substrates from feedstock materials, has been developed. The versatility of this approach arises, on the one hand, from the variety of cyclopentenes affordable through the key gold-catalyzed cycloisomerization step and, on the other hand, from its modular nature that allows the introduction of an à la carte substituent at position 2 employing a Suzuki coupling.
已经开发出一种从 1-
溴炔(原料中容易获得的底物)构建
吡啶的 4 步序列。这种方法的多功能性一方面源于通过关键的
金催化环异构化步骤可承受的各种
环戊烯,另一方面源于其模块化性质,允许在位置 2 引入点菜取代基采用铃木联轴器。