Palladium-Catalyzed ortho-Monoacylation of Arenes with Aldehydes via 1,2,4-Benzotriazine-Directed C–H Bond Activation
Abstract An efficient palladium-catalyzed C–H bond functionalization/ ortho -monoacylation reaction of 3-aryl-1,2,4-benzotriazines with (hetero)aryl or alkyl aldehydes has been developed, which offers a facile and alternative strategy for direct modification and further diversification of 3-aryl-1,2...
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Veröffentlicht in: | Synthesis (Stuttgart) 2020-05, Vol.52 (9), p.1407-1416 |
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Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | Abstract
An efficient palladium-catalyzed C–H bond functionalization/
ortho
-monoacylation reaction of 3-aryl-1,2,4-benzotriazines with (hetero)aryl or alkyl aldehydes has been developed, which offers a facile and alternative strategy for direct modification and further diversification of 3-aryl-1,2,4-benzotriazines. Bioactive 1,2,4-benzotriazine has been employed as a novel directing group for the palladium-catalyzed regioselective monoacylation of sp
2
C–H bond protocol with broad substrate scope and good functional group tolerance. |
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ISSN: | 0039-7881 1437-210X |
DOI: | 10.1055/s-0039-1691564 |