Oxamic acids: useful precursors of carbamoyl radicals
Ikechukwu Martin Ogbu, Gülbin Kurtay, Frédéric Robert, Yannick Landais
Abstract
This review article describes the recent development in the chemistry of carbamoyl radicals generated from oxamic acids. This mild and efficient method compares well with previous methods of generation of these nucleophilic radicals. The oxidative decarboxylation of oxamic acids can be mediated through thermal, photochemical, electrochemical or photoelectrochemical means, generating carbamoyl radicals, which may further add to unsaturated systems to provide a broad range of important amides. Oxidative decarboxylation of oxamic acids also offers a straightforward entry for the preparation of urethanes, ureas, and thioureas.
Topics & Concepts
ChemistryRadicalNucleophileDecarboxylationOxidative decarboxylationOxidative phosphorylationNucleophilic additionOrganic chemistryPhotochemistryBiochemistryCatalysisRadical Photochemical ReactionsSulfur-Based Synthesis TechniquesCatalytic C–H Functionalization Methods