Synthetic Approaches to Sterically Hindered N‐Arylimidazoles through Copper‐Catalyzed Coupling Reactions
- 1 April 2005
- journal article
- research article
- Published by Wiley in European Journal of Organic Chemistry
- Vol. 2005 (8) , 1637-1643
- https://doi.org/10.1002/ejoc.200400453
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Highly Efficient and Mild Copper‐Catalyzed N‐ and C‐Arylations with Aryl Bromides and IodidesChemistry – A European Journal, 2004
- Copper−Diamine-Catalyzed N-Arylation of Pyrroles, Pyrazoles, Indazoles, Imidazoles, and TriazolesThe Journal of Organic Chemistry, 2004
- Mild Conditions for Copper‐Catalysed N‐Arylation of PyrazolesEuropean Journal of Organic Chemistry, 2004
- Synthesis of Secondary Arylamines through Copper-Mediated Intermolecular Aryl AminationOrganic Letters, 2003
- A simple copper salt catalysed the coupling of imidazole with arylboronic acids in protic solventDedicated to Professor Xie Ming-Gui on the occasion of his 65th birthday.Chemical Communications, 2003
- Modern Synthetic Methods for Copper‐Mediated C(aryl)-O, C(aryl)-N, and C(aryl)-S Bond FormationAngewandte Chemie International Edition in English, 2003
- Potassium Trifluoro(organo)borates: New Perspectives in Organic ChemistryEuropean Journal of Organic Chemistry, 2003
- Chiral N-heterocyclic carbene-transition metal complexes in asymmetric catalysisTetrahedron: Asymmetry, 2003
- Optically Active Iridium Imidazol-2-ylidene-oxazoline Complexes: Preparation and Use in Asymmetric Hydrogenation of ArylalkenesJournal of the American Chemical Society, 2002
- Open-Chain Dications and Betaines with Imidazolium Molecular Motifs: Synthesis and Structural AspectsEuropean Journal of Organic Chemistry, 2002