作者:Mathieu Dubernet、Virginie Caubert、Jérôme Guillard、Marie-Claude Viaud-Massuard
DOI:10.1016/j.tet.2005.03.016
日期:2005.5
Substituted bis(fur-2-yl), bis(fur-3-yl) and bis(thien-2-yl) maleimides with potential antidiabetic properties are described. Their synthesis involves, as a key step, a Suzuki cross-coupling between various boron derivatives and the diiodomaleimides. Therefore, a wide range of substituted symmetric and non-symmetric maleimide derivatives can be prepared.
描述了具有潜在抗糖尿病特性的取代的双(呋喃-2-基),双(呋喃-3-基)和双(噻吩-2-基)马来酰亚胺。作为关键步骤,它们的合成涉及各种硼衍生物与二碘亚胺之间的铃木交叉偶联。因此,可以制备各种取代的对称和非对称马来酰亚胺衍生物。