作者:Toufike Kanouni、Qing Dong、Benjamin Abelovski、Michael B. Wallace
DOI:10.1016/j.tetlet.2010.11.063
日期:2011.1
A novel, efficient route for the synthesis of 1,8-naphthyridine-2,5-dione compounds is reported. The synthetic scheme allows for diversification at the 4-position of the core, and it was utilized to develop a series of inhibitors for MEK kinase.
报道了一种新颖的合成1,8-萘啶-2,5-二酮化合物的有效途径。合成方案允许在核心的4位进行多样化,并被用于开发一系列MEK激酶抑制剂。