One‐pot Suzuki Coupling‐Knoevenagel Condensation Tandem Reaction Catalyzed by a Recyclable Magnetic Bifunctional Catalyst

Yuan, Xiaofeng; Wang, Jin‐Yuan; Wan, Zijuan; Zhang, Qiang; Luo, Jun

doi:10.1002/slct.202004158

Cited by 4 publications

(2 citation statements)

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“… 12 , 13 Also, composites containing metal oxides showed high reactivity as heterogeneous catalysts for Knoevenagel condensation, and the metal oxides in these composites were prior chemically modified or doped with metals. 14 − 17 …”

Section: Introductionmentioning

confidence: 99%

“…Because of these limitations, many efforts have been devoted in this area to find alternative routes to perform this reaction under base-free conditions. Previous studies have reported the use of different heterogeneous catalysts containing zeolites, mesoporous silica, ionic liquids, and graphitic carbon nitride. , Also, composites containing metal oxides showed high reactivity as heterogeneous catalysts for Knoevenagel condensation, and the metal oxides in these composites were prior chemically modified or doped with metals. − …”

Section: Introductionmentioning

confidence: 99%

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Ag@TiO₂ Nanocomposite as an Efficient Catalyst for Knoevenagel Condensation

et al. 2022

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In the present study, a new series of different heterocycles was synthesized through base-free Knoevenagel condensation of various aldehydes and active methylene-containing compounds using the hydrothermal developed Ag@TiO 2 as a heterogeneous catalyst. The catalyst was synthesized by mixing TiO 2 (P25) with AgNO 3 and hydrothermally treated in ethanol at 180 °C for 12 h. The developed Ag@TiO 2 catalyst was directly applied for Knoevenagel condensation, and the optimized procedure involved stirring the aldehydes and active methylene-containing compounds with Ag@TiO 2 in ethanol at 65 °C. The reaction scope was investigated for various aromatic and heterocyclic aldehydes with active methylene-containing compounds, and the isolated yields were significantly high. The reusability of the catalyst was investigated for up to five cycles, where an insignificant decrease in the catalyst’s reactivity was observed. Also, the reaction could proceed in water as a solvent, and the isolated yield was 40%. Hence, this protocol features mild reaction conditions, a facile procedure, and clean reaction profiles.

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