Photoredox Ni-catalyzed peptide C(sp²)-O cross-coupling: from intermolecular reactions to side chain-to-tail macrocyclization.

ABSTRACT: Ni/photoredox (4DPAIPN) dual catalysis enabled challenging peptide C(sp²)-O coupling reactions. Successful cross-coupling reactions were demonstrated with highly functionalized alcohols including side chains of amino acids (i.e., serine, threonine, tyrosine), trans-4-hydroxy-l-proline, alkyl alcohols, alkynylated alcohols, and carbohydrates. Coupling reactions between bromobenzoyl-capped peptides containing various side chains and either a protected serine building block or a serine-containing dipeptide also proceeded efficiently. Chemoselective C-O coupling (over C-N) was achieved in intermolecular reactions in the presence of a C-terminal primary amide. Furthermore, by judicious structural design in combination with computational modeling, we demonstrated side chain-to-tail macrocyclization of peptides containing a ?-turn motif via C-O coupling. The methodology developed in this work brings new opportunities for late-stage diversification of complex linear and macrocyclic peptides.

SUBMITTER: Lee H 

PROVIDER: S-EPMC6524625 | biostudies-literature | 2019 May

REPOSITORIES: biostudies-literature