| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5223193 | Tetrahedron | 2009 | 4 Pages |
Abstract
Copper chloride-catalyzed S-arylation of arenethiols is effected with activated aryl chlorides in neat water by using ethylenediamine as the pair ligand/base. This convenient, environmentally more friendly procedure for the coupling of aryl chlorides allows the arylation between sterically demanding coupling partners.
Graphical abstractCopper chloride-catalyzed S-arylation of arenethiols is effected with activated aryl chlorides in water by using ethylenediamine as the pair ligand/base.Download full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
MarÃa Teresa Herrero, Raul SanMartin, Esther DomÃnguez,