A sequence of double Mizoroki-Heck reaction of vinylboronate pinacol ester with aryl halides followed by Suzuki-Miyaura coupling of thus-generated β,β-diarylvinylboronate esters with alkyl halides produces pharmaceutically important 1,1-diaryl-1-alkenes very efficiently. In the Pd-catalyzed Suzuki-Miyaura coupling step, the use of bulky electron-rich ligands such as P(t-Bu)2Me and PCy2(t-Bu) were found to be very effective.
乙烯硼酸频哪醇酯与芳基卤化物发生一系列双 Mizoroki-Heck 反应,然后由此产生的 β,β-二芳基
乙烯硼酸酯与烷基卤化物发生 Suzuki-Miyaura 偶联反应,可非常有效地生成具有重要药用价值的 1,1-二芳基-1-烯烃。在由
钯催化的 Suzuki-Miyaura 偶联反应步骤中,使用体积较大的富电子
配体(如 P(t-Bu)2Me 和 PCy2(t-Bu))非常有效。