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Thiol Catalysis of Selenosulfide Bond Cleavage by a Triarylphosphine.

Authors :
Firstova O
Melnyk O
Diemer V
Source :
The Journal of organic chemistry [J Org Chem] 2022 Jul 15; Vol. 87 (14), pp. 9426-9430. Date of Electronic Publication: 2022 Jun 28.
Publication Year :
2022

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.

Details

Language :
English
ISSN :
1520-6904
Volume :
87
Issue :
14
Database :
MEDLINE
Journal :
The Journal of organic chemistry
Publication Type :
Academic Journal
Accession number :
35763672
Full Text :
https://doi.org/10.1021/acs.joc.2c00934