Synthesis of cyclic, multivalent Arg-Gly-Asp using sequential thiol–ene/thiol–yne photoreactions

Abstract

A unique method has been developed for the formation of multivalent cyclic peptides. This procedure exploits on-resin peptide cyclization using a photoinitiated thiol–ene click reaction and subsequent clustering using thiol–yne photochemistry. Both reactions utilize the sulfhydryl group on natural cysteine amino acids to participate in the thiol-mediated reactions.