Palladium Catalyzed Aerobic Oxidative Amination of Alkenes

Amines are widely applied in the chemical and pharmaceutical industries, and the development of synthetic methods for their preparation is driven by their importance. The amination of alkenes is a direct and efficient method for the construction of amines, of which oxidative amination is more valuable because it can give the desired products with greater functionality and flexibility. In oxidative amination, using molecular oxygen (O-2) as a terminal oxidant has promising industrial application prospects. In recent years, the palladium-catalyzed aerobic oxidation of alkenes has seen significant progress, and its related research has also been extended to the aerobic oxidative amination of alkenes. The corresponding oxidation systems have been developed from early research involving the introduction of cocatalysts to the more recent systems which utilize auxiliary ligands instead of cocatalysts. In this review, the advancements in the palladium-catalyzed aerobic oxidative amination of monoalkenes and conjugated dienes over the last two decades are discussed, with emphasis on aerobic oxidation process and their associated mechanisms.

Automated summary

Amines are widely used in the chemical and pharmaceutical industries, and research on synthetic methods for their preparation is driven by their importance. The amination of alkenes is a direct and efficient method for the construction of amines, with oxidative amination being more valuable due to its ability to produce products with greater functionality and flexibility. The use of molecular oxygen as a terminal oxidant in oxidative amination shows promising application prospects. Recent advancements in palladium-catalyzed aerobic oxidative amination of alkenes are discussed, with a focus on the oxidation process and associated mechanisms.