Herein we describe an alternative and unconventional approach of an aminocarbonylation reaction to access aryl amides from readily available and low-cost arylboronic acids and nitroarenes. Nickel metal can serve as both reductant and catalyst in this direct aminocarbonylation. This protocol exhibits a good functional group compatibility and allows a variety of aryl amides to be synthesized, including
本文中,我们描述了一种
氨基羰基化反应的替代性和非常规方法,可从容易获得的低成本芳基
硼酸和硝基
芳烃中获得芳基
酰胺。在这种直接的
氨基羰基化反应中,
镍金属既可以充当还原剂,又可以充当
催化剂。该方案显示出良好的官能团相容性,并允许合成多种芳基
酰胺,包括几种药物样分子。