prepared β-aryl-α-isocyano-acrylates and the commercially available Togni reagent as the CF3 radical precursor is described. These transformations occur in the absence of any transition metals and the title compounds are obtained in moderate to excellent yields. This protocol comprises a trifluoromethylation with concomitant isoquinoline framework construction.
                                    描述了一种简单有效的方法,从易于制备的β-芳基-α-异
氰基丙烯酸酯和市售的Togni试剂作为CF 3自由基前体开始,对
生物学上重要的1-三
氟甲基化
异喹啉具有重要意义。这些转化在不存在任何过渡
金属的情况下发生,并且标题化合物以中等至优异的产率获得。该方案包括三
氟甲基化以及相应的
异喹啉骨架结构。