Issue 0, 1981

Routes to 3-aryl-5-phenyl-2-thioacylmethylene-2H-1,3,4-thiadiazolenes

Abstract

Prospective routes to the above compounds include reaction of an N′-arylbenzothiohydrazide or of its N′-acetyl derivative with thioacetic acid, when the thioacyl and acyl derivatives are formed, as well as by reaction of the 2-acylmethylene-3-aryl-5-phenyl-2H-1,3,4-thiadiazolenes with phosphorus pentasulphide. The 1H n.m.r. and mass spectra of these compounds are discussed.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1981, 2952-2955

Routes to 3-aryl-5-phenyl-2-thioacylmethylene-2H-1,3,4-thiadiazolenes

H. Mastalerz and M. S. Gibson, J. Chem. Soc., Perkin Trans. 1, 1981, 2952 DOI: 10.1039/P19810002952

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