Issue 0, 1967

NN-di-(1-cyanoalkyl)hydroxylamines. Part IV. Isolation of acyclic nitrones and their reaction with hydrogen cyanide

Abstract

α-Hydroxyamino-nitriles react with aldehydes to give the corresponding crystalline N-alkylidene-N-(1-cyanoalkyl)N-oxides. These acyclic nitrones are monomeric and fairly stable. The reaction of the nitrones with hydrogen cyanide gives NN-di-(1-cyanoalkyl)hydroxylamines almost quantitatively.

Article information

Article type
Paper

J. Chem. Soc. C, 1967, 2022-2023

NN-di-(1-cyanoalkyl)hydroxylamines. Part IV. Isolation of acyclic nitrones and their reaction with hydrogen cyanide

M. Masui and C. Yijima, J. Chem. Soc. C, 1967, 2022 DOI: 10.1039/J39670002022

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