4.4 Article

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

Journal

CHEMISTRYSELECT
Volume 6, Issue 6, Pages 1238-1243

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/slct.202004158

Keywords

Bifunctionalization; Cross-Coupling; Domino Reaction; Knoevenagel Condensation; Magnetic Nanoparticles

Funding

  1. Natural Science Foundation of Jiangsu Province of China [BK2010485]
  2. Qing Lan Project of Jiangsu Province, P. R. China

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The novel magnetic nanoparticle-supported bifunctional catalyst NH-Pd(0)@MNP was successfully prepared and evaluated in a one-pot tandem reaction, producing a series of biaryl derivatives under phosphine-free conditions. The catalyst can be easily separated using an external magnetic field and reused multiple times without significant loss of catalytic activity.
A novel magnetic nanoparticle-supported bifunctional catalyst NH-Pd(0)@MNP was prepared and its activity was evaluated in one-pot Suzuki coupling-Knoevenagel condensation tandem reaction. A series of biaryl derivatives were synthesized via sequential Suzuki coupling-Knoevenagel condensation in ethanol/water medium under phosphine-free conditions. Meanwhile, the catalyst could be easily separated by an external magnetic field, and could be reused several times without remarkable loss of catalytic activity.

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