Aminations of Aryl Bromides in Water at Room Temperature
- 14 August 2009
- journal article
- research article
- Published by Wiley in Advanced Synthesis & Catalysis
- Vol. 351 (11-12) , 1717-1721
- https://doi.org/10.1002/adsc.200900323
Abstract
Unsymmetrical di‐ and triarylamines can be formed under green chemistry conditions, taking advantage of micellar catalysis leading to palladium‐catalyzed aminations at ambient temperatures in water as the only medium.Keywords
This publication has 24 references indexed in Scilit:
- Evolution of a Fourth Generation Catalyst for the Amination and Thioetherification of Aryl HalidesAccounts of Chemical Research, 2008
- Biaryl Phosphane Ligands in Palladium‐Catalyzed AminationAngewandte Chemie International Edition in English, 2008
- Water-Mediated Catalyst Preactivation: An Efficient Protocol for C−N Cross-Coupling ReactionsOrganic Letters, 2008
- A New Class of Easily Activated Palladium Precatalysts for Facile C−N Cross-Coupling Reactions and the Low Temperature Oxidative Addition of Aryl ChloridesJournal of the American Chemical Society, 2008
- Highly Reactive, General and Long-Lived Catalysts for Palladium-Catalyzed Amination of Heteroaryl and Aryl Chlorides, Bromides, and Iodides: Scope and Structure–Activity RelationshipsJournal of the American Chemical Society, 2008
- A New Hybrid Phosphine Ligand for Palladium‐Catalyzed Amination of Aryl HalidesAdvanced Synthesis & Catalysis, 2008
- Room-Temperature Suzuki−Miyaura Couplings in Water Facilitated by Nonionic AmphiphilesOrganic Letters, 2008
- Reactions in Micellar SystemsAngewandte Chemie International Edition in English, 2005
- Expanding Pd-Catalyzed C−N Bond-Forming Processes: The First Amidation of Aryl Sulfonates, Aqueous Amination, and Complementarity with Cu-Catalyzed ReactionsJournal of the American Chemical Society, 2003
- Palladium-catalyzed amination of aromatic halides in water-containing solvent systems: a two-phase protocolChemical Communications, 1998