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Suzuki Miyaura sterically hindered substrates

In 2001, Fu s group [128] reported the application of Pd-triarylphosphane-ferrocene catalysts for the Suzuki-Miyaura reaction on aryl chloride substrates (Figure 1.40a). Activated aryl chlorides could be coupled at room temperature, while unactivated aryl chlorides, including sterically hindered and electron-rich substrates, at 70 °C. The triarylphosphane - which is air stable - was mixed with either Pd2(dba)j or Pd(OAc)2 with KjPO -HjO as base in toluene at room temperature, and very good yields were obtained. [Pg.61]


See other pages where Suzuki Miyaura sterically hindered substrates is mentioned: [Pg.260]    [Pg.371]    [Pg.389]    [Pg.7]    [Pg.5650]    [Pg.5649]    [Pg.69]    [Pg.76]    [Pg.77]    [Pg.84]    [Pg.124]    [Pg.265]    [Pg.377]   
See also in sourсe #XX -- [ Pg.147 ]




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