Issue 0, 1974

Reactions of NN-dialkylanilines with diethyl azodicarboxylate and with ozone

Abstract

Thermolysis of the adduct formed from N-phenylpyrrolidine and diethyl azodicarboxylate leads to a mixture of isomeric dimers whose structures and mechanisms of formation have been elucidated. The same dimers are formed by ozonation of N-phenylpyrrolidine. Other NN-dialkylanilines and their reactions with the azodicarboxylate as well as with ozone are described.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1974, 1614-1619

Reactions of NN-dialkylanilines with diethyl azodicarboxylate and with ozone

G. H. Kerr, O. Meth-Cohn, E. B. Mullock and H. Suschitzky, J. Chem. Soc., Perkin Trans. 1, 1974, 1614 DOI: 10.1039/P19740001614

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