Skip to content

The Buchwald Research Group

Menu

  • Research
  • Publications
  • Stephen Buchwald
  • Team
  • News
  • Contact
  • Login

Archives

A General and Efficient Copper Catalyst for the Amidation of Aryl Halides

A General, Efficient, and Inexpensive Catalyst System for the Coupling of Aryl Iodides and Thiols

Copper-Catalyzed Coupling of Alkylamines and Aryl Iodides:  An Efficient System Even in an Air Atmosphere

An Annulative Approach to Highly Substituted Indoles:  Unusual Effect of Phenolic Additives on the Success of the Arylation of Ketone Enolates

One-Pot Synthesis of Unsymmetrical Triarylamines from Aniline Precursors

Pd(PhCN)2Cl2/P(t-Bu)3:  A Versatile Catalyst for Sonogashira Reactions of Aryl Bromides at Room Temperature

Synthesis of β-Alkyl Cyclopentanones in High Enantiomeric Excess via Copper-Catalyzed Asymmetric Conjugate Reduction

Efficient Palladium-CatalyzedN-Arylation of Indoles

An Improved Synthesis of Functionalized Biphenyl-Based Phosphine Ligands

A High-Yield, General Method for the Catalytic Formation of Oxygen Heterocycles

  • ← Previous
  • Next →
Copyright © 2025 The Buchwald Research Group. All rights reserved.
Theme: Accelerate by ThemeGrill. Powered by WordPress.
  • Research
  • Publications
  • Stephen Buchwald
  • Team
  • News
  • Contact
  • Login