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Synthesis
DOI: 10.1055/a-2756-7473
DOI: 10.1055/a-2756-7473
Paper
Published as part of the Special Topic 22nd International Symposium on Organometallic
Chemistry Directed Towards Organic Synthesis (OMCOS-22)
Epimerization-Free Synthesis of Azo-Substituted Di- and Tripeptides by Cross-Coupling of O-Triflated Derivatives and Diazenyl Anion Equivalents
Authors
This research was supported by the Fonds der Chemischen Industrie (predoctoral fellowship to W.O., 2024–2027). M.O. is indebted to the Einstein Foundation Berlin for an endowed professorship.

Abstract
Based on our previous work, a method for the synthesis of azo-substituted small peptides through C(sp2)–N(sp2) cross-coupling between triflated peptide derivatives and N-aryl-N′-trimethylsilyldiazenes is reported. The peptide-substituted azobenzene products are formed in acceptable yields with full stereoretention at the asymmetrically substituted carbon atom despite the basic reaction medium.
Keywords
Azobenzenes - C–N cross-coupling - Late-stage peptide modification - Palladium - Photoswitchable peptidesPublication History
Received: 01 November 2025
Accepted after revision: 26 November 2025
Accepted Manuscript online:
26 November 2025
Article published online:
14 January 2026
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References
- 1a Malins LR. Curr Opin Chem Biol 2018; 46: 25
- 1b Tong HR, Li B, Li G, He G, Chen G. CCS Chem 2021; 3: 1797
- 1c Hu JJ, He PY, Li YMJ. Pep Sci 2021; 27: e3286
- 1d Boto A, González CC, Hernándes D, Romero-Estudillo I, Saavedra CJ. Org Chem Front 2021; 8: 6720
- 1e Bhunia S, Purushotham M, Karan G, Paul B, Maji MS. Synthesis 2023; 55: 3701
- 2a Mart RJ, Allemann RK. Chem Commun 2016; 52: 12262
- 2b Albert L, Vázquez O. Chem Commun 2019; 55: 10192
- 2c Erdei E, Marcos JT, Varró N, Horváti K, Bacsa B, Mándity IM. Br J Pharmacol 2025; 182: 4458
- 3a Wang P, Cheng Y, Wu C. et al. Org Lett 2021; 23: 4137
- 3b Sharma S, Naldrett MJ, Gill MJ, Checco JW. J Am Chem Soc 2024; 146: 13676
- 3c Bertolini M, Mendive-Tapia L, Ghashghaei O. et al. ACS Cent Sci 2024; 10: 969
- 3d Addy PS, Erickson SB, Italia JS, Chatterjee A. J Am Chem Soc 2017; 139: 11670
- 3e Addy PS, Zheng Y, Italia JS, Chatterjee A. ChemBioChem 2019; 20: 1659
- 4a Finck L, Oestreich M. Angew Chem Int Ed 2022; 61: e202210907
- 4b Finck L, Dabrowski S, Oestreich M. Synthesis 2023; 55: 1764
- 4c See also: Zhang K, Oestreich M. J Am Chem Soc 2025; 147: 32329
- 5a Chauvier C, Finck L, Hecht S, Oestreich M. Organometallics 2019; 38: 4679
- 5b Finck L, Oestreich M. J Org Chem 2023; 88: 15531
- 6a Li X, Qi L, Li B, Zhao Z, He G, Chen G. Org Lett 2020; 22: 6209
- 6b Guo P, Wang K, Jin WJ. et al. J Am Chem Soc 2021; 143: 513
- 6c Chen H, Mao R, Brzozowski M, Nguyen NH, Sleebs BE. Org Lett 2021; 23: 4244
- 6d Sharninghausen LS, Preshlock S, Joy ST. et al. J Am Chem Soc 2022; 144: 7422
- 6e Willemse T, Schepens W, van Vlijmen HWT, Maes BUW, Ballet S. Catalysts 2017; 7: 74
- 7a Prieto M, Mayor S, Rodríguez K, Lloyd-Williams P, Giralt E. J Org Chem 2007; 72: 1047
- 7b Prieto M, Mayor S, Lloyd-Williams P, Giralt E. J Org Chem 2009; 74: 9202
- 8 Duan J, Du YF, Pang X, Shu XZ. Chem Sci 2019; 10: 8706
- 9 Ousmer M, Braun NA, Bavoux C, Perrin M, Ciufolini MA. J Am Chem Soc 2001; 123: 7534
- 10 Wang A, Cui L, Debnath S. et al. ACS Appl Mater Interfaces 2017; 9: 21390
- 11 Nudelman A, Bechor Y, Falb E, Fischer B, Wexler BA, Nudelman A. Synth Commun 1998; 28: 471
For reviews on the late-stage modification of peptides, see:
For recent examples for the diazenylation of tyrosine residues in peptides and proteins, see:
For recent examples for the diazenylation of 5-hydroxy-tryptophane residues in peptides, see:
For their preparation, see:
For a general review, see:
For recent examples for the modification of (pseudo)halogenated tyrosine and phenylalanine residues in peptides through palladium-catalyzed cross-coupling reactions, see:
For a review on peptide diversification by Suzuki–Miyaura cross-coupling, see:
Racemization has also been documented for the Suzuki–Miyaura cross-coupling of tyrosine derivatives: