Vincent Reboul

872 total citations
37 papers, 661 citations indexed

About

Vincent Reboul is a scholar working on Organic Chemistry, Molecular Biology and Spectroscopy. According to data from OpenAlex, Vincent Reboul has authored 37 papers receiving a total of 661 indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Organic Chemistry, 8 papers in Molecular Biology and 3 papers in Spectroscopy. Recurrent topics in Vincent Reboul's work include Synthesis and Catalytic Reactions (11 papers), Sulfur-Based Synthesis Techniques (8 papers) and Chemical Synthesis and Reactions (7 papers). Vincent Reboul is often cited by papers focused on Synthesis and Catalytic Reactions (11 papers), Sulfur-Based Synthesis Techniques (8 papers) and Chemical Synthesis and Reactions (7 papers). Vincent Reboul collaborates with scholars based in France, United States and Switzerland. Vincent Reboul's co-authors include Patrick Metzner, Jean‐François Lohier, Hamid Marzag, Annie−Claude Gaumont, Cédric Spitz, Virginie Blot, Xavier Franck, Nelly Plé, Johannes F. P. Colell and Alain Turck and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Chemical Communications.

In The Last Decade

Vincent Reboul

37 papers receiving 656 citations

Peers

Vincent Reboul

SPECT

Martin Westermaier Germany

Utpal Das India

Germana Mazzanti Italy

Isabel Merino Spain

Madhu Ganesh India

Gagik G. Melikyan United States

Josefa Flórez Spain

Brian P. Woods United States

Olesya V. Khoroshilova Russia

Ryoji Fujiyama Japan

Martin Westermaier Germany

Vincent Reboul

468 ×0.8

81 ×0.9

49 ×0.7

47 ×0.8

SPECT

31 ×0.9

Citations per year, relative to Vincent Reboul Vincent Reboul (= 1×) peers Martin Westermaier

Countries citing papers authored by Vincent Reboul

Since Specialization

Citations

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

Fields of papers citing papers by Vincent Reboul

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vincent Reboul

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

All Works

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20 of 20 papers shown

Tournier, Benjamin B., Audrey Davis, Emmanuelle Dubost⧫, et al.. (2020). Design of iodinated radioligands for SPECT imaging of central human 5-HT4R using a ligand lipophilicity efficiency approach. Bioorganic Chemistry. 96. 103582–103582. 2 indexed citations

Reboul, Vincent, et al.. (2020). A Straightforward Synthesis of N-Substituted Ureas from Primary Amides. Synthesis. 52(14). 2099–2105. 13 indexed citations

Marzag, Hamid, Johannes F. P. Colell, Guannan Zhang, et al.. (2019). Iodonitrene in Action: Direct Transformation of Amino Acids into Terminal Diazirines and ¹⁵N₂-Diazirines and Their Application as Hyperpolarized Markers. Journal of the American Chemical Society. 141(34). 13689–13696. 43 indexed citations

Zhang, Guannan, et al.. (2019). Terminal Diazirines Enable Reverse Polarization Transfer from ¹⁵N₂ Singlets. Angewandte Chemie International Edition. 58(32). 11118–11124. 14 indexed citations

Zhang, Guannan, et al.. (2019). Terminal Diazirines Enable Reverse Polarization Transfer from ¹⁵N₂ Singlets. Angewandte Chemie. 131(32). 11235–11241. 7 indexed citations

Lohier, Jean‐François, Anne‐Laure Barthelemy, Elsa Anselmi, et al.. (2018). One‐Pot Synthesis of Aryl‐ and Alkyl S‐Perfluoroalkylated NH‐Sulfoximines from Sulfides. Chemistry - A European Journal. 24(64). 17006–17010. 45 indexed citations

Lohier, Jean‐François, et al.. (2017). Mechanistic investigation of the NH-sulfoximination of sulfide. Evidence for λ⁶-sulfanenitrile intermediates. Chemical Communications. 53(12). 2064–2067. 88 indexed citations

Marzag, Hamid, Marie Schuler, Arnaud Tatibouët, & Vincent Reboul. (2016). Synthesis of Methionine‐Derived Endocyclic Sulfilimines and Sulfoximines. European Journal of Organic Chemistry. 2017(4). 896–900. 17 indexed citations

Lohier, Jean‐François, et al.. (2013). Asymmetric Three-Component Domino Reaction: An Original Access to Chiral Nonracemic 1,3-Thiazin-2-ones. Organic Letters. 15(22). 5710–5713. 12 indexed citations

10.

Legay, Rémi, et al.. (2012). Facile access to γ-aminothiols from 1,3-thiazines via a microwave-assisted three-component reaction. Tetrahedron. 68(44). 9016–9022. 11 indexed citations

11.

Spitz, Cédric, Vincent Reboul, & Patrick Metzner. (2011). Cyclic sulfenamide: versatile template for the synthesis of 1,4-benzothiazepines. Tetrahedron Letters. 52(48). 6321–6324. 14 indexed citations

12.

Lohier, Jean‐François, et al.. (2007). A straightforward asymmetric synthesis of 1,2-disubstituted ferrocenylalkyl amines with the unusual (SFc,S) configuration. Chemical Communications. 4875–4875. 10 indexed citations

13.

Blot, Virginie, et al.. (2005). Developments of Asymmetric Synthesis Mediated by Chiral Sulfur Reagents. Phosphorus, sulfur, and silicon and the related elements. 180(5-6). 1171–1182. 10 indexed citations

14.

Reboul, Vincent, et al.. (2004). Catalytic ferrocenyl sulfides for the asymmetric transformation of aldehydes into epoxides. Tetrahedron Asymmetry. 15(20). 3275–3280. 20 indexed citations

15.

Reboul, Vincent, et al.. (2004). First Epoxidation Reaction of Carbonyl Compounds via Ferrocenyl Sulfur Ylides.. ChemInform. 35(7). 1 indexed citations

16.

Mojovic, Ljubica, Alain Turck, Nelly Plé, et al.. (2004). Syntheses of sulfoxide derivatives in the benzodiazine series. Diazines. Part 37. Tetrahedron. 60(36). 7983–7994. 8 indexed citations

17.

Reboul, Vincent, et al.. (2003). Atroposelectivity of Reactions of Benzylic Metalated Thiobenzamides and Thionaphthamides. European Journal of Organic Chemistry. 2003(17). 3398–3406. 10 indexed citations

18.

Dantale, Shubhada W., Vincent Reboul, Patrick Metzner, & Christian Philouze. (2002). First Use of Axially Chiral Thioamides for the Stereocontrol of C−C Bond Formation. Chemistry - A European Journal. 8(3). 632–640. 29 indexed citations

19.

Reboul, Vincent, Catherine Guillou, & Claude Thal. (1999). Synthesis of 4-substituted-tricarbonyl(η4-cyclohexa-2,4-dien-1-one)iron complexes. Tetrahedron Letters. 40(48). 8355–8358. 3 indexed citations

20.

Guillou, Catherine, Nicolas Millot, Vincent Reboul, & Claude Thal. (1996). Synthesis of cationic 1-substituted-dicarbonyl(η5-4-methoxycyclohexadienyl)-(triphenylphosphine)iron complexes. Tetrahedron Letters. 37(26). 4515–4518. 8 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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