Canadian journal of chemistry

Étude cinétique de l'ouverture thermique de la liaison CC d'aziridines et d'époxydes dipôles-1, 3 potentiels: I. Méthode d'étude expérimentale

A Derdour, F Texier

Index: Derdour, Aicha; Texier, Fernand Canadian Journal of Chemistry, 1985 , vol. 63, p. 2245 - 2252

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Citation Number: 9

Abstract

The thermolysis of the 2-cyanoaziridines (1), 2-alkoxycarbonylaziridines (2), 2-arylaziridines (3), and 2, 2-dicyano-3-aryloxiranes (4) leads to a rupture of the carbon-carbon bond yielding an azomethine ylide and the ylide of a carbonyl. The reaction of these ylides of azomethine with methyl acetylene dicarboxylate (MADC) leads to the formation of a 3- pyroline, which is transformed, according to the substituants, to a 2-pyrroline or to pyrrole. ...