Aqueous Palladium Catalyst

A phosphine-free effective palladium catalyst for aqueous Suzuki-Miyaura Cross-Coupling.

Highlights:

  • Ready to use (liquid form), no sample preparation needed
  • Allows for the mild coupling between aryl-boronic acids and substrates from small molecules, peptides, proteins and modified cell surface

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.

The Investigator's Annexe Part of The Investigator's Annexe program.

Catalog Number Product Size AVAILABILITY Price Qty
EOX102
Aqueous Palladium Catalyst
10mM Solution In stock
Regular Price:$161.00
Specifications

Product Type: Small Molecule
Name: Bis(2-amino-4,6-dihydroxypyrimidine)palladium(II) diacetate
Chemical Formula: C12H16N6O8Pd
Molecular Weight: 478.71 kDa
Format: Orange solution
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
Storage: Room temperature
Shipped: Ambient temperature

Provider
From the laboratory of Benjamin G. Davis, PhD, University of Oxford.
References
  1. Chalker JM, Wood CS, Davis BG. A convenient catalyst for aqueous and protein Suzuki-Miyaura cross-coupling. J. Am. Chem. Soc. 2009, 131, 16346–16347.

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