Goossen Lukas J, Goossen Käthe, Stanciu Corneliu
FB Chemie-Organische Chemie, TU Kaiserslautern, Erwin-Schrödinger-Strasse Geb. 54, 67663 Kaiserslautern, Germany.
Angew Chem Int Ed Engl. 2009;48(20):3569-71. doi: 10.1002/anie.200900329.
Crucial breakthroughs in the activation of the C(aryl)-O bond of phenol derivatives were achieved almost simultaneously by two research groups (see scheme; Cy = cyclohexyl). Garg et al. coupled a range of aryl pivalates with arylboronic acids to give unsymmetrical biaryls. Shi et al. achieved this through C(aryl)-O activation of aryl carboxylates; the best results for the coupling of aryl boroxines were again obtained with aryl pivalates.
两个研究小组几乎同时在酚类衍生物的C(芳基)-O键活化方面取得了关键突破(见示意图;Cy = 环己基)。加尔格等人将一系列芳基新戊酸酯与芳基硼酸偶联,得到不对称联芳基化合物。施等人则通过芳基羧酸盐的C(芳基)-O活化实现了这一目标;芳基硼酸酯偶联的最佳结果同样是使用芳基新戊酸酯获得的。