16 results on '"Eddahmi, Mohammed"'
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2. Structure-property relationship of N-substituted triazolonitroindazoles: A comprehensive study on linear and non-linear optics, as a function of quantum parameters employing density function theory
3. Towards Alzheimer’s disease-related targets: One-pot Cu(I)- mediated synthesis of new nitroindazolyltriazoles
4. Anticorrosion Properties of Indazole Derivative for Corrosion Inhibition of Carbon Steel in 1 M HCl
5. Synthesis, Molecular Electron Density Theory Study, Molecular Docking, and Pharmacological Evaluation of New Coumarin–Sulfonamide–Nitroindazolyl–Triazole Hybrids as Monoamine Oxidase Inhibitors.
6. An insight into the vicarious nucleophilic substitution reaction of 2-nitro-5,10,15,20-tetraphenylporphyrin with p-chlorophenoxyacetonitrile: Synthesis and gas-phase fragmentation studies
7. Theoretical study of the stability and reactivity of nitro-coumarins and amino-coumarins by DFT method
8. Study of N‐methyl‐5‐nitroindazolylacrylonitriles as a Function of Quantum Parameters Employing Density Function Theory Methods: Comparative Theoretical Study and Nonlinear Optical Properties
9. Synthesis and Biological Properties of Coumarin Derivatives. A Review
10. Antiproliferative and apoptotic activity of new indazole derivatives as potential anticancer agents
11. New nitroindazole-porphyrin conjugates: Synthesis, characterization and antibacterial properties
12. A Suitable Functionalization of Nitroindazoles with Triazolyl and Pyrazolyl Moieties via Cycloaddition Reactions
13. Synthesis and Biological Evaluation of New Functionalized Nitroindazolylacetonitrile Derivatives
14. New nitroindazolylacetonitriles: efficient synthetic accessviavicarious nucleophilic substitution and tautomeric switching mediated by anions
15. New nitroindazolylacetonitriles: efficient synthetic access via vicarious nucleophilic substitution and tautomeric switching mediated by anions.
16. A Suitable Functionalization of Nitroindazoles with Triazolyl and Pyrazolyl Moieties via Cycloaddition Reactions.
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