Diazaphospholene-Catalyzed Hydrodefluorination of Polyfluoroarenes with Phenylsilane via Concerted Nucleophilic Aromatic Substitution

J Org Chem. 2022 Jan 7;87(1):294-300. doi: 10.1021/acs.joc.1c02360. Epub 2021 Dec 21.

Abstract

The metal-free catalytic C-F bond activation of polyfluoroarenes was achieved with diazaphospholene as the catalyst and phenylsilane as the terminal reductant. Density functional theory calculations suggested a concerted nucleophilic aromatic substitution mechanism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Metals*

Substances

  • Metals