George M. Iskander

778 total citations
51 papers, 626 citations indexed

About

George M. Iskander is a scholar working on Organic Chemistry, Molecular Biology and Microbiology. According to data from OpenAlex, George M. Iskander has authored 51 papers receiving a total of 626 indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Organic Chemistry, 22 papers in Molecular Biology and 7 papers in Microbiology. Recurrent topics in George M. Iskander's work include Bacterial biofilms and quorum sensing (11 papers), Antimicrobial Peptides and Activities (7 papers) and Phenothiazines and Benzothiazines Synthesis and Activities (6 papers). George M. Iskander is often cited by papers focused on Bacterial biofilms and quorum sensing (11 papers), Antimicrobial Peptides and Activities (7 papers) and Phenothiazines and Benzothiazines Synthesis and Activities (6 papers). George M. Iskander collaborates with scholars based in Australia, Sudan and Singapore. George M. Iskander's co-authors include Naresh Kumar, David StC. Black, Stuart A. Rice, Afaf Kamal‐Eldin, Mark Willcox, Kitty K. K. Ho, Samuel K. Kutty, Nicolas Barraud, Renate Griffith and Thomas P. Davis and has published in prestigious journals such as Biomaterials, Journal of Medicinal Chemistry and Polymer.

In The Last Decade

George M. Iskander

48 papers receiving 607 citations

Peers

George M. Iskander

MICRO

Giulia Martelli Italy

Florian Kloß Germany

Rokuro Okamoto Japan

Ivana Aleksić Serbia

Markus Oberthür Germany

Ponmani Jeyakkumar China

Madison H. Fletcher United States

Nazira Karodia United Kingdom

Carmen Limban Romania

Chantal Finance France

Giulia Martelli Italy

George M. Iskander

414 ×1.3

419 ×1.5

54 ×0.8

MICRO

39 ×0.6

18 ×0.4

Citations per year, relative to George M. Iskander George M. Iskander (= 1×) peers Giulia Martelli

Countries citing papers authored by George M. Iskander

Since Specialization

Citations

This map shows the geographic impact of George M. Iskander's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by George M. Iskander with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites George M. Iskander more than expected).

Fields of papers citing papers by George M. Iskander

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by George M. Iskander. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by George M. Iskander. The network helps show where George M. Iskander may publish in the future.

Co-authorship network of co-authors of George M. Iskander

This figure shows the co-authorship network connecting the top 25 collaborators of George M. Iskander. A scholar is included among the top collaborators of George M. Iskander based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with George M. Iskander. George M. Iskander is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Yu, Tsz Tin, George M. Iskander, Daniel Shiu‐Hin Chan, et al.. (2019). Dihydropyrrolones as bacterial quorum sensing inhibitors. Bioorganic & Medicinal Chemistry Letters. 29(9). 1054–1059. 30 indexed citations

Biswas, Nripendra Nath, et al.. (2018). Alkyne-Substituted Fimbrolide Analogues as Novel Bacterial Quorum-Sensing Inhibitors. Australian Journal of Chemistry. 71(9). 708–715. 9 indexed citations

Nizalapur, Shashidhar, Nripendra Nath Biswas, Kitty K. K. Ho, et al.. (2018). Design and Synthesis of Lactams Derived from Mucochloric and Mucobromic Acids as Pseudomonas aeruginosa Quorum Sensing Inhibitors. Molecules. 23(5). 1106–1106. 19 indexed citations

Iskander, George M., et al.. (2015). Ritter reactions of isoflavanols: a facile route to 4-amidoisoflavans. Tetrahedron Letters. 56(15). 1941–1943. 2 indexed citations

Yee, Eugene, et al.. (2013). Synthesis of novel isoflavene–propranolol hybrids as anti-tumor agents. Bioorganic & Medicinal Chemistry. 21(7). 1652–1660. 22 indexed citations

Ho, Kitty K. K., Renxun Chen, Mark Willcox, et al.. (2013). Quorum sensing inhibitory activities of surface immobilized antibacterial dihydropyrrolones via click chemistry. Biomaterials. 35(7). 2336–2345. 32 indexed citations

Kutty, Samuel K., Mohan Bhadbhade, George M. Iskander, et al.. (2010). Fimbrolide disulfanes: synthesis and crystal interactions. Tetrahedron Letters. 51(37). 4856–4858. 4 indexed citations

Iskander, George M., et al.. (2007). An Efficient Lactamization of Fimbrolides to Novel 1,5‐Dihydropyrrol‐2‐ones.. ChemInform. 38(29). 1 indexed citations

Iskander, George M., et al.. (2000). Synthesis and copolymerization of methacryloyl hydroxamic acids. Journal of Applied Polymer Science. 78(4). 751–758. 7 indexed citations

10.

Iskander, George M., et al.. (1998). Synthesis and polymerization of new pyrrolidone-containing methacrylate monomers. Polymer. 39(17). 4165–4169. 23 indexed citations

11.

Iskander, George M., et al.. (1996). Synthesis and properties of poly(1‐alkyl‐3‐methylene‐2‐pyrrolidone)s. Macromolecular Chemistry and Physics. 197(10). 3123–3133. 14 indexed citations

12.

Kamal‐Eldin, Afaf, et al.. (1992). Seed lipids of Sesamum indicum and related wild species in Sudan. The sterols. Journal of the Science of Food and Agriculture. 59(3). 327–334. 49 indexed citations

13.

Iskander, George M., et al.. (1990). Mononuclear Benzoylhydrazide Complexes of Cu²⁺, Fe³⁺ and V⁵⁺O and Fe²⁺ sulphate. Single crystal X‐ray and E.P.R. data of the Cu²⁺ complex. Journal für praktische Chemie. 332(3). 293–299. 4 indexed citations

14.

Iskander, George M., et al.. (1988). Crystal and Molecular Structure of Ambrosin and Damsin, sesquiterpene lactone isolates of Ambrosia maritima L. Journal für praktische Chemie. 330(2). 182–190. 7 indexed citations

15.

Gilchrist, T. L., et al.. (1985). Acid-catalysed rearrangement of 3-acyl-6-alkoxy-5,6-dihydro-4H-1,2-oxazines: a route to 3-alkoxypyridine 1-oxides. Journal of the Chemical Society Perkin Transactions 1. 2769–2769. 12 indexed citations

16.

Ferguson, George, et al.. (1983). An unusual furan cycloadduct from N-phenylbetaine and dimethyl acetylenedicarboxylate. The crystal and molecular structure of dimethyl 5-(3-N-phenyliminoprop-1-enyl)furan-2,3-dicarboxylate. Journal of the Chemical Society Chemical Communications. 1216–1216. 3 indexed citations

17.

Gilchrist, T. L. & George M. Iskander. (1982). 1H-1,4-benzothiazines. New cyclic sulphonium ylides. Journal of the Chemical Society Perkin Transactions 1. 831–831. 5 indexed citations

18.

Hussein, Mohammed A., et al.. (1982). Solutions in selenic acid. Part 9. Higher acids of selenic acid; the SeO₃–H₂SeO₄system. Journal of the Chemical Society Dalton Transactions. 1645–1648. 2 indexed citations

19.

Iskander, George M.. (1973). Formation of styrene derivatives from dibromocarbene adducts of cyclohexa-1,4-dienes. Journal of the Chemical Society Perkin Transactions 1. 2202–2202. 1 indexed citations

20.

Iskander, George M., et al.. (1965). 243. 4-Hydroxybenzocyclobuten-1-one and its derivatives. Journal of the Chemical Society (Resumed). 1390–1390. 7 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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