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A Copper(<scp>II</scp>)‐Catalyzed Aza‐Friedel–Crafts Reaction of <i>N</i>‐(2‐Pyridyl)sulfonyl Aldimines: Synthesis of Unsymmetrical Diaryl Amines and Triaryl Methanes
232
Citations
55
References
2005
Year
Aza‐friedel–crafts ReactionElectron-rich ArenesEngineeringOrganic ChemistryChemistrySulfonyl MoietyChemical EngineeringOrganometallic CatalysisCatalyst SystemCross-coupling ReactionDiversity-oriented SynthesisCatalysisSulfonyl AldiminesTriaryl MethanesAsymmetric CatalysisCatalytic SynthesisNatural SciencesMolecular CatalysisSynthetic Chemistry
The choice of the (2-pyridyl)sulfonyl moiety as an N-protecting group and Cu(OTf)2/(±)-binap as catalyst system lead to a highly efficient aza-Friedel–Crafts reaction of electron-rich arenes (Ar2-H) and heteroarenes with N-sulfonyl imines. This protocol is also amenable to the synthesis of unsymmetrical triaryl methanes through a second electrophilic aromatic substitution with a different electron-rich arene (Ar3-H; see scheme).
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