Issue 0, 1980

The photocyclisation of 1,2-Ciarylpyridinium cations and the photobiscyclisation of 1,2,6-triarylpyridinium cations

Abstract

Photocyclisation of 1-(2-pyridyl)-2-arylpyridiniums yields benzo[c]pyrido[1,2-a]-1,8-naphthyridinylinium cations. Photobiscyclisation of 1,2,6-triarylpyridiniums gives benzo[8,9]quinolizino[4,5,6,7-fed]phenanthridinylium cations and their 9-aza-derivatives. Electron donor substituents tend to lower the yields which are otherwise high. The structures are supported by X-ray crystallographic analysis and by ultraviolet and n.m.r. spectra.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1980, 1879-1887

The photocyclisation of 1,2-Ciarylpyridinium cations and the photobiscyclisation of 1,2,6-triarylpyridinium cations

A. R. Katritzky, Z. Zakaria and E. Lunt, J. Chem. Soc., Perkin Trans. 1, 1980, 1879 DOI: 10.1039/P19800001879

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