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Water Promoted One Pot Synthesis of Sesamol Derivatives as Potent Antioxidants: DFT, Molecular Docking, SAR and Single Crystal Studies

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dc.contributor.author Lalpara, J. N.
dc.contributor.author Hadiyal, S. D.
dc.contributor.author Dhaduk, B. B.
dc.contributor.author Gupta, M. K.
dc.contributor.author Solanki, M. B.
dc.contributor.author Sharon, A.
dc.contributor.author Dubal, G. G.
dc.date.accessioned 2024-11-19T05:24:39Z
dc.date.available 2024-11-19T05:24:39Z
dc.date.issued 2023
dc.identifier.citation Lalpara, J. N., Hadiyal, S. D., Dhaduk, B. B., Gupta, M. K., Solanki, M. B., Sharon, A., & Dubal, G. G. (2023). Water promoted one pot synthesis of sesamol derivatives as potent antioxidants: DFT, molecular docking, SAR and single crystal studies. Polycyclic Aromatic Compounds, 43(5), 4070-4083. en_US
dc.identifier.uri http://10.9.150.37:8080/dspace//handle/atmiyauni/1665
dc.description.abstract A one pot water mediated synthesis of sesamol analogous using Betti Base synthetic approach. The reaction was optimized with various solvents and catalysts, but the product formed with a high yield in aqueous ethanol condition. The examined strategy offers many advantages such as green solvent, purification without column chromatography, and catalyst-free synthesis. The synthesized molecules were investigated for molecular docking and DFT studies. In silico parameter showed that the compound 4h has the lowest affinity score as well as high charge transformations. From the result of theoretical approaches, we evaluate compounds for in vitro antioxidant assay toward the DPPH, H2O2 and NO method with 50 µg/mL concentration. In vitro bioassay revealed that the compound 4 h had excellent inhibition capacity. en_US
dc.language.iso en en_US
dc.publisher Polycyclic Aromatic Compounds en_US
dc.subject Antioxidant; Betti base en_US
dc.subject DFT en_US
dc.subject molecular docking en_US
dc.subject Sesamol derivatives en_US
dc.title Water Promoted One Pot Synthesis of Sesamol Derivatives as Potent Antioxidants: DFT, Molecular Docking, SAR and Single Crystal Studies en_US
dc.type Article en_US


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