Electrophotochemical Metal-Catalyzed Decarboxylative Coupling of Aliphatic Carboxylic Acids

被引:31
|
作者
Yang, Kai [1 ,3 ]
Lu, Jiaqing [1 ,2 ]
Li, Liubo [1 ]
Luo, Sanzhong [3 ]
Fu, Niankai [1 ,2 ]
机构
[1] Chinese Acad Sci, Inst Chem, CAS Key Lab Mol Recognit & Funct, Beijing Natl Lab Mol Sci, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Tsinghua Univ, Ctr Basic Mol Sci, Dept Chem, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
aliphatic carboxylic acids; decarboxylative functionalization; electrophotocatalysis; paired electrolysis; SINGLE-ELECTRON TRANSMETALATION; CROSS; PHOTOREDOX; OXIDATION; ARYLATION; ALCOHOLS; LIGHT; FUNCTIONALIZATION; REDUCTION; UNLOCKING;
D O I
10.1002/chem.202202370
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An electrophotochemical dual metal-catalyzed protocol for decarboxylative arylation of simple aliphatic carboxylic acids with aryl halides is reported. The relative stabilities of catalytically active metal complexes simultaneously generated at anode and cathode are the key design elements for the success of this convergent paired electrolysis. This new electrophotocatalytic method is mild, robust, and most importantly, capable of accommodating simple primary aliphatic acids including acetic acid - ubiquitous and variegated structural motifs yet remain oddly challenging substrates - directly as native functional groups for decarboxylative C(sp(2))-C(sp(3)) bond formation.
引用
收藏
页数:6
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