Zinc(II) mediated imine-enamine tautomerization

Org Lett. 2012 Jun 1;14(11):2698-701. doi: 10.1021/ol300874c. Epub 2012 May 14.

Abstract

Reduction of imine-anthracenone compounds selectively produces secondary alcohols leaving the external imine group unreacted. Addition of the Zn(II) ion induces a metal-mediated imine-enamine tautomerization reaction that is selective for Zn(II), a new fluorescence detection method not previously observed for this important cation.

Publication types

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

MeSH terms

  • Anthracenes / chemistry*
  • Crystallography, X-Ray
  • Fluorescence
  • Imines / chemical synthesis*
  • Imines / chemistry
  • Isomerism
  • Magnetic Resonance Spectroscopy
  • Molecular Conformation
  • Molecular Structure
  • Zinc / chemistry*

Substances

  • Anthracenes
  • Imines
  • Zinc