textjournal article
N-Heterocyclic Pyridylmethylamines: Synthesis, Complexation, Molecular Structure, and Application to Asymmetric Suzuki–Miyaura and Oxidative Coupling Reactions
Abstract
The synthesis of N,N-bidentate ligands based on a π-deficient N-heterocyclic pyridylmethylamine core is described. The preparation and characterization of the corresponding N,N-ligand–palladium complexes in solution and the solid state are illustrated. Pd complexes showed a good yield and moderate catalytic activity (up to 40% ee) in the asymmetric Suzuki–Miyaura coupling reaction, leading to methoxybinaphthyl derivatives. The combination of N,N-pyridylmethylamines with cuprous iodide revealed effective catalytic systems in oxidative naphthol derivative coupling reactions, affording the corresponding binaphthyls in high yields and with enantioselectivities of up to 61%- Text
- Journal contribution
- Biochemistry
- Medicine
- Biotechnology
- Sociology
- Chemical Sciences not elsewhere classified
- characterization
- ee
- solution
- Application
- Pyridylmethylamine
- Suzuki
- ligand
- Asymmetric
- Complexation
- Oxidative
- oxidative naphthol
- core
- combination
- Molecular Structure
- enantioselectivitie
- pyridylmethylamine
- yield
- preparation
- methoxybinaphthyl derivatives
- ReactionsThe synthesis
- Pd complexes
- cuprous iodide
- Synthesi