Cu-Catalyzed three-component coupling reactions using nitriles, 1,3-dienes and silylboranes

This paper reports novel Cu-catalyzed three-component coupling reactions using nitriles, 1,3-dienes and silylboranes. The desired reactions proceed at room temperature and yield β,γ-unsaturated ketones with a (dimethylphenylsilyl)methyl moiety at the α-position. Diverse nitriles participate in the r...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2020-04, Vol.56 (34), p.4648-4651
Hauptverfasser: Matsuda, Yuki, Tsuji, Yasushi, Fujihara, Tetsuaki
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Sprache:eng
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Zusammenfassung:This paper reports novel Cu-catalyzed three-component coupling reactions using nitriles, 1,3-dienes and silylboranes. The desired reactions proceed at room temperature and yield β,γ-unsaturated ketones with a (dimethylphenylsilyl)methyl moiety at the α-position. Diverse nitriles participate in the reaction and the corresponding products were obtained in good to high yields with high regioselectivity. Novel Cu-catalyzed three-component coupling reactions using nitriles, 1,3-dienes and silylboranes have been achieved. The desired reactions proceed at room temperature and yield β,γ-unsaturated ketones.
ISSN:1359-7345
1364-548X
DOI:10.1039/d0cc01803a