Here the aromatic formylation mediated by TiCl4 and dichloromethyl methyl ether previously described by our group has been explored for a wide range of aromatic rings, including phenols, methoxy- and methylbenzenes, as an excellent way to produce aromatic aldehydes. Here we determine that the regioselectivity of this process is highly promoted by the coordination between the atoms present in the aromatic moiety and those in the metal core.
在这里,我们探索了我们小组之前描述的由TiCl4和二
氯甲基
甲醚介导的芳香环的甲酰化反应,适用于广泛类型的芳香环,包括
酚、
甲氧基苯和甲基苯,作为生成芳香醛的一种优秀方法。在此,我们确定该过程的区域选择性高度受到芳香部分中存在的原子与
金属核中原子之间的配位作用促进。