Synthesis of Constrained Tetracyclic Peptides by Consecutive CEPS, CLIPS, and Oxime Ligation
journal contributionposted on 26.03.2019 by Dieuwertje E. Streefkerk, Marcel Schmidt, Johannes H. Ippel, Tilman M. Hackeng, Timo Nuijens, Peter Timmerman, Jan H. van Maarseveen
Any type of content formally published in an academic journal, usually following a peer-review process.
In Nature, multicyclic peptides constitute a versatile molecule class with various biological functions. For their pharmaceutical exploitation, chemical methodologies that enable selective consecutive macrocyclizations are required. We disclose a combination of enzymatic macrocyclization, CLIPS alkylation, and oxime ligation to prepare tetracyclic peptides. Five new small molecular scaffolds and differently sized model peptides featuring noncanonical amino acids were synthesized. Enzymatic macrocyclization, followed by one-pot scaffold-assisted cyclizations, yielded 21 tetracyclic peptides in a facile and robust manner.