Related Experiment Video
Updated: Jan 20, 2026

Constructing Cyclic Peptides Using an On-Tether Sulfonium Center
Published on: September 28, 2022
C-N Cross-Couplings for Site-Selective Late-Stage Diversification via Aryl Sulfonium Salts
Pascal S Engl1, Andreas P Häring1, Florian Berger1
1Max-Planck-Institut für Kohlenforschung , Kaiser-Wilhelm Platz 1 , D-45470 Mülheim an der Ruhr , Germany.
Abstract:
We report diverse C-N cross-coupling reactions of aryl thianthrenium salts that are formed site-selectively by direct C-H functionalization. The scope of N-nucleophiles ranges from primary and secondary alkyl and aryl amines to various N-containing heterocycles, and the overall transformation is applicable to late-stage functionalization of complex, drug-like small molecules.
Related Concept Videos
Aryldiazonium Salts to Azo Dyes: Diazo Coupling
Determining the pH of Salt Solutions
Responses to Salt Stress
Crossing Over
The homologous pairs of sister chromosomes—one from the maternal and one from the paternal genome—then begin to align alongside each other lengthwise, matching corresponding DNA positions in a process...
Crossing Over
Nomenclature of Aryl and Heterocyclic Amines

