| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5275659 | Tetrahedron Letters | 2009 | 4 Pages |
Abstract
A simple and efficient procedure for Suzuki coupling of aryl bromides/iodides with aryl- and alkylboronic acids catalyzed by in situ-generated palladium(0) nanoparticles in water without any ligand in open air to produce a variety of functionalized biaryls and alkyl-aryls has been developed. The boronic acids act here as the reducing agent for the formation of Pd nanoparticles. The reactions are remarkably fast (5Â min) and high yielding. The catalyst is recyclable up to three runs without loss of efficiency.
Graphical abstractDownload full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Debasree Saha, Kalicharan Chattopadhyay, Brindaban C. Ranu,