Carbon−Carbon Bond Formation through Double sp2 C−H Activations: Synthesis of Ferrocenyl Oxazoline Derivatives
Organometallics2007Vol. 26(20), pp. 4869–4871
Citations Over TimeTop 1% of 2007 papers
Abstract
Direct arylation of simple arenes with ferrocenyl oxazolines was achieved in the presence of a stoichiometric amount of Pd(OAc)2 or a catalytic amount of palladium with excess oxidant such as Cu(OAc)2. This double sp2 C−H activation process provides a unique access to the aryl-substituted ferrocene derivatives, even in the enantiopure form of planar chirality, in a few steps from readily available starting materials.
Related Papers
- → Synthesis of Enantiopure γ‐Lactones via a RuPHOX‐Ru Catalyzed Asymmetric Hydrogenation of γ‐Keto Acids(2018)26 cited
- → Synthesis of Enantiopure 5-Substituted 2,3-Methanopyrrolidines by Cyclization of Enantiopure α-Branched α-N-Homoallylamino Nitriles(2012)8 cited
- → A Valuable Synthetic Route to the Enantiopure Functionalized N‐Substituted Aziridines(2004)1 cited
- → ChemInform Abstract: Efficacious and Rapid Metal‐ and Solvent‐Free Synthesis of Enantiopure Oxazolines.(2015)
- → ChemInform Abstract: Chiral Pyridin‐3‐ones and Pyridines: Syntheses of Enantiopure 2,4‐Disubstituted 6‐Hydroxy‐1,6‐dihydro‐2H‐pyridin‐3‐ones, 2,3‐Disubstituted 4‐Iodopyridines, and Enantiopure 2,3‐Disubstituted 4‐Pyridinemethanols.(2012)