction: cyclization logic and access to brazilin core

  • Xin-Ting Hu,
  • Qing-Yan Cheng,
  • Yan-Ping Chen,
  • Kun Li,
  • Cai-Xian Yan,
  • Dashan Li,
  • Li-Dong Shao

DOI
https://doi.org/10.1007/s13659-024-00450-2
Journal volume & issue
Vol. 14, no. 1
pp. 1 – 16

Abstract

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Abstract A catalytic diastereoselective Prins reaction for hydroxymethylation and hydroxylation of 1,3-diarylpropene was successfully utilized to prepare various 1,3-dioxanes 7 in 14–88% yields. Take advantage of the synthetic intermediate 7h, the key B/C rings in brazilin core could be constructed by the sequential of Friedel–Crafts/Ullmann-Ma rather than Ullmann-Ma/Friedel–Crafts reactions. Graphical Abstract

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