A Reversible Protection Strategy to Improve Fmoc-SPPS of Peptide Thioesters by the N-Acylurea Approach

Lignende værker

• Synthesis of protected norcysteines for SPPS compatible with Fmoc-strategy
  af: Samant, Manoj P., et al.
  Udgivet: (2007)
• An efficient Fmoc-SPPS approach for the generation of thioester peptide precursors for use in native chemical ligation
  af: Blanco-Canosa, Juan B., et al.
  Udgivet: (2008)
• Fmoc-Sec(Xan)-OH: Synthesis and Utility of Fmoc Selenocysteine SPPS Derivatives with Acid-Labile Sidechain Protection
  af: Flemer, Stevenson
  Udgivet: (2014)
• Efficient Chemical Protein Synthesis using Fmoc‐Masked N‐Terminal Cysteine in Peptide Thioester Segments
  af: Kar, Abhisek, et al.
  Udgivet: (2020)
• A straightforward method for automated Fmoc-based synthesis of bio-inspired peptide crypto-thioesters
  af: Terrier, Victor P., et al.
  Udgivet: (2016)