Planar-Chiral [2.2]Paracyclophane-Based Amides as Proligands for Titanium- and Zirconium-Catalyzed Hydroamination
A synthetic route to racemic and enantiopure planar chiral [2.2]paracyclophanes with amide groups was developed to combine the well-established reactivity of amides as N,O-chelating ligands in hydroamination reactions with the planar chirality of the [2.2
Molecular Complexes of Cyclophanes, XVIII: Spectroscopic and Thermodynamic Studies on the Charge-Transfer Complexes Between 4-(Paracyclophanoyl)amines and ?-Acceptors
The charge-transfer (CT) complexes of several substituted 4-(paracyclophanoyl)amines as donors with tetracyanoethylene (TCNE) and 2,3-dichloro-5,6-dicyanobenzoquinone (DDQ) as ?-acceptors have been studied spectrophotometrically.The role of the molec