Yang Mao-Lin, Wu Xiao-Feng
Leibniz-Institut für Katalyse e.V. Albert-Einstein-Str. 29a 18059 Rostock Germany
Dalian National Laboratory for Clean Energy, Dalian Institute of Chemical Physics, Chinese Academy of Sciences 116023 Liaoning China.
Chem Sci. 2025 Aug 5;16(34):15676-15683. doi: 10.1039/d5sc04120a. eCollection 2025 Aug 27.
Regioselective transformation is among the long-standing challenges in organic synthesis, particularly involving gas trapping. We present here a novel photocatalytic strategy for the regioselective carbonylation reaction toward α-aminoketones. Experimental studies reveal that protonic acids dissociated from protonated amines facilitate the reactions of low-reactive aldehydes and enhance the electrophilicity of imines, thereby promoting the efficient coupling of less nucleophilic acyl radicals. This approach introduces a reliable framework for controlling regioselectivity in photocatalytic multi-radical-coupled CO trapping reactions, broadens the chemical space of α-aminoketones, and advances carbonylation reactions for sustainable development.
区域选择性转化是有机合成中长期存在的挑战之一,尤其是涉及气体捕获的情况。我们在此提出一种用于α-氨基酮区域选择性羰基化反应的新型光催化策略。实验研究表明,从质子化胺中解离出的质子酸促进了低反应活性醛的反应,并增强了亚胺的亲电性,从而促进了亲核性较低的酰基自由基的有效偶联。这种方法为光催化多自由基偶联CO捕获反应中的区域选择性控制引入了一个可靠的框架,拓宽了α-氨基酮的化学空间,并推动了羰基化反应的可持续发展。