Allylic Amination andN-Arylation-Based Domino Reactions Providing Rapid Three-Component Strategies to Fused Pyrroles with Different Substituted Patterns

Citations Over TimeTop 10% of 2012 papers

Abstract

New three-component domino reaction providing divergent approaches to multifunctionalized fused pyrroles with different substituted patterns have been established (40 examples). The direct C(sp(3))-N bond formation was achieved through intermolecular allylic amination in a one-pot operation, and N-arylation of amines was realized by varying N-amino acid enaminones. The reaction is easy to perform simply by mixing three common reactants in acetic acid under microwave heating. The reaction proceeds at fast rates and can be finished within 30 min, which makes workup convenient to give good chemical yields.

Related Papers

• → Palladium‐Catalyzed Branch‐ and Z‐Selective Allylic C−H Amination with Aromatic Amines(2022)30 cited
• → Palladium‐Catalyzed Branch‐ and Z‐Selective Allylic C−H Amination with Aromatic Amines(2022)4 cited
• → ChemInform Abstract: Synthesis of Monofluoroalkenes via the Activation of Allylic C—F Bonds: A Novel Route to β‐Aminofluoroalkenes Using Pd‐Catalyzed Allylic Amination Reactions of 3,3‐Difluoropropenes(2011)
• → Asymmetric Copper-Catalyzed Allylic Amination and Oxidation Reactions(2005)
• → Ir-Catalyzed Allylic Amination and Etherification(2005)