作者: Ryan Sword , Steven O'Sullivan , John A. Murphy
DOI: 10.1071/CH12480
关键词: Green chemistry 、 Reactivity (chemistry) 、 Electrochemistry 、 Reaction mechanism 、 Medicinal chemistry 、 Sodium amalgam 、 Electron donor 、 Organic chemistry 、 Ionic liquid 、 Chemistry 、 Biocatalysis
摘要: We report the reactivity of an electron donor derived from N-methylisatin on reduction by sodium amalgam. Transfer a clear supernatant solution to iodoarenes affords products two-electron reduction. Reductions sulfones, activated arenesulfonamides, and Weinreb amides are also reported.