The structure of vinyl amine and its reactivity towards a proton is studied by the PRDDO SCF MO method. The equilibrium structure is found to be non‐planar and barriers to inversion‐ and rotation‐dominated processes are calculated. Proton addition to vinyl amine, as a model of enamine protonation, is examined by means of electrostatic molecular potentials and C ‐ versus N ‐proton affinities.
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Müller et al. (1978) studied this question.
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