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
Hauptverfasser: Liu, Jin, Jin, Shaofen, Zhou, Yingxing, Ni, Dongmei, Liu, Tingting, Cui, Bingcun, Hu, Gang, Yu, Xin, Huang, Guosheng
Format: Artikel
Sprache:eng
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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.
ISSN:0039-7881
1437-210X
DOI:10.1055/s-0039-1691564