Visible Light-Mediated Deoxygenation Protocol for Synthesis of Dipeptide, Amide and Ester without Racemization

A green and sustainable visible light-induced triphenylphosphine-promoted deoxygenation strategy to generate acyl radicals from commercially available amino acids has been developed. A wide range of dipeptides, amides and esters were obtained in good yields (77-94%) without epimerization. The strategy has advantages of short reaction time, not requiring dry solvent or inert atmosphere, operationally simple conditions, broad substrate scope, good functionals tolerance.

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