Electroorganic Chemistry. XXVI. Electrooxidation of Enamines, Haloolefins, and Enol Ethers

Abstract Electrooxidation of enamines in methanol afforded two types of methoxylated enamines. Similar treatment of enol ethers gave trimethoxylated compounds. The products formed by the electrolysis of haloolefins in acetic acid were α-acetoxy haloolefins and α-acetoxy ketones.