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SuFEx-Enabled Direct Deoxy-Diversification of Alcohols.

Amaechi Shedrack OdohCourtney KeelerByoungmoo Kim
Published in: Organic letters (2024)
We introduce a new use of sulfonyl fluoride as a bifunctional reagent that facilitates the one-step deoxy-diversification of complex alcohol libraries. Our reaction design features a Sulfur(VI) Fluoride Exchange (SuFEx) mediated activation of alcohols and fluoride-induced activation of silicon-bound nucleophiles. This method enables the direct conversion of alcoholic C-O bonds in complex molecules into diverse analogues via C-C, C-N, C-Cl, and C-Br bond formation while suppressing any elimination side-products.
Keyphrases
  • drinking water
  • high glucose
  • drug induced
  • liver injury
  • diabetic rats
  • signaling pathway
  • molecular docking
  • endothelial cells
  • oxidative stress
  • alcohol consumption
  • highly efficient
  • metal organic framework