75737-56-3Relevant academic research and scientific papers
Structural determination of ε-lactams by 1H and 13CNMR
Ruben, Montalvo-Gonzaleza,Armando, Ariza-Castolob
experimental part, p. 1013 - 1018 (2010/08/05)
The thermodynamic products (ε-lactams) of the degradation of ten different spirocyclic oxaziridines were analyzed by 1H and 13C NMR spectroscopy. The preferred conformations were determined by examining the homonuclear spin-spin coup
Photolyse d'oxaziridines. 10. Photolyse et thermolyse d'oxaziridines N-arylees
Oliveros, Esther,Riviere, Monique,Lattes, Armand
, p. 1025 - 1027 (2007/10/02)
The nature of the nitrogen substituent does not affect the regioselectivity of lactams derived from photolysis or thermolysis of spirooxaziridines.The thermolysis of N-arylspirooxaziridines is a very good synthetic method to obtain N-aryl heterocycles.
