Highly Active, Air-Stable Versatile Palladium Catalysts for the C−C, C−N, and C−S Bond Formations via Cross-Coupling Reactions of Aryl Chlorides

This publication has 10 references indexed in Scilit:

• A Novel and Highly Stereoselective Intramolecular Formal [3+3] Cycloaddition Reaction of Vinylogous Amides Tethered withα,β-Unsaturated Aldehydes: A Formal Total Synthesis of (+)-Gephyrotoxin
  Angewandte Chemie International Edition in English, 2001
• Enantioselective Reduction of Ketones Catalyzed by Polymer-Supported Sulfonamide Using NaBH4/Me3SiCl (or BF3⋅OEt2) as Reducing Agent
  Angewandte Chemie International Edition in English, 2001
• Screening of Homogeneous Catalysts by Fluorescence Resonance Energy Transfer. Identification of Catalysts for Room-Temperature Heck Reactions
  Journal of the American Chemical Society, 2001
• Synthesis of 2,3-Dihydroindoles, Indoles, and Anilines by Transition Metal-Free Amination of Aryl Chlorides
  The Journal of Organic Chemistry, 2001
• Aromatic Aminations by Heterogeneous Ni0/C Catalysis
  Angewandte Chemie International Edition in English, 2000
• Alkyl- and Arylthiodediazoniations of Dry Arenediazoniumo-Benzenedisulfonimides. Efficient and Safe Modifications of the Stadler and Ziegler Reactions to Prepare Alkyl Aryl and Diaryl Sulfides
  The Journal of Organic Chemistry, 2000
• The First General Method for Stille Cross-Couplings of Aryl Chlorides
  Angewandte Chemie International Edition in English, 1999
• Palladacycles: Efficient New Catalysts for the Heck Vinylation of Aryl Halides
  Chemistry – A European Journal, 1997
• Transformations of Chloroarenes, Catalyzed by Transition-Metal Complexes
  Chemical Reviews, 1994
• Evidence of the formation of zerovalent palladium from Pd(OAc)2 and triphenylphosphine
  Organometallics, 1992