Journal
ISRAEL JOURNAL OF CHEMISTRY
Volume -, Issue -, Pages -Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/ijch.202200051
Keywords
Carbenes; Gold; Catalysis; Asymmetric Catalysis; Nitrogen Heterocycles
Categories
Funding
- Centre National de la Recherche Scientifique (CNRS)
- Agence Nationale de la Recherche [ANR-21-CE07-0054-03]
- Agence Nationale de la Recherche (ANR) [ANR-21-CE07-0054] Funding Source: Agence Nationale de la Recherche (ANR)
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N-heterocyclic carbene (NHC) ligands have gained considerable importance in gold catalysis due to their appealing properties. Fused polyaromatic NHCs, featuring fused aromatic rings, have attracted wider attention in recent years for their unique structural and electronic properties. These versatile platforms offer superior activity and/or selectivity in NHC-gold catalysis and provide opportunities for further functionalization, chirality introduction, stimuli-responsiveness, or cooperativity within the NHC-gold systems.
Thanks to their appealing properties, N-heterocyclic carbene (NHC) ligands gained considerable significance as highly powerful ancillary ligands in gold catalysis. While NHC-gold catalysis is still dominated by the classical imidazole-derived NHC ligands, annelated NHC systems, which feature fused aromatic rings to the carbenic heterocycle, have drawn wider attention over the last few years thanks to their unique structural and electronic properties. Fused polyaromatic NHCs are indeed versatile platforms that offer unique stereoelectronic tuning possibilities to exhibit superior activity and/or selectivity in NHC-gold catalysis. But their polycyclic scaffolds also provide further scope for functionalization and the introduction of chirality, stimuli-responsiveness, or cooperativity within the NHC-gold systems. In this review, the recent advances in this area are discussed and a particular attention is drawn on the unique role of the annelation.
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