Suzuki–Miyaura cross-coupling of aryl and alkyl halides using palladium/imidazolium salt protocols
- 19 April 2004
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 45 (17) , 3511-3515
- https://doi.org/10.1016/j.tetlet.2004.02.134
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- The First Applications of Carbene Ligands in Cross-Couplings of Alkyl Electrophiles: Sonogashira Reactions of Unactivated Alkyl Bromides and IodidesJournal of the American Chemical Society, 2003
- Transition‐Metal‐Free Suzuki‐Type Coupling ReactionsAngewandte Chemie International Edition in English, 2003
- Palladium-Catalyzed Coupling Reactions of Aryl ChloridesAngewandte Chemie International Edition in English, 2002
- Suzuki−Miyaura Cross-Coupling Reactions Mediated by Palladium/Imidazolium Salt SystemsOrganometallics, 2002
- Room-Temperature Alkyl−Alkyl Suzuki Cross-Coupling of Alkyl Bromides that Possess β HydrogensJournal of the American Chemical Society, 2001
- Versatile Catalysts for the Suzuki Cross-Coupling of Arylboronic Acids with Aryl and Vinyl Halides and Triflates under Mild ConditionsJournal of the American Chemical Society, 2000
- Highly Active Palladium Catalysts for Suzuki Coupling ReactionsJournal of the American Chemical Society, 1999
- Metal Vapor Synthesis as a Straightforward Route to Group 10 Homoleptic Carbene ComplexesOrganometallics, 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
- Palladium-Catalyzed Cross-Coupling Reactions of Organoboron CompoundsChemical Reviews, 1995