Exerting control over the acyloin reaction

Chem Commun (Camb). 2011 May 28;47(20):5849-51. doi: 10.1039/c1cc11654a. Epub 2011 Apr 18.

Abstract

A synthetic method for conducting the acyloin reaction using electron transfer in solution is reported. By linking two esters via their oxygen atoms, it was possible to perform crossed acyloin reactions between two different ester functionalities and display a high degree of preference for an intramolecular coupling process.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Electron Transport
  • Esters
  • Fatty Alcohols / chemistry*
  • Lithium / chemistry
  • Stereoisomerism

Substances

  • Esters
  • Fatty Alcohols
  • acyloin
  • Lithium