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Arginine side-chain modification that occurs during copper-catalysed azide–alkyne click reactions resembles an advanced glycation end product. Anne C. Conibear, Karine Farbiarz, Rupert L. Mayer, Maria Matveenko, Hanspeter Kählig, Christian F. W. Becker , Org. Biomol. Chem. , 2016 , 14 , 6205

An efficient one-pot conversion of carboxylic acids into benzimidazoles via an HBTU-promoted methodology. Leonard Barasa, Sabesan Yoganathan , RSC Adv. , 2018 , 8 , 35824

E3 ligase ligand chemistries: from building blocks to protein degraders. Izidor Sosič, Aleša Bricelj, Christian Steinebach , Chem. Soc. Rev. , 2022 , 51 , 3487

Synthesis of peptides analogous to the N-terminal eicosapeptide sequence of ribonuclease A. Part I. Synthesis of the orn¹⁰-hexapeptide analogue of the sequence 7–12. Fernando Marchiori, Raniero Rocchi, Giorgio Vidali, Antonmario Tamburro, Ernesto Scoffone , J. Chem. Soc. C , 1967 , 81

Anion transport properties of amine and amide-sidechained peptides are affected by charge and phospholipid composition. Lei You, Ruiqiong Li, George W. Gokel , Org. Biomol. Chem. , 2008 , 6 , 2914

Amide protection and amide supports in solid-phase peptide synthesis. P. G. Pietta, Garland R. Marshall , J. Chem. Soc. D , 1970 , 650

Total synthesis of urogastrone (human epidermal growth factor, h-EGF). Part 1. Synthesis of the fully protected urogastrone. Masahiro Neya, Daijiro Hagiwara, Yoshio Miyazaki, Takashi Nakamura, Keiji Hemmi, Masashi Hashimoto , J. Chem. Soc., Perkin Trans. 1 , 1989 , 2187

New reaction conditions using trifluoroethanol for the E-I Hofmann rearrangement. Yoshihiro Matsumura, Yuki Satoh, Kimihiro Shirai, Osamu Onomura, Toshihide Maki , J. Chem. Soc., Perkin Trans. 1 , 1999 , 2057

Formation of by-products during sodium–liquid ammonia reduction in peptide chemistry. István Schőn, Tamás Szirtes, Tamás Überhardt , J. Chem. Soc., Chem. Commun. , 1982 , 639

Kinetic resolution of esters via metal catalyzed methanolysis reactions. Christopher I. Maxwell, Kalpa Shah, Pavel V. Samuleev, Alexei A. Neverov, R. Stan Brown , Org. Biomol. Chem. , 2008 , 6 , 2796