Thoraya Farghaly
Professor of Chemistry
Cairo University, Giza, Egypt
(email)
Khan, I., W. Rehman, F. Rahim, R. Hussain, S. Khan, S. Fazil, L. Rasheed, M. Taha, S. A. A. Shah, M. H. Abdellattif, et al.,
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Synthesis, In Vitro α-Glucosidase Inhibitory Activity and Molecular Docking Study of New Benzotriazole-Based Bis-Schiff Base Derivatives
",
Pharmaceuticals
, vol. 16, pp. 17, 2023.
Al-Soliemy, A. M., T. A. Farghaly, E. M. H. Abbas, M. R. Shaaban, M. E. M. Zayed, and T. B. A. Al-Naggar,
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Synthesis of thiazolyl-N-phenylmorepholine derivatives and their biological activities
",
Medicinal Chemistry
, vol. 17, pp. 790-805, 2021.
Alnaja, A. A. M., T. A. Farghaly, H. S. A. El-Zahabi, and M. R. Shaaban,
"
Cytotoxicity, Docking Study of New Fluorinated Fused Pyrimidine Scaffold: Thermal and Microwave Irradiation Synthesis
",
Medicinal Chemistry
, vol. 17, pp. 501-518, 2021.
Khalil, K. D., S. M. Riyadh, M. Jaremko, T. A. Farghaly, and M. Hagar,
"
Synthesis of Chitosan-La2O3 Nanocomposite and Its Utility as a Powerful Catalyst in the Synthesis of Pyridines and Pyrazoles
",
Molecules
, vol. 26, pp. 3689, 2021.
Mahmoud, H. K., S. M. Gomha, T. A. Farghaly, and H. M. Awad,
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Synthesis of Thiazole Linked Imidazo[2,1-b]Thiazoles as Anticancer Agents
",
POLYCYCLIC AROMATIC COMPOUNDS
, vol. 41, pp. 1608–1622, 2021.
Farghaly, T. A., A. A. M. Alnaja, and M. R. Shaaban,
"
Recent advances in synthesis and reactions of -aminoenones (enaminones)
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Current of organic synthesis
, vol. 18, pp. 639-684, 2021.
Althagafi, I., T. A. Farghaly, E. M. H. Abbas, and M. F. Harras,
"
Benzosuberone as Precursor for Synthesis of Antimicrobial Agents: Synthesis, Antimicrobial Activity, and Molecular Docking
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POLYCYCLIC AROMATIC COMPOUNDS
, vol. 41, pp. 1646–1666, 2021.
Fawzy, A., T. A. Farghaly, A. A. A. Bahir, A. M. Hameed, A. Alharbi, and Y. A. El-Ossaily,
"
Investigation of three synthesized propane bis-oxoindoline derivatives as inhibitors for the corrosion of mild steel in sulfuric acid solutions
",
Journal of Molecular Structure
, vol. 1223 , pp. 129318, 2021.
Muhammad, Z. A., T. A. Farghaly, I. Althagafi, S. A. Al-Hussain, M. E. A. Zaki, and M. F. Harras,
"
Synthesis of antimicrobial azoloazines and molecular docking for inhibiting COVID-19
",
J Heterocyclic Chem.
, vol. 58, pp. 1286–1301, 2021.
Al-Hussain, S. A., F. Alshehrei, M. E. A. Zaki, M. F. Harras, T. A. Farghaly, and Z. A. Muhammad,
"
Fluorinated hydrazonoyl chlorides as precursors for synthesis of antimicrobial azoles
",
J Heterocyclic Chem.
, vol. 58 , pp. 589–602, 2021.
Publications
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Antimicrobial Activity of [1,2,4]Triazolo[4,3-a]pyrimidine and New Pyrido[3,2-f][1,4] thiazepine Derivatives
Antitumor activity of pyrrolizines and their Cu(II) complexes: Design, synthesis and cytotoxic screening with potential apoptosi
Biological evaluation of benzosuberones
Cholinesterase Inhibitory Activity of Some semi-Rigid Spiro Heterocycles: POM Analyses and Crystalline Structure of Pharmacophor
Indomethacin Analogs: Synthesis, Anti-inflammatory and Analgesic Activities of Indoline Derivatives
Microwave-Assisted Synthesis of Antimicrobial Agents Containing Carbazole and Thiazole Moieties
Synthesis of 8,10-disubstituted-triazoloperimidines from (E)-3-(dimethylamino)-1-(8- phenyl-8H-[1,2,4]triazolo[4,3-a]perimidin-1
Synthesis of New Bis-Spiropyrazoles as Antitumor Agents under Ultrasound Irradiation
Synthesis of Pyrazolone Derivatives and Their Nanometer Ag(I) Complexes and Physicochemical, DNA Binding, Antitumor, and Theoret
Terephthalaldehyde: An Effecient Key Precursor for Novel Synthesis of Some Interesting Bis-thiazoles and Bis-triazolopyrimidinon
file:///E:/Mostafa/Desktop/F/Thoraya/thoraya%20Reveiw/Papers%20Thoraya/2019/New%20folder/2019JHC391.pdf
file:///E:/Mostafa/Desktop/F/Thoraya/thoraya%20Reveiw/Papers%20Thoraya/2019/New%20folder/molecules-24-04009%20(1).pdf
http://www.eurekaselect.com/164007/article
http://www.eurekaselect.com/166944/article
http://www.eurekaselect.com/170178/article
http://www.eurekaselect.com/170369/article
http://www.eurekaselect.com/172873/article
https://link.springer.com/article/10.1007%2Fs11164-018-03714-y
https://link.springer.com/article/10.1007%2Fs11164-018-3594-7
https://onlinelibrary.wiley.com/doi/abs/10.1002/aoc.5099
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6539608/
https://www.ncbi.nlm.nih.gov/pubmed/30207239
https://www.sciencedirect.com/science/article/abs/pii/S0022286019304077?via%3Dihub
https://www.sciencedirect.com/science/article/abs/pii/S0167732219322287
https://www.sciencedirect.com/science/article/pii/S2405844019310370
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