Odile Ruel

1.4k total citations
22 papers, 1.2k citations indexed

About

Odile Ruel is a scholar working on Organic Chemistry, Materials Chemistry and Biomedical Engineering. According to data from OpenAlex, Odile Ruel has authored 22 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Organic Chemistry, 5 papers in Materials Chemistry and 4 papers in Biomedical Engineering. Recurrent topics in Odile Ruel's work include Synthesis of heterocyclic compounds (6 papers), Synthesis and Reactivity of Sulfur-Containing Compounds (6 papers) and Coordination Chemistry and Organometallics (6 papers). Odile Ruel is often cited by papers focused on Synthesis of heterocyclic compounds (6 papers), Synthesis and Reactivity of Sulfur-Containing Compounds (6 papers) and Coordination Chemistry and Organometallics (6 papers). Odile Ruel collaborates with scholars based in France. Odile Ruel's co-authors include Jean‐Bernard Baudin, S. A. JULIA, Ludovic Jullien, J.‐B. BAUDIN, Georges Hareau, Jean‐François Allemand, Isabelle Aujard, Pierre Neveu, Sandrine Charier and Damien Alcor and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and The Journal of Physical Chemistry B.

In The Last Decade

Odile Ruel

22 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Odile Ruel France 12 592 581 207 201 179 22 1.2k
Thomas P. Brady United States 13 285 0.5× 429 0.7× 234 1.1× 85 0.4× 349 1.9× 19 958
Gopa B. Behera India 6 410 0.7× 799 1.4× 296 1.4× 255 1.3× 356 2.0× 7 1.5k
Gertz I. Likhtenshtein Israel 18 299 0.5× 439 0.8× 216 1.0× 60 0.3× 141 0.8× 61 1.0k
Michiko Iwamura Japan 20 730 1.2× 538 0.9× 357 1.7× 80 0.4× 99 0.6× 60 1.3k
David W. Conrad United States 14 315 0.5× 347 0.6× 499 2.4× 162 0.8× 76 0.4× 20 1.5k
Mark V. Reddington United Kingdom 17 1.4k 2.4× 881 1.5× 357 1.7× 132 0.7× 751 4.2× 17 1.9k
Darryl W. Brousmiche United States 16 298 0.5× 485 0.8× 294 1.4× 171 0.9× 191 1.1× 20 987
Walter M. Müller Germany 23 906 1.5× 512 0.9× 408 2.0× 102 0.5× 513 2.9× 59 1.4k
Michael Pätzel Germany 22 929 1.6× 887 1.5× 260 1.3× 109 0.5× 76 0.4× 64 1.9k
Heiner Detert Germany 21 782 1.3× 705 1.2× 198 1.0× 197 1.0× 148 0.8× 140 1.6k

Countries citing papers authored by Odile Ruel

Since Specialization
Citations

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

Fields of papers citing papers by Odile Ruel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Odile Ruel

This figure shows the co-authorship network connecting the top 25 collaborators of Odile Ruel. A scholar is included among the top collaborators of Odile Ruel 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 Odile Ruel. Odile Ruel 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.
Aujard, Isabelle, et al.. (2006). o‐Nitrobenzyl Photolabile Protecting Groups with Red‐Shifted Absorption: Syntheses and Uncaging Cross‐Sections for One‐ and Two‐Photon Excitation. Chemistry - A European Journal. 12(26). 6865–6879. 264 indexed citations
2.
Charier, Sandrine, Odile Ruel, Jean‐Bernard Baudin, et al.. (2005). Photophysics of a Series of Efficient Fluorescent pH Probes for Dual‐Emission‐Wavelength Measurements in Aqueous Solutions. Chemistry - A European Journal. 12(4). 1097–1113. 46 indexed citations
3.
Charier, Sandrine, Odile Ruel, Jean‐Bernard Baudin, et al.. (2004). An Efficient Fluorescent Probe for Ratiometric pH Measurements in Aqueous Solutions. Angewandte Chemie International Edition. 43(36). 4785–4788. 142 indexed citations
4.
Allemand, Jean‐François, Odile Ruel, Jean‐Bernard Baudin, et al.. (2004). Diaroyl(methanato)boron Difluoride Compounds as Medium‐Sensitive Two‐Photon Fluorescent Probes. Chemistry - A European Journal. 10(6). 1445–1455. 188 indexed citations
5.
Charier, Sandrine, Odile Ruel, Jean‐Bernard Baudin, et al.. (2004). An Efficient Fluorescent Probe for Ratiometric pH Measurements in Aqueous Solutions. Angewandte Chemie. 116(36). 4889–4892. 22 indexed citations
6.
Jullien, Ludovic, A. Lemarchand, Sandrine Charier, Odile Ruel, & J.‐B. BAUDIN. (2003). Two-Site Molecules as a Road for Engineering Complexity in Chemical Systems. The Journal of Physical Chemistry B. 107(36). 9905–9917. 13 indexed citations
7.
Aujard, Isabelle, Jean‐Pierre Baltaze, Jean‐Bernard Baudin, et al.. (2001). Tetrahedral Onsager Crosses for Solubility Improvement and Crystallization Bypass. Journal of the American Chemical Society. 123(34). 8177–8188. 54 indexed citations
8.
Blanchard‐Desce, Mireille, Jean‐Bernard Baudin, Ludovic Jullien, et al.. (1999). Towards highly efficient nonlinear optical chromophores: molecular engineering of octupolar molecules. Optical Materials. 12(2-3). 333–338. 30 indexed citations
9.
Blanchard‐Desce, Mireille, Jean‐Bernard Baudin, Odile Ruel, et al.. (1998). New non-dipolar structures with significant quadratic hyperpoiarizabilites. Optical Materials. 9(1-4). 276–279. 16 indexed citations
10.
BAUDIN, J.‐B., et al.. (1993). Stereochemistry of direct olefin formation from carbonyl compounds and lithiated heterocyclic sulfones. 130(6). 856–878. 2 indexed citations
12.
BAUDIN, J.‐B., Georges Hareau, S. A. JULIA, & Odile Ruel. (1991). A direct synthesis of olefins by reaction of carbonyl compounds with lithio derivatives of 2-[alkyl- or (2′-alkenyl)- or benzyl-sulfonyl]-benzothiazoles.. Tetrahedron Letters. 32(9). 1175–1178. 338 indexed citations
13.
Baudin, Jean‐Bernard, S. A. JULIA, Odile Ruel, & Yuan Wang. (1990). Unusual lithiation of 4-(1′,2′-alkadienesulphinyl)-morpholines. Preparation of substituted propargylic sulphinamides and their hydrolytic desulphinylation into the corresponding allenes. Tetrahedron Letters. 31(2). 213–216. 6 indexed citations
14.
Ruel, Odile, Jean‐Bernard Baudin, & S. A. JULIA. (1990). Preparation and Thermal Properties of N-Alkylidene-Ethenesulfenamides. Synthetic Communications. 20(14). 2151–2164. 5 indexed citations
15.
BAUDIN, J.‐B., et al.. (1985). Thermal Rearrangements ofN-Aryl-1-alkynesulphenamides into Indoline-2-thiones. Synthesis. 1985(10). 956–958. 8 indexed citations
18.
Réglier, Marius, et al.. (1983). Preparation of Pure Alkyl or Phenyl 3-Methyl-1 (EorZ),3- butadienyl Sulphides. Synthesis. 1983(8). 624–628. 5 indexed citations
19.
Ruel, Odile, Bernard Cazes, & S. A. JULIA. (1980). Reaction of 1, 1-Bis(Methylthio)-3-Methyl-1, 3-Butadiene with Lithiated 3-Methyl-2-Butenyl Phenyl Sulfide. A Special Case of Cyclopropane Formation. Synthetic Communications. 10(10). 743–750. 3 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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