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. Author manuscript; available in PMC: 2022 Jul 29.
Published in final edited form as: Angew Chem Int Ed Engl. 2022 Mar 2;61(18):e202116999. doi: 10.1002/anie.202116999

Figure 1:

Figure 1:

Assessment of PICCO macrocyclization. (A) Beads displaying a linker capped with Cys-STmp and an oxazole (Compound 1a) were subjected to three rounds of amination and acylation to generate a linear PICCO (Compound 2). Cysteine deprotection allows thioether formation, generating the macrocycle (Compound 3). (B) LC/MS analysis demonstrates complete cyclization of the linear precursor. See supporting information (Fig. S2) for complete characterization.