A Versatile System of Solvent, Catalyst, and Ligand for Challenging Biphenyl Synthesis Through Suzuki‐Miyaura Reactions
Suzuki-Miyaura cross-coupling reactions are difficult when both reaction partners (boronic acid and halide) are electron-poor. We describe here a system of solvent, catalyst, and ligand with which also electron-poor substrates react, without the necessity to try several conditions. The system consists of N-methylpyrrolidone as solvent, tris(dibenzylidenaceton)dipalladium(0) as catalyst, CuI as cocatalyst, and Davephos as ligand. This combination yields little or no Ullmann product, and the desired cross-coupling product is in moderate to excellent yields.
Authors
- Detlef Gabel (ORCID: https://orcid.org/0000-0002-8003-5080)
- Mahmoud K. Al‐Joumhawy (ORCID: https://orcid.org/0000-0001-9116-3398)
- Jui‐Chi Chang (ORCID: https://orcid.org/0000-0002-5384-3373)
Institutions
- University of Bremen (DE)
- Constructor University (DE)
- Yarmouk University (JO)
Publication Details
- Journal
- Chemistry - A European Journal
- Published
- 2025-11-26
- DOI
- https://doi.org/10.1002/chem.202501789
- Citations
- 1
- Primary Topic
- Catalytic Cross-Coupling Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.94
Funders
- Deutsche Forschungsgemeinschaft