Zinc(II) Mediated Imine–Enamine Tautomerization
Organic Letters2012Vol. 14(11), pp. 2698–2701
Citations Over Time
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.
Related Papers
- → Deuteration of Aromatic Rings under Very Mild Conditions through Keto-Enamine Tautomeric Amplification(2015)20 cited
- → Zinc(II) Mediated Imine–Enamine Tautomerization(2012)27 cited
- → Equilibria between enamine and α,β-unsaturated imine in cephalosporin hydrolysis(1986)7 cited
- → Imine-enamine tautomerization of dihydroazolopyrimidines 4. Synthesis and tautomerization of 5-(2-hydroxyphenyl)-dihydro-1,2,4-triazolo[1,5-a]pyrimidines(1993)4 cited
- → The oxidation of compounds capable of imine-enamine tautomerism with lead tetraacetate(1975)7 cited