Login / Signup

Thiol Catalysis of Selenosulfide Bond Cleavage by a Triarylphosphine.

Olga FirstovaOleg MelnykVincent Diemer
Published in: The Journal of organic chemistry (2022)
The arylthiol 4-mercaptophenylacetic acid (MPAA) is a powerful catalyst of selenosulfide bond reduction by the triarylphosphine 3,3',3″-phosphanetriyltris(benzenesulfonic acid) trisodium salt (TPPTS). Both reagents are water-soluble at neutral pH and are particularly adapted for working with unprotected peptidic substrates. Contrary to trialkylphosphines such as tris(2-carboxyethyl)phosphine hydrochloride (TCEP), TPPTS has the advantage of not inducing deselenization reactions. We believe that the work reported here will be of value for those manipulating selenosulfide bonds in peptidic or protein molecules.
Keyphrases
  • water soluble
  • transition metal
  • ionic liquid
  • room temperature
  • protein protein
  • dna binding
  • amino acid
  • small molecule
  • transcription factor
  • reduced graphene oxide