Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 1989, 54, 3360-3373
https://doi.org/10.1135/cccc19893360

Ammonolysis mediated side reactions of β-tert-butyl aspartyl peptides

István Schön and Attila Rill

Chemical Works of Gedeon Richter, Ltd., Lajos Kisfaludy Research Laboratory, H-1475 Budapest, P.O/ Box 27, Hungary

Crossref Cited-by Linking

  • Subirós‐Funosas Ramon, El‐Faham Ayman, Albericio Fernando: Use of Oxyma as pH modulatory agent to be used in the prevention of base‐driven side reactions and its effect on 2‐chlorotrityl chloride resin. Biopolymers 2012, 98, 89. <https://doi.org/10.1002/bip.21713>
  • Subirós-Funosas Ramon, El-Faham Ayman, Albericio Fernando: Aspartimide formation in peptide chemistry: occurrence, prevention strategies and the role of N-hydroxylamines. Tedrahedron 2011, 67, 8595. <https://doi.org/10.1016/j.tet.2011.08.046>
  • Radkiewicz Jennifer L., Zipse H., Clarke Steven, Houk K. N.: Accelerated Racemization of Aspartic Acid and Asparagine Residues via Succinimide Intermediates:  An ab Initio Theoretical Exploration of Mechanism. J. Am. Chem. Soc. 1996, 118, 9148. <https://doi.org/10.1021/ja953505b>
  • Schön István, Nyéki Olga: Unprecedented transformation of aspartyl peptides by conjugative degradation. J. Chem. Soc., Chem. Commun. 1994, 393. <https://doi.org/10.1039/C39940000393>
  • Dölling Rudolf, Beyermann Michael, Haenel Jügen, Kernchen Frank, Krause Eberhard, Franke Peter, Brudel Michael, Bienert Michael: Piperidine-mediated side product formation for Asp(OBut)-containing peptides. J. Chem. Soc., Chem. Commun. 1994, 853. <https://doi.org/10.1039/C39940000853>
  • Schön István, Szirtes Tamás, Rill Attila, Balogh Gábor, Vadász Zsolt, Seprődi János, Teplán István, Chino Naoyoshi, Kumogaye Kumiko Yoshizawa, Sakakibara Shumpei: Aspartate racemization in synthetic peptides. Part 2. Tendency to racemization of aminosuccinyl residue. J. Chem. Soc., Perkin Trans. 1 1991, 3213. <https://doi.org/10.1039/P19910003213>