246. The reactivity of organophosphorus compounds. Part XII. Nitrosation of phosphoramidates

PJ Bunyan, JIG Cadogan

Index: Bunyan,P.J.; Cadogan,J.I.G. Journal of the Chemical Society, 1962 , p. 1304 - 1308

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Citation Number: 7

Abstract

Nitrosation of N-arylphosphoramidates by nitrosylsulphuric acid* or nitrosyl chloride leads to the corresponding diazonium phosphate, probably produced by rapid rearrangement of the first formed N-nitrosophosphoramidates which were too reactive to be isolated. The resulting