| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 68415 | Journal of Molecular Catalysis A: Chemical | 2006 | 4 Pages |
Abstract
A robust palladium catalyst system supported by the hybrid ligand N-heterocyclic carbene along with a phosphine derived from ferrocene has been discovered for the Suzuki cross-coupling reaction. This novel system effectively catalyzes the cross-coupling of aryl bromides and phenylboronic acid with up to 20,000 TONs and 10,000 h−1 TOFs to produce biaryl products in excellent yields.
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Related Topics
Physical Sciences and Engineering
Chemical Engineering
Catalysis
Authors
Ji-Cheng Shi, Peng-Yu Yang, Qingsong Tong, Yang Wu, Yiru Peng,