Gender

Male

Location

Cairo

Birthday:

September 5

I am...

Chemist

My research field or area of interest innanotechnology

Research in Abdel-Sattar S. Hamad Elgazwy Group focuses on the development metal-mediated reactions with applications in organic synthesis. We are also developing single-molecule techniques to image catalytic reactions at individual transition metal centers. These single-molecule techniques are part of a big-picture, ground-breaking project to change the way chemists think about studying chemical reaction mechanisms: by actually watching reactions live, one molecule at a time. Ultimately, we are interesting in learning about the reactivity of transition metals such that those lessons can be applied broadly to the development of new methods. These studies provide an excellent platform for testing mechanistic hypotheses and for building new fundamental understanding of metal-based reactivity. Organic and Organometallic Syntheses including Stereoselective, Aldol reactions, Michael addition and Asymmetric Catalysis were shown emphases now days. Our research group extended interestes to chemistry of butenolides & purines and Organometallic (Li, Sn, Si and Pd) & Cross Coupling & Oxidative Addition Reactions to apply for the synthesis of the highly sophisticated organic molecules having biological importance such as (anti-inflammatory & cytotoxic activity). The crystallography study of the X-ray single crystal structures of organo-palladium organo-silicon with study the 31P-NMR, [(IR, UV, MS and 1H-13C-NMR(1D&2D)] are main target.

Interest in...

Carbon Nanotube, Nanocataysis and nanoparticles of (Zn, Zr, Pd, Pt, Au, Ag)

Publication list

LIST OF PUBLICATIONS Review articles; 1.Review article; “Photochemical Transformations of 2(5H)furanones”. Ahmed I. Hashem*, Alexander Senning and Abdel-Sattar S. Hamad; Org. Prep. Proceed. Int. 1998, 30 (4), 403-427. Impact Factor = 0.742 2.Review article; “The Chemistry of Isothiazoles” Abdel-Sattar S. Hamad Elgazwy, Tetrahedron, 2003, 59, 7445-7463, and Tetrahedron report 650. IF = 2.817 3.Review article; “The Chemistry of Tricarballylic acids” Abdel-Sattar S. Hamad Elgazwy; Current Organic Chemistry, 2004, 8(14), 1405-1423. IF = 3.232 4.Review article; Utilities of some Carbon Nucleophiles in Heterocyclic Synthesis H. M. F. Madkour and A. S. H. Elgazwy*, Current Organic Chemistry, 2007, 11(10), 853-903. Impact Factor = 3.232 5.Review Article; Overview of the Environmental Impacts of the uses of Coal, Thermal, Hydroelectricity, Oil, Gas, Fuel & Wood etc. In Pakistan, Abdel-Sattar S. Hamad Elgazwy* and Muhammad Iqbal Bhanger, Global Journal of environmental Research 2007, 1(1), 1-6. 6.Perspective; Message to the Smokers “Chemistry of tobacco smoke and Lipoprotein Atherosclerosis” Abdel-Sattar S. Hamad Elgazwy, Published in Chemweb.com, 2005; see this web site for publication http://www.chemweb.com/forum/news_item.2005-12-14.4399408439/?searchterm=None Research Articles; 7.Synthesis and Biological Activity of Some Semicarbazides, Pyridazinones and Triazoles Bearing Furan Nuclei. El-Kafrawy, A. F.; Youssef, A. S.; Hamad, A. S. and Hashem, A. I.* Egypt. J. Pharm. Sci., 1993, 34(1-3), 159-70. (Chem. Abstract. 121:297004). Impact Factor = 0.52 8.Studies of the Behavior of 2(3H) Furanthione and Thionopyrroline Derivatives toward some Nitrogen Nucleophiles. Abdel-Sattar S. Hamad*, Hashem, A. I.; El-Kafrawy, A. F. and Saad, M. M., Phosphorus, Sulfur and Silicon, 2000, 159, 157-169. Impact Factor = 0.52 9 An NMR Method for Determination of Configuration of -Substituted Carboxylic Acids. Thomas R. Hoye*, Abdel-Sattar S. Hamad, Dmitry O. Koltun, and Manomi A. Tennakoon, Tetrahedron Lett. 2000, 41, 2289-2293. Impact Factor = 2.509 10 Synthesis of arylcarbinols or arylketones end capped thiophene and Bithiophene Abdel-Sattar S. Hamad Phosphorus, Sulfur and Silicon, 2001, 170, 65-74. IF = 0.52 11 New and Convenient Synthesis of (R) and (S) of 2-methyl-3-oxa-5-(tert-butyldiphenyl silyloxyl)methylpentanoate and 2-methyl-3-oxa-5-(tert-butyldimethylsilyloxyl)methyl pentanoate. Abdel-Sattar S. Hamad* and Dieter Schinzer Phosphorus, Sulfur and Silicon, 2000, 158, 187-199. Impact Factor = 0.52 12 Studies of (Pdo-Mediated) Stille Cross-Coupling Reactions of Thiophene stannane with Aryl halide Derivatives. Abdel-Sattar S. Hamad Elgazwy. Phosphorus, Sulfur and Silicon, 2000, 164, 131-143. Impact Factor = 0.52 13 Facile Synthesis of (R,R) and of (R,S) Tricarballylic Acid Anhydride and Imide Derivatives. Abdel-Sattar S. Hamad Elgazwy, Molecules 2000, 5, 665-673. IF = 0.841 14 A facile method for the synthesis of 6-aryl-1-(3-chloropropanoyl)-4-[(E)-1-(2-furyl) methylidene]-1,2,3,4-tetrahedro-3-pyridazinones and 2-(2-chloroethyl)-5-[-aracyl--(2-furyl)]-(E)-vinyl-1,3,4-Oxadiazoles Abdel-Sattar S. Hamad* and Ahmed I. Hashem, Molecules, 2000, 5, 895-907.Impact Factor = 0.841 15 A convenient Synthesis of 4-(5-Nonanyloxycarbonyl)-3-Substituted Butanoic acids and Methyl esters Analogs of Sphingosine. Abdel-Sattar S. Hamad, Afinidad, 2001, 58, no.(493), pp. 225-230. Impact Factor = 0.188 16 Synthesis and Biological Activity of 2-Thiono-[1H]-5-Spirocyclohexylimidazo[4,3-b] Quinazolone and 8-Azaquinazolone Derivatives” Abdel-Sattar S. Hamad* and Mohamed E. Azab, Phosphorus, Sulfur and Silicon, 2001, 173, 105-114.IF= o.52 17 A New Synthesis of 4-Cyano-1,3-dihydro-2-oxo-2H-imidazole-5-(N1-tosyl) carboxamide: A Reactive Precursor for ThioPurine Analogs Abdel-Sattar S. Hamad* and H. A. Y. Derbala, Journal of Heterocyclic Chemistry 2001, 38, 939-944. IF = 0.776 18 Synthetic Approaches to pyridazine-3-one and 1,3,4-oxadiazole derivatives Abdel-Sattar S. Hamad* and Ahmed I. Hashem, Acta. Chim. Solv. 2001, 48, 431-437. IF = 0.703 19 Conversion of 3-aryl-5-phenyl-2(3H)-Furanones into 3(2H)-isothiazolone derivatives Hamed A. Derbala*, Abdel-Sattar S. Hamad, Waleed A. Elsayed and Ahmed I. Hashem, Phosphorus, Sulfur and Silicon, 2001, 175, 153-162. IF= 0.52 20 Separation of triorganomonstannanyl-and bis(triorganobistannanyl) bithiophene. Abdel-Sattar S. Hamad Elgazwy, Phosphorus, Sulfur and Silicon, 2001, 175, 237-242. IF = 0.52 21 Behavior Studies of 2(3H)-Furanones and 2(5H)-Furanones towards Some Nitrogen Nucleophiles. Abdel-Sattar S. Hamad*, Hamed A. Derbala, Waleed A. Elsayed and Ahmed I. Hashem, Acta. Chim. Solv. 2001, 48, 417-425. IF = 0.703 22 Medicinal Chemistry "Synthesis and biological activity of 2-thiono-(1H)-5-spirocyclohexylimidazo(4,3-b) quinazolone derivatives." Abdel-Sattar S. Hamad* and Mohamed E. Azab, Bollettino Chimico Farmaceutico, 2001, vol. 140, no. 4, pp. 233-237. 23 Synthetic Approaches of 4-[(E)-2-Furyl)-Methylidene]-1-(p-Toluenesulfonyl formamido)-1,2,3,4-Tetrahyd ro-3-Pyridazinones and 2-(p-Toluenesulfonylamino)-5-[alpha-Aracyl-beta-(2-Furyl)]-(E)-Vinyl-1,3,4-Oxadiazoles Elgazwy, A.-S. S. H.; Hashem, A. I. Afinidad, 2001, no. 496, pp. 449-454. Impact Factor = 0.188 24 Novel Synthesis of N-{6-Aryl-4-[(E)-2-furylmethylene]-1,2,3,4-tetrahydro-3-oxopyridazin-1-ylcarbonyl}-p-toluenesulfonamidesand and N-{5-[(E)-1-Aroylmethyl-2-(2-furyl)vinyl]-1,3,4-oxadiazol-2-yl}-p-toluenesulfonamides, Abdel-Sattar S. Hamad* and Ahmed I. Hashem J. Heterocyclic Chemistry 2002, 39, 1195-1200. Impact Factor = 0.776 25 Reactivity of Pyridazin-3(2H)-thiones, N. G. Kandile; H. T. Zaky; M. I. Mohamed and Abdel-Sattar S. Hamad Elgazwy* Heteroatom Chemstry 2003, 14(4), 335-341. Impact Factor = 0.838 26 Conversion of 2(3H)-Furannes bearing indole nuclei into novel Amide, Pyrrolone and Imidazole of N-Acetyloxindole Derivatives, Abdel-Sattar S. Hamad*, H. T. Zaky, M. I. Mohamed, H. M. Ahmed and N. G. Kandil, Heteroatom Chemistry 2003, 14(5), 434-442. Impact Factor = 0.838 27 Conversion of 2(3H)-Furanones into 1,3,4-Oxadiazoles Abdel-Sattar S. Hamad Elgazwy,* Mayssoune Y. Zaki, Nahed N. Eid and Ahmed I. Hashem Heteroatom Chemistry 2003, 14 (6), 570-574. Impact Factor = 0.838 28 2,2´-Bithiophene-5,5´-Tetrahydroisoquinoline as Michellamine Analogs. Abdel-Sattar S. Hamad Elgazwy, Journal of Sulfur Chemistry, 2004, 25, 257-282. Impact Factor = 0.52 29 Improved Studies of Cross-Coupling Reactions of 5- (tri-n-butystannyl)- and 5,5’-bis(tri-n-butylstannyl)-2,2’-Bithiophene with Aryl halides. Abdel-Sattar S. Hamad Elgazwy, Journal of Heterocyclic Chemistry 2004, 41, 755-759. IF = 0.776 30 Stille Coupling of Thiophene with Tetrahydroisoquinoline alkaloid; Abdel-Sattar S. Hamad Elgazwy Mendeleev Communications, 2006, 16(2), 92-94. IF = 0.712 31 Synthetic Analogs of Dioncophylline and Michellamine by Stille Coupling Abdel-Sattar S. Hamad Elgazwy, Journal of Heterocyclic Chemistry 2006, 43, 1151-1156. IF = 0.776 32 “2(3H)-Furanones as Synthons for Novel Polyamide of 1,3-Diazines and 1,3,5-Triazines”; Abdel-Sattar S. Hamad Elgazwy,*1 H. T. Zaky, M. I. Mohamed and N. G. Kandile2, ARKIVOC e-Journal of Organic Chemistry 2006, (X), 162-172. IF = 0.8 33 Novel Synthesis of Spiro-thiopyrano[2,3-d]thiazolidines Abdel-Sattar S. Hamad Elgazwy*, Saad R. Atta-Allah, Masoom Yasinzai, Sarah M. Mandel and Jaanette A. Krause Bauer; Mendeleev Communications. 2006, 16(5), 267-270. IF = 0.712 34 A Novel Potentiometric Membrane Sensor Based on Aryl Palladium Complex for Selective Determination of Thiocyanate in the Saliva and Urine of Cigarette Smokers. Saad S.M. Hassan,* Wagiha H. Mohmoud, Abdel-Sattar S. Hamad Elgazwy, Nahla M. Badawy, Electroanalysis, 2006, 18(21), 2070-2078. IF = 2.444 35 Reactions of 2(3H)- and 2(5H)-Furanones having no exocyclic double bonds with Some Nitrogen Nucleophiles. Ahmed I. Hashem *, Nabil M. Youssef, Hamed A. Derbala, Abdel-Sattar S. Hamad, Hayam H. Sayed and Waleed A. Elsayed, accepted for publication in Egypt. J. Chem., 2006, 49 (6), 443-447. IF = 36 Synthesis and Reactivity of Thiophene Palladium and thiophene Dipalladium complexes with Unsaturated Molecules; Abdel-Sattar S. Hamad Elgazwy( (accepted for publication in Applied Organometallic Chemistry, 2007, 21(12), 1041-1053 . IF = 1.233 37 “Synthesis and Reactivity of Isoindigo: A Revisit” Abdel-Sattar S. Hamad Elgazwy* and Saad R. Atta-Allah, galley proof published in Afinidad, 2008, 65,535, pp. 148-155. IF = 0.188 38 Synthesis and Characterization of Pyrido[1,2-a]Quinoline Palladacycles Abdel-Sattar S. Hamad Elgazwy Monatshefte für Chemie / Chemical Monthly, 2008, 139 (11), 1285-1297. Impact Factor = 0.974 39 “Sensitivity of Kinetoplastids to Aminoglycoside correlation with the 3’ small subunit rRNA gene,” M. Masoom Yasinzai and Abdel-Sattar S. Hamad Elgazwy*. (Truk. J. Biol., 2008, 32(3); 167-174. Impact Factor = 0.646 40 Conversion of Iminoacyl Quinolinylpalladium (II) Complexes into Novel Oxo-pyrrolo[3,4-b]Quinolines via Depalladation ReactionsAbdel-Sattar S. Hamad Elgazwy* and Saad R. Atta-Allah, submitted to J. Org. Chem., 2008. IF = 3.79 41 Synthesis of 5-SpiroCyclohexyl-2,4-Dithiohydantoin Derivatives with Expected Antimicrobial Activities, Abdel-Sattar S. Hamad Elgazwy*a, Saad R. Atta-Allaha and Sherif M.A.S. Keshkb, Monatshefte für Chemie / Chemical Monthly, 2009, 140 (2), 243-249. Impact Factor = 0.974 42 “Conversion of novel palladacycles into oxo-pyrrolo[3,4-b]quinolines Abdel-Sattar S. Hamad Elgazwy, polyhedron 2009, 28, 349-359. IF = 1.78 43 Synthesis and Characterization of Novel Five- Membered palladacycles”Abdel-Sattar S. Hamad Elgazwy Polyhedron 2009, 28, 3667-3674. IF = 1.78 44 Synthesis and Thermograms Chemical Study on Complexes of Nickel (II)-, Chromium (III)- and Europium (III)- Tricarballylic acid (TCA) moiety of Mycotoxin Natural products Abdel-Sattar S. Hamad Elgazwy,* Mostafa H. Khalil, and Eman Hamed accepted on Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry, Corrected Proof, Available online, 2009, XX, XX

Researchgroup, Institute, University, School, Company name

Organometallics Group, Department of Chemistry (Faculty of Science, Ain Shams University

Researchgroup, Institute, Company, University, School webpage

https://sci.shams.edu.eg/

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