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Cinnamyl halides, reduction

This reaction profile, also called carbonylation, governs the reactivity of Pd-carbonyl complexes. Anionic M[Pd(CO)l3], for instance, catalyzes the reductive carbonylation of esters.f On the other hand, Pd(CO)(PPh3)3 was reported to catalyze the carboxymethy-lation of organic halides and the cyclocarbonylation of cinnamyl halides.f " However, the Pd-CO complexes are most often generated in situ from preformed alkyl -palladium complexes and CO under stoichiometric or catalytic conditions, for example, in the copolymerization of alkenes and CO. Decarbonylation reactions also involve the intermediacy of Pd-CO complexes. In this case, migratory deinsertion (Sect, n.3.1), that is, the microscopic reversal of the migratory insertion, takes place. [Pg.149]


See other pages where Cinnamyl halides, reduction is mentioned: [Pg.676]    [Pg.173]    [Pg.168]    [Pg.50]    [Pg.23]    [Pg.293]    [Pg.98]   
See also in sourсe #XX -- [ Pg.676 ]




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