Several 3-acylfurans 3 were prepared in excellent yield using a one-pot procedure involving the palladium-catalyzed cross-coupling of commercially available acid chlorides with tributyl(3-furyl)-stannane 2 at room temperature.
几种3-酰基
呋喃3通过一种一锅法制备, yield 良好,该方法涉及在室温下使用
钯催化的交叉偶联反应,将商业可得的酸
氯化物与三丁基(3-
呋喃基)
锡化物2结合。