Design, Synthesis, and Implementation of Sodium Silylsilanolates as Silyl Transfer Reagents
作者:Hiroki Yamagishi、Hayate Saito、Jun Shimokawa、Hideki Yorimitsu
DOI:10.1021/acscatal.1c02733
日期:2021.8.20
There is an increasing demand for facile delivery of silyl groups onto organic bioactive molecules. One of the common methods of silylation via a transition-metal-catalyzed coupling reaction employs hydrosilane, disilane, and silylborane as major silicon sources. However, the labile nature of the reagents or harsh reaction conditions sometimes render them inadequate for the purpose. Thus, a more versatile
对将甲硅烷基轻松传递到有机生物活性分子上的需求不断增加。通过过渡金属催化偶联反应进行硅烷化的一种常用方法是使用氢硅烷、乙硅烷和甲硅烷基硼烷作为主要的硅源。然而,试剂的不稳定性质或苛刻的反应条件有时使其不适合该目的。因此,需要更通用的甲硅烷基替代来源。我们在此报告了可储存的甲硅烷基硅烷醇钠的设计、合成和实施,该钠可用于在钯催化剂存在下芳基卤化物和拟卤化物的甲硅烷基化。所开发的方法允许对具有各种甲硅烷基的多官能化合物进行后期官能化。