copper-catalyzed cross-coupling of glycosyl thiosulfonate and boronic acid for the construction of thioglycosides is described. The good functional group compatibility of this method allows the preparation of many bioactive aryl/alkenyl thioglycosides, including the hSGLT1 inhibitor.
描述了用于构建
硫代糖苷的糖基
硫代
磺酸盐和
硼酸的有效且立体保留的
铜催化交叉偶联。该方法良好的官能团相容性使得可以制备许多具有
生物活性的芳基/烯基
硫代糖苷,包括hSGLT1
抑制剂。