Enantioselective enolate protonation with chiral anilines: Scope, structural requirements, and mechanistic implications

High enantioselectivity has been demonstrated in the protonation of N,N-dii sopropyl amides (Table 1, entries 1-4, 7, and 10-13) derived from certain b eta,gamma unsaturated acids. Depending on double bond geometry and the degr ee of substitution at the gamma-carbon, gamma-protonation can be a competin g reaction in the case of the aliphatic substrates 12, 14b, 14d, and 18. Th e evidence is most consistent with a mechanism that involves proton transfe r from la to a mixed aggregate consisting of enolate 4a and the lithiated a mide 5, but direct proton transfer from la to the enolate is not ruled out.