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Unsaturated electrophiles, cross-coupling, organometallic

First, coordinatively unsaturated active palladium catalyst, PdL2, is produced via dissociation of the ligands, which then reacts with acyl halide to give the acylpalladium intermediate. Since deinsertion of CO of the acylpalladium derivatives may occur simul-taneously, the next step, transmetallation (so-called metathesis), is the most crucial for the efficiency of the overall reaction. A variety of organometallic compounds, such as boron, aluminum, copper, zinc, mercury, silicon, tin, lead, zirconium, and bismuth, are used as the partner in this coupling reaction without loss of CO. In this section, the important features of the cross-coupling reactions of a variety of organometallic compounds with acyl halides and related electrophiles are discussed. [Pg.635]


See other pages where Unsaturated electrophiles, cross-coupling, organometallic is mentioned: [Pg.9]    [Pg.561]    [Pg.133]    [Pg.347]    [Pg.98]    [Pg.651]    [Pg.143]    [Pg.725]    [Pg.226]   


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Coupling, organometallic organometallics

Cross-coupling electrophiles

Cross-coupling organometallics

Electrophiles, organometallic

Electrophilic coupling

Organometallic couplings

Organometallic cross-coupling

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