Jenny‐Lee Panayides

484 total citations
29 papers, 368 citations indexed

About

Jenny‐Lee Panayides is a scholar working on Organic Chemistry, Molecular Biology and Biomedical Engineering. According to data from OpenAlex, Jenny‐Lee Panayides has authored 29 papers receiving a total of 368 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Organic Chemistry, 14 papers in Molecular Biology and 8 papers in Biomedical Engineering. Recurrent topics in Jenny‐Lee Panayides's work include Innovative Microfluidic and Catalytic Techniques Innovation (8 papers), Chemical Synthesis and Analysis (8 papers) and Synthetic Organic Chemistry Methods (7 papers). Jenny‐Lee Panayides is often cited by papers focused on Innovative Microfluidic and Catalytic Techniques Innovation (8 papers), Chemical Synthesis and Analysis (8 papers) and Synthetic Organic Chemistry Methods (7 papers). Jenny‐Lee Panayides collaborates with scholars based in South Africa, United Kingdom and United States. Jenny‐Lee Panayides's co-authors include Willem A. L. van Otterlo, Darren L. Riley, Charles B. de Koning, Manuel A. Fernandes, Margo Nell, Vanessa Steenkamp, Werner Cordier, André Stander, Christiaan W. van der Westhuyzen and Robyn L. van Zyl and has published in prestigious journals such as PLoS ONE, Tetrahedron and Molecules.

In The Last Decade

Jenny‐Lee Panayides

26 papers receiving 364 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Jenny‐Lee Panayides South Africa 12 230 123 79 62 38 29 368
Christian Pilger Germany 7 452 2.0× 84 0.7× 149 1.9× 94 1.5× 49 1.3× 7 562
Yuheng Hu China 6 241 1.0× 56 0.5× 72 0.9× 29 0.5× 15 0.4× 9 360
Ayyiliath M. Sajith India 15 496 2.2× 179 1.5× 103 1.3× 57 0.9× 41 1.1× 50 709
Samy M. Ibrahim Egypt 11 438 1.9× 99 0.8× 79 1.0× 48 0.8× 17 0.4× 26 571
M. B. Sridhara India 11 312 1.4× 140 1.1× 29 0.4× 29 0.5× 18 0.5× 20 417
Atukuri Dorababu India 14 428 1.9× 128 1.0× 54 0.7× 54 0.9× 13 0.3× 36 545
Bhupendra P. Joshi India 12 265 1.2× 79 0.6× 35 0.4× 28 0.5× 16 0.4× 27 409
Cedric Stephan Graebin Brazil 12 290 1.3× 150 1.2× 39 0.5× 23 0.4× 43 1.1× 20 466
Nguyễn Đình Thành Vietnam 13 460 2.0× 173 1.4× 80 1.0× 47 0.8× 21 0.6× 63 557
Huizhen Zhang China 8 378 1.6× 132 1.1× 34 0.4× 17 0.3× 12 0.3× 14 531

Countries citing papers authored by Jenny‐Lee Panayides

Since Specialization
Citations

This map shows the geographic impact of Jenny‐Lee Panayides'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 Jenny‐Lee Panayides with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jenny‐Lee Panayides more than expected).

Fields of papers citing papers by Jenny‐Lee Panayides

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jenny‐Lee Panayides. 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 Jenny‐Lee Panayides. The network helps show where Jenny‐Lee Panayides may publish in the future.

Co-authorship network of co-authors of Jenny‐Lee Panayides

This figure shows the co-authorship network connecting the top 25 collaborators of Jenny‐Lee Panayides. A scholar is included among the top collaborators of Jenny‐Lee Panayides 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 Jenny‐Lee Panayides. Jenny‐Lee Panayides is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
2.
Panayides, Jenny‐Lee, et al.. (2025). Revitalised Hofmann carbylamine synthesis made possible with flow chemistry. Reaction Chemistry & Engineering. 11(1). 42–48.
3.
Panayides, Jenny‐Lee, et al.. (2024). The role of silicon in drug discovery: a review. RSC Medicinal Chemistry. 15(10). 3286–3344. 44 indexed citations
4.
5.
Theron, Anjo, et al.. (2024). Evaluating Blood–Brain Barrier Permeability, Cytotoxicity, and Activity of Potential Acetylcholinesterase Inhibitors: In Vitro and In Silico Study. Pharmacology Research & Perspectives. 12(6). e70043–e70043. 2 indexed citations
6.
Panayides, Jenny‐Lee, et al.. (2023). The synthesis of bupropion hydrochloride under greener and safer conditions utilizing flow technologies. Reaction Chemistry & Engineering. 9(1). 45–57. 4 indexed citations
7.
Panayides, Jenny‐Lee, et al.. (2022). Design and testing of an ozonolysis reactor module with on-the-fly ozone degassing under flow conditions. Reaction Chemistry & Engineering. 7(8). 1718–1727. 5 indexed citations
8.
Riley, Darren L., et al.. (2022). Use of open-source software platform to develop dashboards for control and automation of flow chemistry equipment. Digital Discovery. 1(5). 596–604. 6 indexed citations
9.
Stander, André, et al.. (2022). Discovery of Novel Acetylcholinesterase Inhibitors by Virtual Screening, In Vitro Screening, and Molecular Dynamics Simulations. Journal of Chemical Information and Modeling. 62(6). 1550–1572. 17 indexed citations
10.
Pye, Dominic R., Wenyi Chen, Benjamin J. Deadman, et al.. (2022). Assessing a sustainable manufacturing route to lapatinib. Reaction Chemistry & Engineering. 7(11). 2420–2426. 2 indexed citations
11.
Riley, Darren L., et al.. (2022). The in silico and in vitro analysis of donepezil derivatives for Anopheles acetylcholinesterase inhibition. PLoS ONE. 17(11). e0277363–e0277363. 7 indexed citations
12.
Panayides, Jenny‐Lee, et al.. (2021). Rapid formation of 2-lithio-1-(triphenylmethyl)imidazole and substitution reactions in flow. Reaction Chemistry & Engineering. 6(11). 2018–2023. 3 indexed citations
13.
Riley, Darren L., et al.. (2019). Landscape and opportunities for active pharmaceutical ingredient manufacturing in developing African economies. Reaction Chemistry & Engineering. 4(3). 457–489. 17 indexed citations
14.
Cordier, Werner, Margo Nell, André Stander, et al.. (2019). Novel N-benzylpiperidine carboxamide derivatives as potential cholinesterase inhibitors for the treatment of Alzheimer's disease. European Journal of Medicinal Chemistry. 179. 680–693. 27 indexed citations
15.
Panayides, Jenny‐Lee, et al.. (2018). Immobilized tetrakis(triphenylphosphine)palladium(0) for Suzuki–Miyaura coupling reactions under flow conditions. Reaction Chemistry & Engineering. 4(2). 372–382. 10 indexed citations
16.
Cordier, Werner, Margo Nell, Christiaan W. van der Westhuyzen, et al.. (2016). Targeting Alzheimer's disease by investigating previously unexplored chemical space surrounding the cholinesterase inhibitor donepezil. European Journal of Medicinal Chemistry. 127. 671–690. 44 indexed citations
17.
Panayides, Jenny‐Lee, Véronique Mathieu, Laetitia Moreno Y Banuls, et al.. (2016). Synthesis and in vitro growth inhibitory activity of novel silyl- and trityl-modified nucleosides. Bioorganic & Medicinal Chemistry. 24(12). 2716–2724. 14 indexed citations
18.
Harmse, Leonie, et al.. (2015). Aberrant Apoptotic Response of Colorectal Cancer Cells to Novel Nucleoside Analogues. PLoS ONE. 10(9). e0138607–e0138607. 11 indexed citations
19.
Panayides, Jenny‐Lee, et al.. (2007). The Synthesis of 5-, 6-, 7- and 8-Membered Oxygen-containing Benzo-fused Rings using Alkene Isomerization and Ring-closing Metathesis Reactions. South African Journal of Chemistry. 60(1). 1–7. 2 indexed citations
20.
Panayides, Jenny‐Lee, et al.. (2007). Synthesis of Substituted 2,3‐Dihydro‐1H‐2‐benzazepines and 1,2‐Dihydroisoquinolines Using an Isomerization‐Ring‐Closing Metathesis Strategy: Scope and Limitations. European Journal of Organic Chemistry. 2007(29). 4953–4961. 31 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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