Stereoselective diversificatio... Note

Stereoselective diversification of α-amino acids enabled by N-heterocyclic carbene catalysis

Chiral α-amino acids, essential to biological systems and drug design, drive demand for precise synthetic methods to access unnatural variants (UAAs) and stereochemically defined peptides. We report an N-heterocyclic-carbene-catalyzed strategy enabling enantioselective synthesis of α-(U)AA esters and peptides.