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Highly substituted pyridines via tethered imine-enamine (TIE) methodology
Authors:Raw Steven A  Taylor Richard J K
Affiliation:Department of Chemistry, University of York, Heslington, York, UKYO10 5DD. sar113@york.ac.uk
Abstract:A tethered imine-enamine 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 MnO(2)-mediated tandem oxidation processes (TOPs).
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