Catalytic hydrotrifluoromethylation of unactivated alkenes

J Am Chem Soc. 2013 Feb 20;135(7):2505-8. doi: 10.1021/ja401022x. Epub 2013 Feb 7.

Abstract

A visible-light-mediated hydrotrifluoromethylation of unactivated alkenes that uses the Umemoto reagent as the CF(3) source and MeOH as the reductant is disclosed. This effective transformation operates at room temperature in the presence of 5 mol % Ru(bpy)(3)Cl(2); the process is characterized by its operational simplicity and functional group tolerance.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Alkenes / chemistry*
  • Catalysis
  • Fluorine / chemistry*
  • Methylation
  • Molecular Structure

Substances

  • Alkenes
  • Fluorine