Highly efficient oxidation of amines to imines by singlet oxygen and its application in Ugi-type reactions

Org Lett. 2009 Oct 15;11(20):4568-71. doi: 10.1021/ol9018166.

Abstract

A variety of secondary benzylic amines were oxidized to imines in 90% to >99% yields by singlet oxygen generated from oxygen and a porphyrin photosensitizer. On the basis of these reactions, a protocol was developed for oxidative Ugi-type reactions with singlet oxygen as the oxidant. This protocol has been used to synthesize C1- and N-functionalized benzylic amines in up to 96% yields.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amines / chemistry*
  • Imines / chemistry*
  • Oxidation-Reduction
  • Singlet Oxygen / chemistry*

Substances

  • Amines
  • Imines
  • Singlet Oxygen