Publication | Closed Access
A General and Efficient Method for the Formylation of Aryl and Heteroaryl Bromides
214
Citations
42
References
2005
Year
Cross-coupling ReactionEngineeringEfficient MethodTmeda= NNatural SciencesDiversity-oriented SynthesisEfficient Palladium-catalyzed FormylationOrganic ChemistryLow PressureOrganometallic CatalysisCatalysisStereoselective SynthesisChemistryHeteroaryl BromidesAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
The key to the general and efficient palladium-catalyzed formylation of aryl and heteroaryl bromides is the use of the di-1-adamantyl-n-butylphosphane (cataCXium A) as ligand. Low pressure of the synthesis gas and appropriate choice of the base are also important for high yields (up to 99 %) of a broad range of (hetero)aromatic aldehydes at unprecedented low catalyst concentrations (see scheme; TMEDA= N,N,N′,N′-tetramethylethylenediamine).
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