Intramolecular Pd-Mediated Processes of Amino-Tethered Aryl Halides and Ketones: Insight into the Ketone α-Arylation and Carbonyl-Addition Dichotomy. A New Class of Four-Membered Azapalladacycles

An exploration of the scope and limitations of Pd(0)-catalyzed intramolecular coupling reactions
of amino-tethered aryl halides and ketones has been conducted. Two different and competitive reaction
pathways starting from ω-(2-haloanilino) alkanones, enolate arylation and addition to the carbonyl group,
have been observed, while ω-(2-halobenzylamino) alkanones exclusively underwent the enolate arylation
process. The dichotomy between ketone α-arylation and carbonyl-addition in the reactions of ω-(2-haloanilino) alkanones has been rationalized by the intermediacy of unprecedented four-membered
azapalladacycles, from which X-ray data and chemical behavior are reported.