Farhat Rezgui

671 total citations
44 papers, 477 citations indexed

About

Farhat Rezgui is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, Farhat Rezgui has authored 44 papers receiving a total of 477 indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Organic Chemistry, 8 papers in Molecular Biology and 5 papers in Inorganic Chemistry. Recurrent topics in Farhat Rezgui's work include Asymmetric Synthesis and Catalysis (23 papers), Chemical Synthesis and Reactions (13 papers) and Synthetic Organic Chemistry Methods (9 papers). Farhat Rezgui is often cited by papers focused on Asymmetric Synthesis and Catalysis (23 papers), Chemical Synthesis and Reactions (13 papers) and Synthetic Organic Chemistry Methods (9 papers). Farhat Rezgui collaborates with scholars based in Tunisia, France and Saudi Arabia. Farhat Rezgui's co-authors include M. M. EL GAIED, Pierre Mangeney, Hassen Amri, Jalloul Bouajila, Ali Gargouri, Wafa Mihoubi, Giovanni Poli, Khadija Essafi‐Benkhadir, Issam Ben Salem and Hadda‐Imene Ouzari and has published in prestigious journals such as The Journal of Organic Chemistry, Tetrahedron and Tetrahedron Letters.

In The Last Decade

Farhat Rezgui

42 papers receiving 464 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Farhat Rezgui Tunisia 11 408 95 76 24 24 44 477
Gustavo Moura‐Letts United States 13 373 0.9× 162 1.7× 39 0.5× 47 2.0× 28 1.2× 29 479
Lorenzo V. White China 12 249 0.6× 108 1.1× 31 0.4× 31 1.3× 15 0.6× 39 342
Luísa C. R. Carvalho Portugal 9 412 1.0× 158 1.7× 52 0.7× 55 2.3× 19 0.8× 17 526
Ramesh Deshidi India 11 330 0.8× 156 1.6× 52 0.7× 87 3.6× 23 1.0× 13 525
Francisco Bermejo Spain 15 304 0.7× 125 1.3× 49 0.6× 69 2.9× 13 0.5× 30 463
L. D. Konyushkin Russia 14 547 1.3× 180 1.9× 36 0.5× 67 2.8× 25 1.0× 72 666
D. S. Iyengar India 14 386 0.9× 185 1.9× 103 1.4× 21 0.9× 15 0.6× 62 512
Alic Barbă Moldova 11 226 0.6× 112 1.2× 32 0.4× 39 1.6× 14 0.6× 54 314
Rajesh H. Tale India 13 628 1.5× 183 1.9× 64 0.8× 70 2.9× 19 0.8× 23 734
Young Soo Gyoung Japan 11 492 1.2× 149 1.6× 132 1.7× 13 0.5× 15 0.6× 16 565

Countries citing papers authored by Farhat Rezgui

Since Specialization
Citations

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

Fields of papers citing papers by Farhat Rezgui

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Farhat Rezgui. 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 Farhat Rezgui. The network helps show where Farhat Rezgui may publish in the future.

Co-authorship network of co-authors of Farhat Rezgui

This figure shows the co-authorship network connecting the top 25 collaborators of Farhat Rezgui. A scholar is included among the top collaborators of Farhat Rezgui 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 Farhat Rezgui. Farhat Rezgui 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
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Khemakhem, Bassem, Ikram Ben Amor, Jalel Gargouri, et al.. (2024). Antiplatelet activity and toxicity profile of novel phosphonium salts derived from Michael reaction. European Journal of Pharmaceutical Sciences. 194. 106692–106692. 3 indexed citations
3.
Aifa, Sami, et al.. (2023). New Morita-Baylis-Hillman (MBH) phosphonium salts from alcohols to the synthesis of 2-alkenyl- and 2-alkylidenecyclohexenones. Journal of Molecular Structure. 1286. 135532–135532. 1 indexed citations
4.
Zid, Mohamed Faouzi, et al.. (2023). Synthesis, crystal structure, spectroscopic, and Hirshfeld surface study of a new functionalized α-hydroxyphosphonate complex of tin(IV) chloride. Phosphorus, sulfur, and silicon and the related elements. 198(12). 1002–1008. 1 indexed citations
5.
Salem, Issam Ben, et al.. (2023). Antimicrobial Activities and Mode of Flavonoid Actions. Antibiotics. 12(2). 225–225. 32 indexed citations
6.
Bouajila, Jalloul, et al.. (2023). Metal catalyst-free N-allylation/alkylation of imidazole and benzimidazole with Morita–Baylis–Hillman (MBH) alcohols and acetates. Beilstein Journal of Organic Chemistry. 19. 1251–1258.
7.
8.
Rezgui, Farhat, et al.. (2020). Bi(OTf)3-catalysed regioselective arylation of Morita-Baylis-Hillman type allylic electrophiles. Tetrahedron Letters. 61(15). 151758–151758. 4 indexed citations
9.
Mihoubi, Wafa, et al.. (2018). Anti-melanogenesis potential of a new series of Morita-Baylis-Hillman adducts in B16F10 melanoma cell line. Bioorganic Chemistry. 84. 17–23. 13 indexed citations
10.
Mihoubi, Wafa, et al.. (2018). Potential antioxidant activity of Morita-Baylis-Hillman adducts. Bioorganic Chemistry. 78. 24–28. 25 indexed citations
11.
Bouajila, Jalloul, et al.. (2017). Palladium-catalyzed nucleophilic allylic substitution of Morita–Baylis–Hillman adducts with enamines: Synthesis of 1,5-dicarbonyl compounds. Comptes Rendus Chimie. 20(5). 484–491. 4 indexed citations
12.
Bouajila, Jalloul, et al.. (2017). Chemoselective reaction of ethane-1,2-dithiol, hydrazines, and hydroxylamine onto γ-keto allyl phosphonates and phosphine oxides. ARKIVOC. 2017(4). 265–272. 4 indexed citations
13.
Rezgui, Farhat, et al.. (2017). Transition metal-free direct nucleophilic α-substitution of Morita–Baylis–Hillman alcohols with amines and thiols. Synthetic Communications. 47(9). 892–898. 1 indexed citations
14.
Mahmoudi, Salah, et al.. (2017). Geochemical characteristics and reservoir continuity of Silurian Acacus in Ghadames Basin, Southern Tunisia. Journal of African Earth Sciences. 135. 14–23. 7 indexed citations
15.
Rezgui, Farhat, et al.. (2016). Et3B-mediated and palladium-catalyzed direct allylation of β-dicarbonyl compounds with Morita–Baylis–Hillman alcohols. Beilstein Journal of Organic Chemistry. 12. 2402–2409. 4 indexed citations
16.
Vrancken, Emmanuel, et al.. (2016). First DMAP-mediated direct conversion of Morita–Baylis–Hillman alcohols into γ-ketoallylphosphonates: Synthesis of γ-aminoallylphosphonates. Beilstein Journal of Organic Chemistry. 12. 2906–2915. 5 indexed citations
17.
Rezgui, Farhat, et al.. (2016). A Metal‐Free Synthesis of 2‐Alkyl(or Aryl) Thiomethyl‐2‐cyclohexenones from Cyclic Morita–Baylis–Hillman Bromides. Helvetica Chimica Acta. 99(9). 704–709. 2 indexed citations
18.
Rezgui, Farhat, et al.. (2014). General and Efficient Transesterification ofβ-Keto Esters with Various Alcohols Using Et3N as a Brønsted Base Additive. Synthetic Communications. 44(22). 3320–3327. 10 indexed citations
19.
Rezgui, Farhat, et al.. (1999). Asymmetric synthesis of 1,2- and 1,4-dihydroquinolines. Tetrahedron Letters. 40(34). 6241–6244. 39 indexed citations
20.
Rezgui, Farhat & M. M. EL GAIED. (1998). DMAP-catalyzed hydroxymethylation of 2-cyclohexenones in aqueous medium through Baylis-Hillman reaction. Tetrahedron Letters. 39(33). 5965–5966. 132 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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