13 research outputs found
Alumina and Silica Oxides as Catalysts for the Oxidation of Benzoins to Benzils under Solvent-free Conditions
Alumina or silica gel are used as catalysts for a solvent-free oxidation of benzoins to the corresponding benzils. These catalysts are easily recovered after completion of the reactions, which are carried out either by heating in a sand bath or using microwave irradiation. Comparison of the results obtained with both catalysts indicates that all the reactants examined were oxidized faster on alumina than on silica under these conditions
Alumina and Silica Oxides as Catalysts for the Oxidation of Benzoins to Benzils under Solvent-free Conditions
Abstract: Alumina or silica gel are used as catalysts for a solvent-free oxidation of benzoins to the corresponding benzils. These catalysts are easily recovered after completion of the reactions, which are carried out either by heating in a sand bath or using microwave irradiation. Comparison of the results obtained with both catalysts indicates that all the reactants examined were oxidized faster on alumina than on silica under these conditions
New synthetic protocol for stereoselective synthesis of diethyl 1,2-dicyano-3-alkyl-(aryl)cyclopropane-1,2-dicarboxylate
Synthesis, spectroscopic and photophysical studies of xanthene derivatives
We report on the experimental, crystal structure and computational investigation of a new class of xanthenes obtained by the reaction of salicylaldehyde and its derivatives with, 5,5-Dimethylcyclohexane-1,3-dione (Dimedone). The synthesized xanthenes were characterized by state-of-the-art techniques, such as IR, Raman, 1H and 13C NMR, Single Crystal X-ray crystallography, UV–Vis and photophysical measurements. The structure, ground- and excited-state properties of one xanthene derivative was investigated using Density Functional Theory (DFT) and Time-Dependent DFT (TD-DFT) calculations with and without solvent (ethanol). The optimized geometries and predicted IR frequencies were in good agreement with experimental data. Hirshfeld surface analyses were carried out to gain insight on the close-contact interactions of the crystal, where hydrogen showed the highest contribution (66.1%). The synthetic route proposed in this work does not use any catalysts and leads to high yields (75–85%), therefore being an interesting alternative to synthesize xanthene derivatives. © 2017 Elsevier B.V
Investigation of interactional behavior and relative photo-physical properties in a group of bioactive compounds
In recent years, numerous researchers have faced the challenge of synthesizing bioactive compounds. Hence, chalcones with bioactive anti�cancer characteristics have attracted interests in many pharmaceutical studies. In this work, we focused on photo�physical behavior of three chalcones, with similar structures, in various solvent media, in order to study and compare their similarities and differences. Theoretical techniques were used to validate the experimental results. The experimental and theoretical results help to expand and better the realization of the photo�physical characteristics of these compounds and reveal essential information about the activity of this group of compounds in biological systems. The results show that photo�physical behavior of the chalcones is related to the solvent�solute interactions. Linear solvation energy relationship (LSER)model of Kamlet�Abboud�Taft and Catalán were used to analyze the interactions of chalcones in various media. The ground and excited state dipole moments of these bioactive compounds were obtained using Lippert's, Bakshiev's and Ghamma�Viallet's solvatochromic shift methods and their molecular resonance forms were presented. Finally, these results were compared and discussed by time�dependent density functional theory and configuration interaction calculations. © 2019 Elsevier B.V
The organocatalytic role of L-(+)-tartaric acid in the synthesis of 5-aryl-1,1′- and 5-aryl-3,1′-dimethyl-1H,1′H-spiro[furo[2,3-d]pyrimidine-6,5′-pyrimidine]2,2′,4,4′,6′(3H,3′H,5H)-pentaones
Alumina and Silica Oxides as Catalysts for the Oxidation of Benzoins to Benzils under Solvent-free Conditions
Alumina or silica gel are used as catalysts for a solvent-free oxidation of benzoins to the corresponding benzils. These catalysts are easily recovered after completion of the reactions, which are carried out either by heating in a sand bath or using microwave irradiation. Comparison of the results obtained with both catalysts indicates that all the reactants examined were oxidized faster on alumina than on silica under these conditions