当前位置:
X-MOL 学术
›
Angew. Chem. Int. Ed.
›
论文详情
Our official English website, www.x-mol.net, welcomes your
feedback! (Note: you will need to create a separate account there.)
Electrochemical Ni-Catalyzed Decarboxylative C(sp3)−N Cross-Electrophile Coupling
Angewandte Chemie International Edition ( IF 16.1 ) Pub Date : 2024-02-01 , DOI: 10.1002/anie.202315222
Yue-Ming Cai 1 , Xiao-Ting Liu 1 , Lin-Lin Xu 1 , Ming Shang 1
Angewandte Chemie International Edition ( IF 16.1 ) Pub Date : 2024-02-01 , DOI: 10.1002/anie.202315222
Yue-Ming Cai 1 , Xiao-Ting Liu 1 , Lin-Lin Xu 1 , Ming Shang 1
Affiliation
![]() |
Ni-catalyzed decarboxylative C(sp3)−N cross-coupling of redox active ester and oxime esters was realized through electrochemical cathodic reduction. Mechanistic studies unveil a high-valent nickel species-driven reductive elimination pathway, rather than direct radical-radical coupling. The utility of this methodology was demonstrated through a broad scope (1°, 2°, 3° carboxylic acids) and late-stage functionalization of complex molecules.
中文翻译:
电化学 Ni 催化脱羧 C(sp3)−N 交叉电偶联
通过电化学阴极还原实现了氧化还原活性酯和肟酯的镍催化脱羧C(sp 3 )−N交叉偶联。机理研究揭示了高价镍物质驱动的还原消除途径,而不是直接的自由基-自由基耦合。该方法的实用性通过复杂分子的广泛范围(1°、2°、3°羧酸)和后期功能化得到了证明。
更新日期:2024-02-01
中文翻译:

电化学 Ni 催化脱羧 C(sp3)−N 交叉电偶联
通过电化学阴极还原实现了氧化还原活性酯和肟酯的镍催化脱羧C(sp 3 )−N交叉偶联。机理研究揭示了高价镍物质驱动的还原消除途径,而不是直接的自由基-自由基耦合。该方法的实用性通过复杂分子的广泛范围(1°、2°、3°羧酸)和后期功能化得到了证明。