Zhao Fengqian, Ai Han-Jun, Wu Xiao-Feng
Leibniz-Institut für Katalyse e.V., Albert-Einstein-Straße 29a, 18059, Rostock, Germany.
Dalian National Laboratory for Clean Energy, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 116023, Dalian, Liaoning, China.
Angew Chem Int Ed Engl. 2022 Apr 19;61(17):e202200062. doi: 10.1002/anie.202200062. Epub 2022 Feb 26.
Controllable production of α-keto amides and amides from the same substrates is an attractive goal in the field of transition-metal-catalyzed (double-)carbonylation. Herein, a novel copper-catalyzed highly selective double carbonylation of alkyl bromides has been developed. Moderate to good yields of α-keto amides were obtained as the only products. In the case of alkyl iodides, double- and mono-carbonylation can be achieved controllably under different conditions.
在过渡金属催化的(双)羰基化领域,从相同底物可控地生产α-酮酰胺和酰胺是一个具有吸引力的目标。在此,我们开发了一种新型的铜催化的溴代烷烃高选择性双羰基化反应。以中等至良好的产率得到了仅有的产物α-酮酰胺。对于碘代烷烃,在不同条件下可以可控地实现双羰基化和单羰基化。