A phosphine-free effective palladium catalyst for aqueous Suzuki-Miyaura Cross-Coupling.
The Suzuki reaction (sometimes to referred to as the Suzuki-Miyaura reaction or "Suzuki Coupling") is an organic reaction that is classified as a coupling reaction where the coupling partners are a boronic acid with a halide catalyzed by a palladium complex.
From the laboratory of Benjamin G. Davis, PhD, University of Oxford.
Part of The Investigator's Annexe program.
|Product Type:||Small Molecule|
|Molecular Weight:||478.71 kDa|
|Purity:||Pd: 10 mM; transition metal impurity <0.1 mM|
|Solubility:||Soluble in H2O|
|Comments:||10uL for protein reaction; 2.5mL for 0.25 mol aryl bromide|
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