Issue 0, 1979

Iminyls. Part 3. Formation of triaryl-pyridines and -pyrimidines from aryl-β-arylvinyliminyls

Abstract

Aryl-β-arylvinyliminyls, produced by oxidation of the corresponding imino-oxyacetic acids with persulphate or by thermolysis of the t-butyl peresters of these acids, abstract hydrogen giving imines which dimerise and/or are hydrolysed to ketones. The bicyclic dimers so formed readily undergo oxidative fragmentation to triaryl-pyridines and/or -pyrimidines.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1979, 616-620

Iminyls. Part 3. Formation of triaryl-pyridines and -pyrimidines from aryl-β-arylvinyliminyls

A. R. Forrester, M. Gill and R. H. Thomson, J. Chem. Soc., Perkin Trans. 1, 1979, 616 DOI: 10.1039/P19790000616

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