RSC Advances · 2013 · 37 citations · 23 references
Schiff BaseChemical EngineeringAromatic AldehydesEngineeringHeterogeneous CatalysisSustainable SynthesisOrganic ChemistryCatalysisExcellent RecyclabilityChemistryMolecular CatalysisAsymmetric CatalysisMcm-41/schiff BaseEnantioselective SynthesisCatalytic Synthesis
By employing a MCM-41/Schiff base as catalyst, high yield Knoevenagel condensation reactions of malononitrile with aromatic aldehydes were realized. The reaction afforded the corresponding products in excellent yields (up to 99%) in water. Moreover, the catalyst was also found to exhibit excellent recyclability (up to 10 times) without loss of efficiency.
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Trienamines in Asymmetric Organocatalysis: Diels−Alder and Tandem Reactions
Zhi‐Jun Jia, Hao Jiang, Jun‐Long Li et al. · Journal of the American Chemical Society · 2011 · 389 citations
Gen Zhang, Yaohu Zhang, Jiexi Yan et al. · The Journal of Organic Chemistry · 2011 · 210 citations
Combinatorial Chemistry, Bioorganic Chemistry, Organic Chemistry +20