Gaëlle Chouraqui

1.0k total citations
28 papers, 822 citations indexed

About

Gaëlle Chouraqui is a scholar working on Organic Chemistry, Molecular Biology and Biotechnology. According to data from OpenAlex, Gaëlle Chouraqui has authored 28 papers receiving a total of 822 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Organic Chemistry, 4 papers in Molecular Biology and 4 papers in Biotechnology. Recurrent topics in Gaëlle Chouraqui's work include Synthetic Organic Chemistry Methods (16 papers), Catalytic Alkyne Reactions (8 papers) and Cyclopropane Reaction Mechanisms (8 papers). Gaëlle Chouraqui is often cited by papers focused on Synthetic Organic Chemistry Methods (16 papers), Catalytic Alkyne Reactions (8 papers) and Cyclopropane Reaction Mechanisms (8 papers). Gaëlle Chouraqui collaborates with scholars based in France, United Kingdom and Netherlands. Gaëlle Chouraqui's co-authors include Jean‐Luc Parrain, Laurent Comméiras, Max Malacrìa, Corinne Aubert, Marc Petit, P Colonna, Olivier Chuzel, Phannarath Phansavath, Gordon J. Florence and Kate Ashton and has published in prestigious journals such as Journal of the American Chemical Society, Chemical Society Reviews and Angewandte Chemie International Edition.

In The Last Decade

Gaëlle Chouraqui

27 papers receiving 810 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gaëlle Chouraqui France 18 724 119 61 59 56 28 822
Toshiyuki Hamura Japan 19 915 1.3× 66 0.6× 38 0.6× 32 0.5× 54 1.0× 56 984
Yoshizumi Yasui Japan 16 997 1.4× 156 1.3× 145 2.4× 38 0.6× 61 1.1× 36 1.0k
Veejendra K. Yadav India 22 1.3k 1.8× 167 1.4× 92 1.5× 46 0.8× 34 0.6× 60 1.4k
Philippe A. Peixoto France 20 658 0.9× 125 1.1× 61 1.0× 70 1.2× 52 0.9× 42 812
Yingbo Shi China 13 442 0.6× 106 0.9× 21 0.3× 54 0.9× 65 1.2× 28 542
Jörg P. Hehn Germany 10 1.1k 1.6× 159 1.3× 170 2.8× 59 1.0× 43 0.8× 12 1.3k
M. Montserrat Martı́nez Spain 17 537 0.7× 111 0.9× 46 0.8× 21 0.4× 42 0.8× 37 637
Stephen P. Lathrop United States 8 690 1.0× 62 0.5× 128 2.1× 35 0.6× 41 0.7× 9 762
Tapas Das India 15 530 0.7× 85 0.7× 62 1.0× 41 0.7× 41 0.7× 44 587
Andrea Vescovi Germany 9 669 0.9× 262 2.2× 80 1.3× 140 2.4× 76 1.4× 10 844

Countries citing papers authored by Gaëlle Chouraqui

Since Specialization
Citations

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

Fields of papers citing papers by Gaëlle Chouraqui

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gaëlle Chouraqui

This figure shows the co-authorship network connecting the top 25 collaborators of Gaëlle Chouraqui. A scholar is included among the top collaborators of Gaëlle Chouraqui 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 Gaëlle Chouraqui. Gaëlle Chouraqui 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.
Colonna, P, et al.. (2025). Formation of Substituted Benzocyclobutenes Starting from Donor–Acceptor Cyclopropanes. The Journal of Organic Chemistry. 90(11). 4115–4120.
2.
Giorgi, Michel, et al.. (2024). Template-Directed In Crystallo Photopolymerization of a Donor–Acceptor Cyclopropane: When Everything Falls into Place!. Journal of the American Chemical Society. 146(25). 17384–17392. 4 indexed citations
3.
Rodriguez, Jean, et al.. (2024). Enantioselective Synthesis of Heteroatom‐Linked Non‐Biaryl Atropisomers. Angewandte Chemie International Edition. 63(30). e202407767–e202407767. 25 indexed citations
4.
Naubron, Jean‐Valère, et al.. (2023). Designing Donor‐Acceptor Cyclopropane for the ThermalSynthesis of Carbocyclic Eight‐Membered Rings. Advanced Synthesis & Catalysis. 365(7). 1002–1011. 5 indexed citations
5.
Parrain, Jean‐Luc, et al.. (2023). Stereoselective formation of boron-stereogenic organoboron derivatives. Chemical Society Reviews. 52(13). 4381–4391. 34 indexed citations
6.
Colonna, P, et al.. (2021). Small rings in the bigger picture: ring expansion of three- and four-membered rings to access larger all-carbon cyclic systems. Chemical Society Reviews. 50(13). 7513–7538. 91 indexed citations
7.
Nava, Paola, et al.. (2019). Highly diastereoselective preparation of chiral NHC-boranes stereogenic at the boron atom. Chemical Science. 10(26). 6524–6530. 25 indexed citations
8.
Parrain, Jean‐Luc, et al.. (2017). Intriguing Electrophilic Reactivity of Donor–Acceptor Cyclopropanes: Experimental and Theoretical Studies. European Journal of Organic Chemistry. 2017(35). 5238–5245. 12 indexed citations
9.
10.
Parrain, Jean‐Luc, et al.. (2013). First studies directed towards the diastereoselective synthesis of the BCD tricyclic core of brownin F. Organic & Biomolecular Chemistry. 11(25). 4178–4178. 13 indexed citations
11.
Comméiras, Laurent, et al.. (2011). Construction of spirolactones with concomitant formation of the fused quaternary centre – application to the synthesis of natural products. Natural Product Reports. 28(4). 763–763. 107 indexed citations
12.
Mathew, Smitha C., Youlet By, A. Berthault, et al.. (2010). Expeditious synthesis and biological evaluation of new C-6 1,2,3-triazole adenosine derivatives A1 receptor antagonists or agonists. Organic & Biomolecular Chemistry. 8(17). 3874–3874. 17 indexed citations
13.
Rahmani, Raphaël, Laurent Comméiras, Gaëlle Chouraqui, et al.. (2009). Copper‐Catalyzed Preparation of γ‐Alkylidenebutenolides and Isocoumarins under Mild Palladium‐Free Conditions. Advanced Synthesis & Catalysis. 351(5). 779–788. 79 indexed citations
14.
Mathew, Smitha C., Nandita Ghosh, Youlet By, et al.. (2009). Design, synthesis and biological evaluation of a bivalent μ opiate and adenosine A1 receptor antagonist. Bioorganic & Medicinal Chemistry Letters. 19(23). 6736–6739. 18 indexed citations
15.
Paterson, Ian, Kate Ashton, Robert Britton, et al.. (2008). Total Synthesis of (−)‐Reidispongiolide A, an Actin‐Targeting Macrolide Isolated from the Marine Sponge Reidispongia coerulea. Chemistry - An Asian Journal. 3(2). 367–387. 33 indexed citations
16.
Paterson, Ian, Kate Ashton, Robert Britton, et al.. (2007). Total Synthesis of (−)‐Reidispongiolide A, an Actin‐Targeting Marine Macrolide. Angewandte Chemie International Edition. 46(32). 6167–6171. 37 indexed citations
17.
Paterson, Ian, Kate Ashton, Robert Britton, et al.. (2007). Total Synthesis of (−)‐Reidispongiolide A, an Actin‐Targeting Marine Macrolide. Angewandte Chemie. 119(32). 6279–6283. 9 indexed citations
18.
Katsonis, Nathalie, et al.. (2003). A Molecular Approach to Self‐Assembly of Trimethylsilylacetylene Derivatives on Gold. Chemistry - A European Journal. 9(11). 2574–2581. 28 indexed citations
19.
Petit, Marc, Gaëlle Chouraqui, Corinne Aubert, & Max Malacrìa. (2003). New and Efficient Procedure for the Preparation of Unsymmetrical Silaketals. Organic Letters. 5(12). 2037–2040. 30 indexed citations
20.
Petit, Marc, Gaëlle Chouraqui, Phannarath Phansavath, Corinne Aubert, & Max Malacrìa. (2002). New Efficient Construction of the ABC Core of the Taxoids via a Sequence of Consecutive Cobalt(I)-Mediated [2 + 2 + 2] and [4 + 2] Cyclizations. Organic Letters. 4(6). 1027–1029. 33 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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