Chalcogen-Bonding-Enabled, Light-Driven Decarboxylative Oxygenation of Amino Acid Derivatives and Short Peptides...

Here we report a photocatalytic method for the decarboxylative oxygenation of amino acid derivatives and short peptides using dioxygen as a green oxidant. A reverse catalytic strategy utilizing Lewis basic diphenyl diselenide as a Lewis acid catalyst to activate carboxylic acid via chalcogen bonding interaction is the key to this work. This synthetic method is tolerant of functionalities present in both natural and non-proteinogenic amino acids, enabling the efficient synthesis of C-terminal amides or imides. Mechanistic studies suggest there is a dual noncovalent interaction between diphenyl diselenide and carboxylic acid, which allows radical decarboxylation through photoinduced intermolecular electron transfer. This new activation mode of carboxylic acids will add a new dimension to classical decarboxylative reactions.