Issue 22, 1979

Reactions of nitroalkenes with ynamines; synthesis of stable four-membered cyclic nitrones and X-ray crystal structure of 2-(NN-diethylcarbamoyl)-2,4-dimethyl-3-phenyl-2,3-dihydroazete 1-oxide

Abstract

2,3-Dihydroazete 1-oxides (3be), the first examples of crystalline, ‘stable’, four-membered cyclic nitrones, are formed by reaction of 1-nitroalkenes with ynamines, and other products are 3-nitrocyclobutenes; the structure of the cyclic nitrone (3b) has been determined by X-ray crystallography.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1979, 993-995

Reactions of nitroalkenes with ynamines; synthesis of stable four-membered cyclic nitrones and X-ray crystal structure of 2-(NN-diethylcarbamoyl)-2,4-dimethyl-3-phenyl-2,3-dihydroazete 1-oxide

A. D. de Wit, M. L. M. Pennings, W. P. Trompenaars, D. N. Reinhoudt, S. Harkema and O. Nevestveit, J. Chem. Soc., Chem. Commun., 1979, 993 DOI: 10.1039/C39790000993

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