Facile access to foldable redox-active flavin-peptide conjugates Stricker, Friedrich J Kölsch, Jonas Christopher Beil, Sebastian B. Preiß, Sebastian Waldvogel, Siegfried R. Opatz, Till Besenius, Pol ddc:540 A convenient approach for the synthesis of foldable redox-active flavin peptide conjugates was established. A model β-hairpin oligopeptide motif was utilized to demonstrate that azidolysine side-chains are readily functionalised with an alkyne-bearing flavine derivative. The folding equilibrium of the peptide backbone as well as the redox behaviour of the flavin moieties remains intact after the conjugation. Royal Society of Chemistry 2021 info:eu-repo/semantics/article doc-type:article text http://purl.org/coar/resource_type/c_2df8fbb1 https://research-explorer.ista.ac.at/record/21808 Stricker FJ, Kölsch JC, Beil SB, et al. Facile access to foldable redox-active flavin-peptide conjugates. <i>Organic &#38; Biomolecular Chemistry</i>. 2021;19(20):4483-4486. doi:<a href="https://doi.org/10.1039/d1ob00414j">10.1039/d1ob00414j</a> eng info:eu-repo/semantics/altIdentifier/doi/10.1039/d1ob00414j info:eu-repo/semantics/altIdentifier/issn/1477-0520 info:eu-repo/semantics/altIdentifier/e-issn/1477-0539 info:eu-repo/semantics/altIdentifier/pmid/33960997 info:eu-repo/semantics/closedAccess