Electrophotocatalytic Acetoxyhydroxylation of Aryl Olefins

J Am Chem Soc. 2021 May 19;143(19):7247-7252. doi: 10.1021/jacs.1c01967. Epub 2021 May 5.

Abstract

A method for the acetoxyhydroxylation of olefins with syn stereoselectivity under electrophotocatalytic conditions is described. The procedure uses a trisaminocyclopropenium (TAC) ion catalyst with visible light irradiation under a controlled electrochemical potential to convert aryl olefins to the corresponding glycol monoesters with high chemo- and diastereoselectivity. This reaction can be performed in batch or in flow, enabling multigram synthesis of the monoester products.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Alkenes / chemistry*
  • Catalysis
  • Cyclopropanes / chemistry*
  • Esters / chemical synthesis*
  • Esters / chemistry
  • Hydroxylation
  • Molecular Structure
  • Stereoisomerism

Substances

  • Alkenes
  • Cyclopropanes
  • Esters