An N‐Heterocyclic Carbene Ligand with Flexible Steric Bulk Allows Suzuki Cross‐Coupling of Sterically Hindered Aryl Chlorides at Room Temperature
- 7 August 2003
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 42 (31), 3690-3693
- https://doi.org/10.1002/anie.200351325
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Macromolecular Effect: Synthesis of a Ferrocenylmethylphosphine-Containing Polymer as Highly Efficient Ligands for Room-Temperature Palladium(0)-Catalyzed Suzuki Cross-Coupling Reactions of Aryl ChloridesJournal of the American Chemical Society, 2003
- Unparalleled Rates for the Activation of Aryl Chlorides and Bromides: Coupling with Amines and Boronic Acids in Minutes at Room TemperatureAngewandte Chemie, 2002
- Palladium-Catalyzed Coupling Reactions of Aryl ChloridesAngewandte Chemie International Edition, 2002
- Simple Mixed Tricyclohexylphosphane–Triarylphosphite Complexes as Extremely High-Activity Catalysts for the Suzuki Coupling of Aryl ChloridesAngewandte Chemie International Edition, 2002
- Suzuki−Miyaura Cross-Coupling Reactions Mediated by Palladium/Imidazolium Salt SystemsOrganometallics, 2002
- A Highly Active Suzuki Catalyst for the Synthesis of Sterically Hindered Biaryls: Novel Ligand CoordinationJournal of the American Chemical Society, 2002
- Stable CarbenesChemical Reviews, 1999
- Palladium−Imidazol-2-ylidene Complexes as Catalysts for Facile and Efficient Suzuki Cross-Coupling Reactions of Aryl Chlorides with Arylboronic AcidsThe Journal of Organic Chemistry, 1999
- Auf der Suche nach Stabilen CarbenenChemie in Unserer Zeit, 1998
- Palladium-Catalyzed Cross-Coupling Reactions of Organoboron CompoundsChemical Reviews, 1995