Oxidative debenzylation of N-benzyl amides and O-benzyl ethers using alkali metal bromide

Org Lett. 2014 Jul 18;16(14):3812-5. doi: 10.1021/ol501703y. Epub 2014 Jun 30.

Abstract

The oxidative debenzylation of N-benzyl amides and O-benzyl ethers was promoted with high efficiency by a bromo radical formed through the oxidation of bromide from alkali metal bromide under mild conditions. This reaction provided the corresponding amides from N-benzyl amides and carbonyl compounds from O-benzyl ethers in high yields.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amides / chemistry*
  • Benzyl Compounds / chemistry*
  • Bromides / chemistry*
  • Ethers / chemistry*
  • Metals, Alkali / chemistry*
  • Molecular Structure
  • Oxidation-Reduction

Substances

  • Amides
  • Benzyl Compounds
  • Bromides
  • Ethers
  • Metals, Alkali