Related Experiment Video
Updated: Jan 20, 2026

Constructing Cyclic Peptides Using an On-Tether Sulfonium Center
Published on: September 28, 2022
Site-Selective C-H Oxygenation via Aryl Sulfonium Salts
Ruocheng Sang1, Stamatis E Korkis1, Wanqi Su1
1Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, 45470, Mülheim an der Ruhr, Germany.
Abstract:
Herein, we report a two-step process forming arene C-O bonds in excellent site-selectivity at a late-stage. The C-O bond formation is achieved by selective introduction of a thianthrenium group, which is then converted into C-O bonds using photoredox chemistry. Electron-rich, -poor and -neutral arenes as well as complex drug-like small molecules are successfully transformed into both phenols and various ethers. The sequence differs conceptually from all previous arene oxygenation reactions in that oxygen functionality can be incorporated into complex small molecules at a late stage site-selectively, which has not been shown via aryl halides.
Related Concept Videos
07:11Constructing Cyclic Peptides Using an On-Tether Sulfonium Center
Determining the pH of Salt Solutions
Responses to Salt Stress
Nomenclature of Aryl and Heterocyclic Amines
05:07Microwave-Assisted Preparation of 1-Aryl-1H-pyrazole-5-amines
08:27Analysis of Effect of Compound Salt Stress on Seed Germination and Salt Tolerance Analysis of Pepper (Capsicum annuum L.)

