Catalytic Oligopeptide Synthesis

Abstract

Waste-free catalytic assembly of α-amino acids is fueled by a multiboron catalyst that features a characteristic B₃NO₂ heterocycle, providing a versatile catalytic protocol wherein functionalized natural α-amino acid units are accommodated and commonly used protecting groups are tolerated. The facile dehydrative conditions eliminate the use of engineered peptide coupling reagents, exemplifying a greener catalytic alternative for peptide coupling. The catalysis is sufficiently robust to enable pentapeptide synthesis, constructing all four amide bond linkages in a catalytic fashion.