Unmasking latent thioesters under hydrophobic-compatible conditions

J Pept Sci. 2021 Nov;27(11):e3358. doi: 10.1002/psc.3358. Epub 2021 Jun 13.

Abstract

Hydrophobic latent C-terminal thioesters were converted into thioesters, and were also coupled with cysteine in one-pot reactions, using conditions generally compatible with hydrophobic materials. The reaction conditions (ethanethiol and triethylamine in a mixture of DMF and THF) are compatible with acid-labile protecting groups (Boc/t-Bu) that are standard in Fmoc peptide synthesis.

Keywords: chemoselective; hydrophobic; latent thioester; ligation; organic.

MeSH terms

  • Cysteine*
  • Peptides*

Substances

  • Peptides
  • Cysteine