Abstract
Bis(imidazolium) chlorides based on 1,2-phenylenediamine were introduced as efficient ligand precursors in the Pd-catalyzed Mizoroki-Heck cross-coupling reactions of substituted aryl halides with activated alkenes to afford the corresponding functionalized alkenes. While high to excellent yields (78–96%) were obtained with aryl bromides, moderate yields (51–59%) were achieved for aryl chlorides in this protocol.
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