Login / Signup

Chemoselective Synthesis of N-Terminal Cysteinyl Thioesters via β,γ-C,S Thiol-Michael Addition.

Rita PetraccaKatherine A BowenLauren McSweeneySiobhan O'FlahertyVito GennaBrendan TwamleyMarc DevocelleEoin M Scanlan
Published in: Organic letters (2019)
Dehydroalanine (ΔAla) is a highly electrophilic residue that can react efficiently with sulfur nucleophiles to furnish cysteinyl analogues. Herein, we report an efficient synthesis of N-terminal cysteinyl thioesters, suitable for S, N-acyl transfer, based on β,γ-C,S thiol-Michael addition. Both ionic and radical-based methodologies were found to be efficient for this process.
Keyphrases
  • molecular docking
  • fatty acid
  • ionic liquid
  • amino acid
  • molecular dynamics simulations
  • structure activity relationship