ziad moussa
United Arab Emirates University, Texas A&M University
Research areas: Chemistry · Organic Chemistry · Crystal structures of chemical compounds · Synthesis and biological activity · Crystallography and molecular interactions
0000-0002-3365-0451
About
Ziad undertook his undergraduate and postgraduate studies in chemistry at University of Calgary. His Ph.D. research was conducted under the supervision of prof. Thomas G. Back and focused on the synthesis and evaluation of some novel selenium-based chiral auxiliaries and glutathione peroxidase mimetics. His postdoctoral studies were done at Texas A&M University in the laboratories of Prof. Daniel Romo. His main research interests include the development of synthetic methodologies and the synthesis and characterization of novel bioactive organic/heterocyclic compounds with anticancer, antiviral, and antimicrobial activities.
Employment
- 2023 - Present
-
Texas A&M University research associate2003 - 2006
Education
Education history is unavailable.
Projects & Funding
Projects & funding information is unavailable.
Publications (109)
- Sustainable assembly of quinazolinones via iodine-mediated/catalyzed methods: a decennial update on transition-metal-free approaches Save
- Synthesis of novel bis(6-ethyl-4-hydroxy-2H-chromen-2-one) derivatives as potential acetylcholinesterase and monoamine oxidase inhibitors Save
- Intramolecular NN Bond Formations to Access N‐Heterocycles Under Transition Metal‐Free Conditions Save
- Synthesis, cytotoxicity, and molecular docking studies of novel selenourea-embedded quinoline and benzimidazole derivatives against MDA-MB-231 and A549 cancer cell lines Save
- Diazo retention transformations of aryldiazonium salts towards nitrogen rich heterocycles Save
- Innovative regioselective synthesis of dispiro[fluorene-9,3′-pyrazole-5′,4″-pyrazolidines]: experimental and computational study Save
- Synthesis and Computational Analysis of Novel Carboximidamide/ Benzothiazole and 1,2,4-Oxadiazole/Benzothiazole Hybrid Compounds for Biological Applications Save
- Study of 1,3-Dipolar Cycloaddition Between 4-Acyl-1H-pyrrole-2,3-diones Fused at the [e]-Side with a Heterocyclic Moiety and Diphenylnitrone: A Comprehensive MEDT, Docking Approach and MD Simulation Save
- High nonlinear optical performance of p-tert-butylthiacalix[4]arene derivatives: Synthesis, characterization, and theoretical validation Save
- The influence of the pyridyl substituent in N-methyl-P,P-diphenyl-N-2-pyridinyl-phosphinous amide ligand on the coordination chemistry of group 6B metal carbonyl derivatives Save
- Effect of vanadium (V) doping on the physical characteristics of novel n-type TiO2 for sustainable energy storage Save
- Novel C-3 and C-20 derived analogs of betulinic acid as potent cytotoxic agents: design, synthesis, in vitro and in silico studies Save
- Transition-metal-free approaches to access N-heterocycles and valuable intermediates from aryldiazonium salts Save
- Recent Progress in the Synthesis of Benzoxazin-4-Ones, Applications in N-Directed Ortho-Functionalizations, and Biological Significance Save
- Design and DFT calculations of optoelectronic material based on thiazolobenzimidazole-coupled isatin derivatives Save
- Recent highlights in the synthesis and biological significance of pyrazole derivatives Save
- Exclusive Solvent-Controlled Regioselective Catalytic Synthesis of Potentially Bioactive Imidazolidineiminodithiones: NMR Analysis, Computational Studies and X-ray Crystal Structures Save
- Design, synthesis and preliminary antibacterial evaluation of novel 1,3-benzoxazole/carboximidamide- and 1,3-benzoxazole/3-aryl-1,2,4-oxadiazole hybrids Save
- Study on Regio- and Diastereoselectivity of the 1,3-Dipolar Cycloaddition Reaction of Azomethine Ylide with 2-(Benzo[d]thiazol-2-yl)-3-(aryl)acrylonitrile: Synthesis, Spectroscopic, and Computational Approach Save
- Design, synthesis, molecular docking, ADMET studies, and biological activity evaluation of new 2-({[3-aryl-1,2,4-oxadiazol-5-yl)methyl]thio}-1H-benzimidazoles and 6-amino-6-aryl-5,6-dihydro[1,6,2,4]oxathiadiazocino[4,5-a]benzimidazol-3(2H)-ones Save