Nitrogen Arylation for Macrocyclization of Unprotected Peptides.

ABSTRACT: We describe an efficient and mild method for the synthesis of macrocyclic peptides via nitrogen arylation from unprotected precursors. Various electrophiles and lysine-based nucleophiles were investigated and showed high-yielding product formation, even for a macrocyclization scan with 14 variants. We found that nitrogen-linked aryl products were more stable to base and oxidation when compared to thiol arylated species, thereby highlighting the utility of this methodology. Finally, N-aryl macrocyclization was performed on a p53 peptide inhibitor of MDM2 and resulted in identification of a nanomolar binder with improved proteolytic stability and cell permeability.

SUBMITTER: Lautrette G 

PROVIDER: S-EPMC6150454 | biostudies-other | 2016 Jul

REPOSITORIES: biostudies-other