Expert guidance for catalyst selection across major reaction classes. Navigate the complexity of modern catalysis with our comprehensive technical resources and application notes.
Reduction of C=C, C=O, C=N, aromatics, and nitro groups. Catalyst selection for Pd, Pt, Ru, Rh, and Ni systems under diverse conditions.
Suzuki, Heck, Negishi, Stille, and Buchwald-Hartwig reactions. Palladium catalysts and ligand optimization for challenging substrates.
Selective oxidation of alcohols, aldehydes, and C-H bonds. Catalytic systems for aerobic oxidation and peroxide-mediated transformations.
Aldol, Michael additions, and cycloadditions. Organocatalysts and metal complexes for stereoselective carbon framework construction.
Enantioselective reduction with chiral catalysts. BINAP, DuPhos, Josiphos systems for pharmaceutical intermediates with >99% ee.
Direct functionalization of C-H bonds. Pd, Rh, Ir, and Ru catalysts for arylation, alkylation, and borylation reactions.
Reduction using hydrogen donors instead of H2 gas. Safer alternative for ketone and imine reduction using isopropanol or formic acid.
Olefin cross-metathesis, ring-closing, and ring-opening metathesis polymerization. Grubbs and Hoveyda-Grubbs catalyst systems.
Incorporation of CO into organic molecules. Hydroformylation, carbonylative coupling, and Monsanto/Cativa acetic acid processes.
Enzyme-catalyzed transformations for green chemistry. Ketoreductases, transaminases, and hydrolases for pharmaceutical synthesis.
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