Palladium‐Catalyzed Reductive [5+1] Cycloaddition of 3‐Acetoxy‐1,4‐enynes with CO: Access to Phenols Enabled by Hydrosilanes
作者:Li‐Jun Wu、Ren‐Jie Song、Shenglian Luo、Jin‐Heng Li
DOI:10.1002/anie.201808388
日期:2018.10
cycloaddition of 3‐acetoxy‐1,4‐enynes with CO, enabled by hydrosilanes, has been developed for delivering valuable functionalized phenols. This methodology employs hydrosilanes as the external reagent to facilitate the [5+1] carbonylative benzannulation. The reaction is a conceptually and mechanistically novel carbonylative cycloaddition route for the construction of substituted phenols, through the
已经开发了一种新的钯催化的3-乙酰氧基-1,4-炔烃与CO的钯催化还原[5 + 1]环加成反应,该反应由氢化硅烷实现,可提供有价值的官能化酚。该方法采用氢硅烷作为外部试剂,以促进[5 + 1]羰基苯环化反应。该反应在概念上和机理上都是新颖的羰基化环加成路线,可通过形成四个新的化学键形成具有卓越的官能团耐受性的取代酚。