†College of Chemical Engineering, Xiangtan University, Xiangtan 411105, China.
‡State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Xue Yuan Road 38, Beijing 100191, China.
Org Lett. 2015 May 15;17(10):2542-5. doi: 10.1021/acs.orglett.5b01114. Epub 2015 May 7.
A unique copper-catalyzed aerobic oxidative C-C bond cleavage of simple unstrained ketones with air and amines has been developed. In this chemistry, amides and oxo amides are easily synthesized through the selective C-C bond cleavage of simple ketones or unstrained cycloketones. The broad substrate scopes and use of an inexpensive copper catalyst and green molecular oxygen as an oxidant as well as an O-source make this protocol very attractive for potential synthetic applications. The control experiments reveal that the present copper-catalyzed oxidative C-C bond cleavage of simple ketones proceeds in a novel catalytic pathway rather than through the cleavage of a dioxetane intermediate.
一种独特的铜催化有氧氧化 C-C 键断裂反应,可实现简单无张力酮类化合物与空气和胺类的反应。在这种化学中,酰胺和氧代酰胺可以通过简单酮类化合物或无张力环酮的选择性 C-C 键断裂轻松合成。广泛的底物范围、使用廉价的铜催化剂和绿色分子氧作为氧化剂以及 O 源,使得该方法非常有吸引力,具有潜在的合成应用价值。控制实验表明,目前的铜催化简单酮类化合物的氧化 C-C 键断裂反应是通过一种新的催化途径进行的,而不是通过二氧戊环中间体的断裂。