Gérard Coudert

1.2k total citations
61 papers, 941 citations indexed

About

Gérard Coudert is a scholar working on Organic Chemistry, Molecular Biology and Toxicology. According to data from OpenAlex, Gérard Coudert has authored 61 papers receiving a total of 941 indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Organic Chemistry, 22 papers in Molecular Biology and 9 papers in Toxicology. Recurrent topics in Gérard Coudert's work include Synthesis and Biological Evaluation (14 papers), Chemical Synthesis and Analysis (10 papers) and Bioactive Compounds and Antitumor Agents (9 papers). Gérard Coudert is often cited by papers focused on Synthesis and Biological Evaluation (14 papers), Chemical Synthesis and Analysis (10 papers) and Bioactive Compounds and Antitumor Agents (9 papers). Gérard Coudert collaborates with scholars based in France, Morocco and Poland. Gérard Coudert's co-authors include Jean‐Yves Mérour, Gérald Guillaumet, Pascal Bouyssou, Isabelle Gillaizeau, Sylvain Routier, Sylvain Routier, Bernard Loubinoux, Valérie Bénéteau, Ulrich Jacquemard and Alain St. Pierre and has published in prestigious journals such as Journal of Medicinal Chemistry, The Journal of Organic Chemistry and Tetrahedron.

In The Last Decade

Gérard Coudert

60 papers receiving 908 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gérard Coudert France 18 780 309 76 70 58 61 941
Helena M. C. Ferraz Brazil 19 858 1.1× 173 0.6× 64 0.8× 47 0.7× 76 1.3× 72 1.0k
Sivappa Rasapalli United States 19 792 1.0× 231 0.7× 97 1.3× 52 0.7× 23 0.4× 49 925
Yasuyoshi Miki Japan 18 763 1.0× 263 0.9× 98 1.3× 53 0.8× 62 1.1× 102 1.0k
Steven R. Angle United States 23 1.1k 1.4× 255 0.8× 88 1.2× 75 1.1× 43 0.7× 59 1.3k
Luca Parlanti Italy 10 805 1.0× 215 0.7× 89 1.2× 39 0.6× 31 0.5× 18 925
Hidetsura Cho Japan 16 971 1.2× 376 1.2× 105 1.4× 24 0.3× 64 1.1× 54 1.2k
Matthew J. Sharp United States 23 1.3k 1.7× 197 0.6× 96 1.3× 30 0.4× 46 0.8× 35 1.5k
Tomasz Janosik Sweden 17 590 0.8× 249 0.8× 56 0.7× 86 1.2× 25 0.4× 44 837
Tameo Iwasaki Japan 20 821 1.1× 567 1.8× 84 1.1× 25 0.4× 78 1.3× 82 1.2k
Francisco Yuste Mexico 17 658 0.8× 194 0.6× 70 0.9× 24 0.3× 73 1.3× 64 851

Countries citing papers authored by Gérard Coudert

Since Specialization
Citations

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

Fields of papers citing papers by Gérard Coudert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gérard Coudert

This figure shows the co-authorship network connecting the top 25 collaborators of Gérard Coudert. A scholar is included among the top collaborators of Gérard Coudert 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 Gérard Coudert. Gérard Coudert 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.
Bouissane, Latifa, Mostafà Khouili, Gérard Coudert, María Dolors Pujol, & Gérald Guillaumet. (2023). New and promising type of leukotriene B4 (LTB4) antagonists based on the 1,4-benzodioxine structure. European Journal of Medicinal Chemistry. 254. 115332–115332. 4 indexed citations
2.
Routier, Sylvain, et al.. (2010). Synthesis and biological evaluation of novel benzodioxinocarbazoles (BDCZs) as potential anticancer agents. Bioorganic & Medicinal Chemistry Letters. 20(15). 4670–4674. 5 indexed citations
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Gillaizeau, Isabelle, et al.. (2009). Nucleophilic Addition onto Methyl-4H-1,4-oxazine-3-carboxylate Moiety: Short Access to 1,4-Diazine Privileged Substructures. The Journal of Organic Chemistry. 74(7). 2911–2914. 9 indexed citations
7.
Coudert, Gérard, Sylvain Routier, Bruno Pfeiffer, et al.. (2008). Novel 5-azaindolocarbazoles as cytotoxic agents and Chk1 inhibitors. Bioorganic & Medicinal Chemistry. 16(9). 5303–5321. 28 indexed citations
8.
Gillaizeau, Isabelle, et al.. (2007). Easy Access to New Heterocyclic Systems:  1,4-Oxazine and Substituted 1,4-Oxazines. The Journal of Organic Chemistry. 72(13). 4832–4836. 33 indexed citations
9.
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Jacquemard, Ulrich, et al.. (2004). Mild and selective deprotection of carbamates with Bu4NF. Tetrahedron. 60(44). 10039–10047. 107 indexed citations
11.
Arimondo, Paola B., Brigitte Baldeyrou, William Laine, et al.. (2001). DNA interaction and cytotoxicity of a new series of indolo[2,3-b]quinoxaline and pyridopyrazino[2,3-b]indole derivatives. Chemico-Biological Interactions. 138(1). 59–75. 22 indexed citations
12.
Thiéry, Valérie, Gérard Coudert, Luc Morin‐Allory, & Gérald Guillaumet. (1995). Convenient synthesis of 2-substituted-6 or 7-acylated-1,4-benzodioxin or 2,3-dihydro-1,4-benzodioxin derivatives. Tetrahedron. 51(9). 2619–2628. 10 indexed citations
13.
Csı́k, Gabriella, Simone Averbeck, D. Averbeck, et al.. (1994). Biophysical and biological properties of newly synthesized dioxinocoumarin derivatives. Journal of Photochemistry and Photobiology B Biology. 24(2). 129–139. 6 indexed citations
14.
Khouili, Mostafà, Saïd Lazar, Gérald Guillaumet, & Gérard Coudert. (1994). Synthesis of enantiomerically pure 7-hydroxy-2-substituted-2,3-dihydro-1,4-benzodioxin derivatives. Tetrahedron Asymmetry. 5(4). 535–536. 5 indexed citations
15.
Besson, Thierry, et al.. (1993). Convenient synthesis of 5-substituted-6-methoxy or 6-hydroxy-2,3-dihydro-1,4-benzodioxins via lithiated intermediates. Tetrahedron. 49(7). 1421–1430. 4 indexed citations
16.
Csı́k, Gabriella, et al.. (1993). Biophysical and biological properties of newly synthesized dioxinocoumarin derivatives.. Journal of Photochemistry and Photobiology B Biology. 19(2). 119–124. 5 indexed citations
17.
Guillaumet, Gérald, et al.. (1990). Synthèse et propriétés biologiques photoinduites de dioxinnocoumarines linéaires. European Journal of Medicinal Chemistry. 25(1). 45–51. 13 indexed citations
18.
Coudert, Gérard, et al.. (1986). A Novel, Unequivocal Synthesis of Polyethylene Glycols. Synthetic Communications. 16(1). 19–26. 29 indexed citations
19.
Guillaumet, Gérald, Gérard Coudert, & Bernard Loubinoux. (1983). 2H‐1,5‐Benzodioxepin and 3‐Halo Derivatives. Angewandte Chemie International Edition in English. 22(1). 64–65. 6 indexed citations
20.
Guillaumet, Gérald, Gérard Coudert, & Bernard Loubinoux. (1983). 2H‐1,5‐Benzodioxepin und 3‐Halogen‐Derivate. Angewandte Chemie. 95(1). 50–51. 2 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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