This paper describes the study of the arylation of isoprene, (E)-penta-1,3-diene and 2,3-dimethylbuta-1,3-diene with palladium complexes. In every case, the regioselectivity of the reaction is established on 1H-NMR data. Mechanisms are proposed in order to explain the results obtained for the five reactions.
K. Saïd, Y. Moussaoui, R. Ben Salem
arylation, diènes conjugués, complexes palladiés, mécanismes réactionnels