Dr. Shaima Abed Saud, a graduate of the University of Baghdad, College of Education for Pure Sciences, Ibn Al-Haytham, Department of Chemistry, Organic Chemistry. I have many researches in the field of specialization and have held many courses and workshops in various fields. My great interest is in organic diagnosis and the preparation of new compounds with pharmacological activity.
Five years of experience teaching undergraduate students the basics of using laboratory equipment in experiments and how to prepare compounds. Four years of experience in a service laboratory, diagnosing prepared compounds using various advanced devices. From 2017 to the present, experience in teaching and supervising master's students and conducting discussions for both master's and doctoral degrees, in addition to teaching undergraduate students in the specific field of specialization.
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Member of the Syndicate of Chemical Academics Member of the Afkar Educational Foundation Member of the Al-Rasikh Technical Association Member of the Arid International Platform
Preparation of new organic compounds Identification of compounds using NMR (proton and carbon-13) Measurement of biological activities, including docking
Preparation of new organic compounds Identification of compounds using NMR (proton and carbon-13) Measurement of biological activities, including docking
2007-2013: Teaching undergraduate students in the Organic Chemistry Laboratory (first stage). 2013-2017: Academic in the Service Laboratory for Research and Equipment. 2017-present: Teaching a special topic (Photochemistry and Alicyclic compounds) (fourth stage) and also teaching Organic Chemistry (second stage).This includes teaching graduate/pure Master's/organic chemistry.
Supervising the master's student (Hajar Adeeb Salem) 2022
1, 3, 4-oxadiazole-5-thion ring (2) successfully formed at position six of 2-methylphenol and five of their thioalkyl (3a-e). Furthermore 6-(5-(Aryl)-1, 3, 4-oxadiazol-2-yl)-2-methylphenol (5a-i) were formed at position six by two method. The first method was from cyclization their correspondinghydrazones (4a-e) of 2-hydroxy-3-methylbenzohydrazide (1) using bromine in glacial acetic acid. The second method was from cyclization the hydrazide with aryl carboxylic acid in the presence of phosphorusoxy chloride. The newly synthesized compounds were characterized from their IR, NMR and mass spectra. The antioxidant properties of these compounds were screened by 2, 2-Diphenyl-1-picrylhydrazide (DPPH) and ferric reducing antioxidant power (FRAP) a
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ABSTRACT: Oxadiazole ring is a heterocyclic molecule with an oxygen and two nitrogen atoms spread throughout its five-membered structure. There are four different isomers that have been discovered, Because of their wide applications in a range of sectors, including medications . Some of these biological activity are; anticonvulsant capacity, anticancer as well, antibacterial, antiviral, antifungal, antimalarial, antitubercular, anti-asthmatic, antidepressant, antidiabetic, antioxidant, antiparkinsonian, analgesic and anti-inflammatory, are just some of the therapeutic uses that have drawn attention to drug candidates containing an oxadiazole moiety. This review, we will examine the various methods of oxadiazole synthesis. The mo
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New series of 4,4'-((2-(Aryl)-1H-benzo[d]imidazole-1,3(2H)-diyl)bis(methylene))Diphenol(3a-g) was successfully synthesized from cyclization of the reduction product of bis Schiff bases (2) with aryl aldehydes bearing phenolic hydroxyl in the presence of acetic acid. The structure of these compounds was identified from FT-IR, 1H NMR, 13C NMR and EIMs. The Antioxidant capability was screened by DPPH and FRAP assays. Both assays showed antioxidant capability more than BHT as well. Compounds 3b and 3c showed antioxidant capacity slightly less than ascorbic acid. The docking study for theses compound was carried out as III DNA polymerase inhibitor. The results of docking demonstrated that the increase in hinderances around phenolic hydr
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