Literature DB >> 35763672

Thiol Catalysis of Selenosulfide Bond Cleavage by a Triarylphosphine.

Olga Firstova1, Oleg Melnyk1, Vincent Diemer1.   

Abstract

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.

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Year:  2022        PMID: 35763672     DOI: 10.1021/acs.joc.2c00934

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.198


  1 in total

1.  Redox-Controlled Chemical Protein Synthesis: Sundry Shades of Latency.

Authors:  Vangelis Agouridas; Nathalie Ollivier; Jérôme Vicogne; Vincent Diemer; Oleg Melnyk
Journal:  Acc Chem Res       Date:  2022-09-09       Impact factor: 24.466

  1 in total

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