Highly substituted pyridinesvia tethered imine–enamine (TIE) methodology
Steven A. Raw,Richard J. K. Taylor
Chemical Communications Pub Date : 01/27/2004 00:00:00 , DOI:10.1039/B316107B
Abstract

A tethered imineenamine methodology has been developed for the direct conversion of 1,2,4-triazines into highly substituted pyridines via the inverse electron demand Diels–Alder reaction which avoids the need for a discrete aromatisation step. This TIE methodology has also been applied in one pot reaction cascades involving 1,2,4-triazines and utilising MnO2-mediated tandem oxidation processes (TOPs).

Graphical abstract: Highly substituted pyridines via tethered imine–enamine (TIE) methodology