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[DPPB RuCl₂ AMPY], Baratta's Catalyst | CAS Number: 850424-32-7
CAS Number: 3375-31-3 | Pd(OAc)2
[RockPhos Pd(allyl)]OTf | CAS Number: 1798782-31-6
[Me₃OMetBuXPhos Pd(allyl)]OTf | CAS Number: 2924017-86-5
Bis(tri-tert-butylphosphine)palladium(0) | CAS Number: 2548904-17-0
PdCl₂ (dippf) | CAS Number: 215788-65-1
[Me₄tBuXPhos Pd(allyl)]OTf | CAS Number: 1798782-29-2
Aromatic and aliphatic primary amines can be obtained using our Transaminases
GDH enzymes catalyses the oxidation of D-glucose to D-glucolactone, while reducing in turn NAD+ or NADP+ to NADH and NADPH.
Triflate and chloride pi-allyl palladium products
Second and third generation buchwald precatalysts for advanced cross-coupling applications.
Bis-phosphine palladium halide pre-catalysts for basic cross coupling applications.
Bisphosphonium dichloropalladate complexes featuring tertiary phosphonium ligands
ADH enzymes used to catalyse the reduction of ketones and aldehydes to the corresponding alcohols
Imine reductases (IREDs) biocatalysts are used to produce enantiopure primary, secondary and tertiary amines
Glucose dehydrogenase catalyses the oxidation of D-glucose to D-glucolactone
Formate dehydrogenase (FDH enzyme) oxidises formate to carbon dioxide
Ene reductase enzyme catalyse the reduction of C=C double bonds
Transaminase enzymes can be used to produce aromatic and aliphatic primary amines.
Alanine dehydrogenase catalyses the reductive amination of pyruvate to L-alanine
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