Abstract
The design and application of new homogeneous palladium catalysts for the formation of C-C and C-heteroatom bonds from aryl chloride substrates is reviewed. Much of the work performed in this area has focused on the synthesis of bulky, electron-rich phosphines and, more recently, carbenes that increase the electron density on the palladium centre(s) sufficiently to facilitate oxidative addition of the strong C-Cl bond. However, there has increasingly been an interest in the development of alternative palladium sources that improve activity when used in association with these ligands, for instance, palladacyclic complexes have played a particular role in this regard. (C) 2004 Elsevier B.V. All rights reserved.
Original language | English |
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Pages (from-to) | 2283-2321 |
Number of pages | 39 |
Journal | Coordination Chemistry Reviews |
Volume | 248 |
Issue number | 21-24 |
DOIs | |
Publication status | Published - Dec 2004 |
Keywords
- palladium
- catalyst
- heteroatom
- C-C bond forming
- coupling
- CROSS-COUPLING REACTIONS
- N-HETEROCYCLIC CARBENES
- HIGHLY-ACTIVE CATALYSTS
- HECK-TYPE REACTIONS
- ARYLBORONIC ACIDS
- ROOM-TEMPERATURE
- SUZUKI REACTION
- EFFICIENT CATALYSTS
- GENERAL-METHOD
- O BOND