Formation of bicyclic pyrroles from the catalytic coupling reaction of 2,5-disubstituted pyrroles with terminal alkynes, involving the activation of multiple C–H bonds()

Míreanna Comhchosúla

• Regioselective Formation of α-Vinylpyrroles from the Ruthenium-Catalyzed Coupling Reaction of Pyrroles and Terminal Alkynes Involving C–H Bond Activation
  le: Gao, Ruili, et al.
  Foilsithe: (2010)
• Scope and Mechanistic Investigations on the Solvent-Controlled Regio- and Stereoselective Formation of Enol Esters from the Ruthenium-Catalyzed Coupling Reaction of Terminal Alkynes and Carboxylic Acids
  le: Yi, Chae S., et al.
  Foilsithe: (2009)
• Scope and Mechanistic Study of the Ruthenium-Catalyzed Ortho-C-H Bond Activation and Cyclization Reactions of Arylamines with Terminal Alkynes
  le: Yi, Chae S., et al.
  Foilsithe: (2005)
• Synthesis of N-perfluoroalkyl-3,4-disubstituted pyrroles by rhodium-catalyzed transannulation of N-fluoroalkyl-1,2,3-triazoles with terminal alkynes
  le: Bakhanovich, Olga, et al.
  Foilsithe: (2021)
• Terminal Alkyne Coupling Reactions through a Ring: Mechanistic Insights and Regiochemical Switching
  le: Storey, Caroline M., et al.
  Foilsithe: (2018)