The Suzuki–Miyaura reaction is one of the most powerful tools for the formation of carbon–carbon bonds in organic synthesis. The utilization of alcohols in this powerful reaction is a challenging task. This short review covers progress in the transition-metal-catalyzed Suzuki­–Miyaura-type cross-coupling reaction of π-activated alcohol, such as aryl, benzylic, allylic, propargylic and allenic alcohols, between 2000 and June 2019.

中文翻译：

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过渡金属催化的π-活化醇的Suzuki-Miyaura型交叉偶联反应

铃木-宫浦反应是有机合成中碳-碳键形成最强大的工具之一。在这种强大的反应中利用醇是一项艰巨的任务。这篇简短的综述涵盖了2000年至2019年6月之间过渡金属催化的s-活化醇（例如芳基，苄基，烯丙基，丙炔基和烯丙醇）的Suzuki-Miyaura型交叉偶联反应的进展。