Palladium-catalyzed α-arylation of carbonyls in the de novo synthesis of aromatic heterocycles
Aromatic heterocycles are a very well represented motif in natural products and have found various applications in chemistry and material science, as well as being commonly found in pharmaceutical agents. Thus, new and efficient routes towards this class of compound are always desirable, particularl...
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Veröffentlicht in: | Organic & biomolecular chemistry 2015-04, Vol.13 (15), p.4367-4373 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | Aromatic heterocycles are a very well represented motif in natural products and have found various applications in chemistry and material science, as well as being commonly found in pharmaceutical agents. Thus, new and efficient routes towards this class of compound are always desirable, particularly if they expand the scope of chemical methodology or facilitate more effective pathways to complex substitution patterns. This perspective covers recent developments in the
de novo
synthesis of aromatic heterocycles
via
palladium-catalysed α-arylation reactions of carbonyls, which is itself a powerful transformation that has undergone significant development in recent years.
The enolate cross coupling reaction is a highly efficient method for the
de novo
synthesis of aromatic rings. |
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ISSN: | 1477-0520 1477-0539 |
DOI: | 10.1039/c5ob00055f |