Issue 0, 1979

Iminyls. Part 2. Intramolecular aromatic substitution by iminyls. A new route to phenanthridines and quinolines

Abstract

Biphenyl-2-yl- and triarylvinyl-iminyls, generated by oxidation of the corresponding imino-oxyacetic acids with persulphate and by thermolysis of the t-butyl peresters of these acids, readily cyclise in high yield to phenanthridines and quinolines, respectively.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1979, 612-615

Iminyls. Part 2. Intramolecular aromatic substitution by iminyls. A new route to phenanthridines and quinolines

A. R. Forrester, M. Gill, J. S. Sadd and R. H. Thomson, J. Chem. Soc., Perkin Trans. 1, 1979, 612 DOI: 10.1039/P19790000612

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