Iron-Catalyzed, Light-Driven Decarboxylative Alkoxyamination

被引:5
|
作者
Innocent, Milan [1 ]
Tanguy, Clement [1 ]
Gavelle, Sigrid [1 ]
Aubineau, Thomas [1 ]
Guerinot, Amandine [1 ]
机构
[1] CNRS, ESPCI Paris PSL, Mol Macromol Chem & Mat, 10 Rue Vauquelin, F-75005 Paris, France
关键词
iron; photocatalysis; decarboxylation; LMCT; alkoxyamination; C-H ACTIVATION; CARBOXYLIC-ACIDS; CHARGE-TRANSFER; OXIDATION; RADICALS; CLEAVAGE; BIOMASS; LIGAND; TEMPO; OXYAMINATION;
D O I
10.1002/chem.202401252
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An iron-catalyzed visible-light driven decarboxylative alkoxyamination is disclosed. In the presence of FeBr2 and TEMPO, a large array of carboxylic acids including marketed drugs and biobased molecules is turned into the corresponding alkoxyamine derivatives. The versatility of the latter offers an entry towards molecular diversity generation from abundant starting materials and catalyst. Overall, this method proposes a unified and general approach for LMCT-based iron-catalyzed decarboxylative functionalization. An iron-catalyzed, visible-light induced decarboxylative alkoxyamination of carboxylic acids with TEMPO is disclosed. In the presence of FeBr2 and TEMPO, a large array of carboxylic acids including marketed drugs and biobased molecules is turned into the corresponding alkoxyamine derivatives. The versatility of the latter offers an entry towards molecular diversity generation from abundant starting materials and catalyst. Overall, this method proposes a unified and general approach for LMCT-based iron-catalyzed decarboxylative functionalization. image
引用
收藏
页数:8
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