Document Type: Research Article
Department of Chemistry, Isfahan University of Technology, P.O. Box 84156 Isfahan, I.R. IRAN
Conformational properties of N-aryl-1-azacyclooctan-5- ones with a p-methyl, m-methyl, and p-methoxy group as a substituent have been studied by 1H-NMR, 13C-NMR and IR spectroscopies. Transannular interaction of the two functional groups have been examined from the ring inversion barriers and the carbonyl vibrational frequencies with reference to the corresponding data of the respective monofunctional and difunctional compounds.