Issue 16, 1984

Novel desulphurization of thiourea derivatives by alkaline autoxidation

Abstract

Autoxidation of 1,3-disubstituted thioureas in the presence of oxygen and tertiary butoxide in tertiary butanol afforded the corresponding ureas in good yields together with small amounts of the corresponding guanidines while the same treatment of benz- or naphth-imidazole-2-thiones gave the parent imidazoles and the 2-sulphonic acids.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1984, 1064-1065

Novel desulphurization of thiourea derivatives by alkaline autoxidation

Y. H. Kim, H. J. Kim and G. H. Yon, J. Chem. Soc., Chem. Commun., 1984, 1064 DOI: 10.1039/C39840001064

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