In the presence of 2-amino-2-phenylpropanoate salt (2a or 2e) as the amine source, aromatic aldehydes underwent decarboxylative transamination under very mild conditions to produce a variety of arylmethylamines in 44–99% yields. The work has provided an efficient new method for the synthesis of primary arylmethylamines.
在 2-
氨基-
2-苯基丙酸盐(2a或2e)作为胺源存在的情况下,芳香醛在非常温和的条件下进行脱羧
氨基转移,以 44-99% 的收率生产各种芳基
甲胺。该工作为伯芳基
甲胺的合成提供了一种高效的新方法。