Issue 14, 1981

Anomalous products from 1,2,5-triaza- and 1,5-diaza-pentadiene thermolyses: formation of amidines and pyrroles, respectively

Abstract

Gas-phase thermolysis of the dimethylamino-azoalkene (1) gives the formamidine (2) by loss of HCN: in contrast, the related 1,5-diazapentadiene (4) under more forcing conditions gives aniline (30%) and N-methyl-pyrrole (43%).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1981, 722-723

Anomalous products from 1,2,5-triaza- and 1,5-diaza-pentadiene thermolyses: formation of amidines and pyrroles, respectively

H. McNab and E. Murray, J. Chem. Soc., Chem. Commun., 1981, 722 DOI: 10.1039/C39810000722

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