• Title/Summary/Keyword: Environmentally Eco-friendly Benign Reaction

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ZrOCl2.8H2O as an Efficient Catalyst for the Three-Component Synthesis of Triazoloindazoles and Indazolophthalazines

  • Tavakoli, Hamid Reza;Moosavi, Sayed Mojtaba;Bazgir, Ayoob
    • Journal of the Korean Chemical Society
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    • v.57 no.4
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    • pp.472-475
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    • 2013
  • An efficient and environmentally benign protocol for the three-component synthesis of triazoloindazoles and indazolophthalazines via condensation of dimedone, aldehydes and urazole or phthalhydrazide catalyzed by $ZrOCl_2.8H_2O$ as an inexpensive and eco-friendly catalyst with high catalytic activity under solvent-free conditions is reported. This protocol provides a new and improved method for obtaining triazoloindazoles and indazolophthalazines in terms of good yields, simple experimental procedure and short reaction time.

ZrOCl2·8H2O as an Efficient Catalyst for the Pseudo Four-Component Synthesis of Benzopyranopyrimidines

  • Tavakoli, Hamid Reza;Moosavi, Sayed Mojtaba;Bazgir, Ayoob
    • Journal of the Korean Chemical Society
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    • v.57 no.2
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    • pp.260-263
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    • 2013
  • An efficient and environmentally benign protocol for the pseudo four-component synthesis of benzopyranopyrimidines via condensation of salicylic aldehydes, malononitrile and various amines catalyzed by $ZrOCl_2{\cdot}8H_2O$ as an inexpensive and eco-friendly catalyst with high catalytic activity under solvent-free conditions is reported. This protocol provides a new and improved method for obtaining benzopyranopyrimidines in terms of good yields, simple experimental procedure and short reaction time.

Synthesis, Characterization and Correlation Analysis in Styryl 6-Methoxy-2-Naphthyl Ketones (Styryl-6-Methoxy-2-Naphthyl Ketone 유도체의 합성 및 특성 분석)

  • Thirunarayanan, G.
    • Journal of the Korean Chemical Society
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    • v.51 no.2
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    • pp.115-124
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    • 2007
  • A series of α, β-unsaturated ketones are synthesized by Crossed - Aldol condensation reaction, from ecofriendly 6-methoxy-2-naphthyl ketones and substituted benzaldehydes under solvent free conditions using silica-sulfuric acid as a catalytic reagent. The yields of ketones are more than 90% and the catalyst was reusable for further run. There is no appreciable decrease in the yield of product and the activity of catalyst. These chalcones were characterized by their physical constants and spectral data (IR, 1H-, 13C-NMR and Mass). These spectral data are subjected to correlate various Hammett substituent constants with single and multiparameter correlation equations. From the results of statistical analysis the influence of electronic effects of substituents on the spectral data of the ketones were explained.