M. Beller et al., FIRST PALLADIUM-CATALYZED HECK REACTIONS WITH EFFICIENT COLLOIDAL CATALYST SYSTEMS, Journal of organometallic chemistry, 520(1-2), 1996, pp. 257-259
For the first time it has been shown that palladium colloids are effec
tive and active catalysts for the olefination of aryl bromides (Heck r
eaction). Worthy of note are the high activities of the catalyst syste
m for activated aryl bromides under optimized reaction conditions, whi
ch are better than or comparable with ''classical'' palladium phosphin
e complexes, Addition of phosphines strongly retards the reaction rate
of the colloid catalyst, Nevertheless, this type of catalyst is not s
u:table for the activation of non-activated substrates, especially tec
hnically interesting aryl chlorides.