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Although anti-β-hydride elimination is postulated in the arylation of arenes, examples are relatively scarce. For an example, see:, C. C. Hughes, D. Trauner, Angew. Chem. 2002, 114, 2331
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Since the rotational barrier of an amide bond is usually high, the π-coordination between acryl olefin and the palladium center in 3 a would likely help to maintain the staggered conformation (see Scheme 8), which inhibits β-hydride elimination. For a recent study on amide C-N bond rotation, see:, C. R. Kemnitz, M. J. Loewen, J. Am. Chem. Soc. 2007, 129, 2521.
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