Reductive ligation mediated one-step disulfide formation of S-nitrosothiols.

Loading...
Thumbnail Image

Date

2010-09-17

Journal Title

Journal ISSN

Volume Title

Repository Usage Stats

245
views
184
downloads

Citation Stats

Abstract

A one-step reductive ligation mediated disulfide formation of S-nitrosothiols was developed. This reaction involves the reaction of the S-nitroso group with phosphine-thioesters to form sulfenamide and thiolate intermediates, which then undergo a fast intermolecular disulfide formation to form stable conjugates. This reaction can be used to design new biosensors of S-nitrosated proteins.

Department

Description

Provenance

Citation

Published Version (Please cite this version)

10.1021/ol101863s

Publication Info

Zhang, Jiming, Sheng Li, Dehui Zhang, Hua Wang, A Richard Whorton and Ming Xian (2010). Reductive ligation mediated one-step disulfide formation of S-nitrosothiols. Org Lett, 12(18). pp. 4208–4211. 10.1021/ol101863s Retrieved from https://hdl.handle.net/10161/4108.

This is constructed from limited available data and may be imprecise. To cite this article, please review & use the official citation provided by the journal.


Unless otherwise indicated, scholarly articles published by Duke faculty members are made available here with a CC-BY-NC (Creative Commons Attribution Non-Commercial) license, as enabled by the Duke Open Access Policy. If you wish to use the materials in ways not already permitted under CC-BY-NC, please consult the copyright owner. Other materials are made available here through the author’s grant of a non-exclusive license to make their work openly accessible.