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Thiol Catalysis of Selenosulfide Bond Cleavage by a Triarylphosphine.
- 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