Abstract
A series of 3-substituted and 3,3-disubstituted O-ethylvalerolactims were synthesized by interaction of the appropriate derivatives of valerolactam with triethyloxonium fluoroborate. Based on data from potentiometric titration, UV spectra and on the deuteration of O-ethylvalerolactim with CD 3OD (NMR spectra) imine—enamine tautomerism has been discovered in unsubstituted and 3-substituted O-ethylvaleractims.
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