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Reactions of benzoyl isothiocyanate with some carbodiimides and sulfinylamines

O. Hritzová and A. Trelová

Department of Organic Chemistry and Biochemistry, Faculty of Natural Sciences, P. J. Šafárik University, 041 67 Košice

 

Abstract:  Benzoyl isothiocyanate enters the reaction with N-cyclohexyl-N'-phenylcarbodiimide under the formation of benzoylanilide and the appropriate (4 + 2) cycloadduct on the phenyl—N = С bond of carbodiimide. On the other hand, the reactions of benzoyl isothiocyanate with N-methyl-N'-phenylcarbodiimide, N-sulfinylaniline, and N-sulfinylcyclohexylamine, respectively, result in differently substituted ureas and thioureas as well as in one unknown compound.

Full paper in Portable Document Format: 355a685.pdf

 

Chemical Papers 35 (5) 685–689 (1981)

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