INVERTOMERS AT NITROGEN IN AZIRIDINE СARBOXYLATES BY MULTINUCLEAR (<sup>1</sup>H, <sup>13</sup>С, <sup>17</sup>O AND <sup>15</sup>N) NMR STUDY
Abstract
A configurational and conformational study of N-unsubstituted, N-acetyl- and N-sulfonylaziridiine carboxylates has been performed by 1Н, 13С , 17O and 15N NMR spectroscopy. The presence of acetyl and sulfonyl groups on the ring nitrogen atom seems to reduce greatly the configurational stability at nitrogen.
How to Cite
Forni, A.; Moretti, I.; Mucci, A.; Prati, F.; Schenetti, L. Chem. Heterocycl. Compd. 1995, 31, 1071. [Khim. Geterotsikl. Soedin. 1995, 1226.]
For this article in the English edition, see DOI https://doi.org/10.1007/BF01165053
