Abstract
β-amide ketones were synthesised by a three-component one-pot reaction of phenylacetylene, aldehydes, and amides in anhydrous acetonitrile containing trifluoroacetic acid and acetic acid in the presence of AlCl3 catalyst. The title compound structures were identified by 1H NMR, 13C NMR, MS, and elemental analysis.
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© 2013 Institute of Chemistry, Slovak Academy of Sciences
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Artikel in diesem Heft
- Application of umbelliferone molecularly imprinted polymer in analysis of plant samples
- Determination of antioxidant activity using oxidative damage to plasmid DNA — pursuit of solvent optimization
- Nanosized sulfated zirconia as solid acid catalyst for the synthesis of 2-substituted benzimidazoles
- Removal of heavy metal ions from aqueous solutions using low-cost sorbents obtained from ash
- Base-catalysed reduction of pyruvic acid in near-critical water
- Solubility and micronisation of phenacetin in supercritical carbon dioxide
- Synthesis of nanostructured perovskite powders via simple carbonate co-precipitation
- Three-component one-pot reaction for the synthesis of β-amide ketones
- Spectral analysis of naringenin deprotonation in aqueous ethanol solutions
- Provenance study of volcanic glass using 266–1064 nm orthogonal double pulse laser induced breakdown spectroscopy
- A new, fully validated and interpreted quantitative structure-activity relationship model of p-aminosalicylic acid derivatives as neuraminidase inhibitors
- Interaction of oligonucleotides with benzo[c]phenanthridine alkaloid sanguilutine