作者:Constantinos G. Neochoritis、Tryfon Zarganes-Tzitzikas、Michaela Novotná、Tatiana Mitríková、Zefeng Wang、Katarzyna Kurpiewska、Justyna Kalinowska-Tłuścik、Alexander Dömling
DOI:10.1002/ejoc.201901187
日期:2019.9.22
Boronic acids are amongst the most useful synthetic intermediates, frequently used by modern drug design. However, their access and fast synthesis of libraries are often problematic. We present a methodology on the synthesis of drug-like scaffolds via IMCRs with unprotected phenylboronic acids. To demonstrate an application of our approach, we also performed one-pot Suzuki couplings on the primary
硼酸是最有用的合成中间体之一,经常用于现代药物设计。然而,它们的访问和库的快速合成通常是有问题的。我们提出了一种通过 IMCR 与未保护的苯基硼酸合成类药物支架的方法。为了演示我们方法的应用,我们还在主要 MCR 支架上进行了单锅 Suzuki 耦合。此外,我们对剑桥结构数据库进行了彻底的数据挖掘,揭示了有趣的几何特征。