“…Recently, incorporating a ferrocenyl group into peptide structures has received considerable attention [ 10 , 11 , 12 , 13 ] as ferrocene was extensively exploited as a potential probe to identify non-covalent interactions between peptide structures, and the electron-transfer properties of different peptide secondary units. Although versatile ferrocenyl peptides or peptide-like derivatives have been reported [ 2 , 14 , 15 , 16 , 17 , 18 , 19 ], the majority of such compounds were generally obtained via a time-consuming stepwise strategy, which is usually inefficient and reduces the overall greenness of the synthesis.…”