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Concerted addition background

Overall, these early studies of carboxylate-assisted intramolecular C-H activation established the key features of these AML A/CMD processes, where an electron-deficient metal center works in concert with a pendant carboxylate base to promote C-H activation. This is most evident when an agostic intermediate is involved and such species also rationalize how these systems can also perform C(sp )-H bond activation. Whether C-H activation is achieved as a one- or two-step process appears rather system dependent. Alternative mechanisms, for example, proton transfer onto a halide ligand, oxidative addition, or AMLA-4 processes involving proton transfer onto the inner (Pd-bound) oxygen of the carboxylate were all ruled out. Likewise, no evidence for S Ar processes had been reported. Subsequent work was set against this background and considered the various other parameters that may affect the C-H bond activation process. [Pg.5]


See other pages where Concerted addition background is mentioned: [Pg.173]    [Pg.467]    [Pg.356]    [Pg.356]    [Pg.155]    [Pg.247]    [Pg.519]    [Pg.336]    [Pg.356]    [Pg.158]    [Pg.33]    [Pg.1341]    [Pg.1341]   
See also in sourсe #XX -- [ Pg.376 ]




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