Gilles Dujardin

2.1k total citations
71 papers, 1.2k citations indexed

About

Gilles Dujardin is a scholar working on Organic Chemistry, Molecular Biology and Pharmaceutical Science. According to data from OpenAlex, Gilles Dujardin has authored 71 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 65 papers in Organic Chemistry, 30 papers in Molecular Biology and 10 papers in Pharmaceutical Science. Recurrent topics in Gilles Dujardin's work include Asymmetric Synthesis and Catalysis (32 papers), Carbohydrate Chemistry and Synthesis (26 papers) and Chemical Synthesis and Analysis (24 papers). Gilles Dujardin is often cited by papers focused on Asymmetric Synthesis and Catalysis (32 papers), Carbohydrate Chemistry and Synthesis (26 papers) and Chemical Synthesis and Analysis (24 papers). Gilles Dujardin collaborates with scholars based in France, Tunisia and Egypt. Gilles Dujardin's co-authors include Arnaud Martel, Robert Dhal, Jean Martínez, Isabelle Parrot, Thanh Bình Nguyễn, Eric Brown, Mathieu Y. Laurent, V. Maisonneuve, Pascal Gosselin and Sylvain Collet and has published in prestigious journals such as Chemical Reviews, Angewandte Chemie International Edition and Journal of Medicinal Chemistry.

In The Last Decade

Gilles Dujardin

70 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
Gilles Dujardin France 20 1.1k 327 122 93 66 71 1.2k
Joseph Cs. Jászberényi United States 24 1.3k 1.2× 276 0.8× 94 0.8× 112 1.2× 68 1.0× 58 1.4k
Stephanie Meyer Germany 11 694 0.6× 186 0.6× 159 1.3× 125 1.3× 88 1.3× 14 819
Gilbert Revıal France 21 1.1k 1.0× 327 1.0× 54 0.4× 123 1.3× 107 1.6× 56 1.3k
François Trécourt France 27 1.5k 1.4× 242 0.7× 111 0.9× 228 2.5× 80 1.2× 52 1.7k
Leticia Quintero Mexico 21 1.3k 1.2× 358 1.1× 64 0.5× 212 2.3× 71 1.1× 96 1.5k
Sandrine Py France 22 1.1k 1.1× 368 1.1× 124 1.0× 148 1.6× 36 0.5× 52 1.2k
Akhilesh K. Verma India 5 1.0k 1.0× 235 0.7× 89 0.7× 155 1.7× 66 1.0× 14 1.3k
Ana M. Martı́n Castro Spain 17 1.3k 1.2× 235 0.7× 67 0.5× 211 2.3× 76 1.2× 39 1.4k
Giovanni W. Amarante Brazil 21 1.3k 1.2× 326 1.0× 172 1.4× 163 1.8× 58 0.9× 86 1.5k

Countries citing papers authored by Gilles Dujardin

Since Specialization
Citations

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

Fields of papers citing papers by Gilles Dujardin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gilles Dujardin

This figure shows the co-authorship network connecting the top 25 collaborators of Gilles Dujardin. A scholar is included among the top collaborators of Gilles Dujardin 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 Gilles Dujardin. Gilles Dujardin 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.
Tessier, Arnaud, Muriel Pipelier, Gilles Dujardin, et al.. (2020). Synthesis of Constrained C‐Glycosyl Amino Acid Derivatives Involving 1,3‐Dipolar Cycloaddition of Cyclic Nitrone as Key Step. European Journal of Organic Chemistry. 2020(43). 6749–6757. 2 indexed citations
2.
Chany, Anne‐Caroline, Monique Mathé‐Allainmat, Jacques Lebreton, et al.. (2019). Function-Oriented Synthesis toward Peloruside A Analogues. Organic Letters. 21(9). 2988–2992. 4 indexed citations
3.
Lebreton, Jacques, Gilles Dujardin, Sylvain Collet, et al.. (2018). Stereodivergent approach in the protected glycal synthesis of L-vancosamine, L-saccharosamine, L-daunosamine and L-ristosamine involving a ring-closing metathesis step. Beilstein Journal of Organic Chemistry. 14. 2949–2955. 7 indexed citations
4.
Guillarme, Stéphane, Arnaud Martel, Jacques Lebreton, et al.. (2018). Stereospecific C‐Glycosylation by Mizoroki–Heck Reaction: A Powerful and Easy‐to‐Set‐Up Synthetic Tool to Access α‐ and β‐Aryl‐C‐Glycosides. Chemistry - A European Journal. 24(53). 14069–14074. 20 indexed citations
5.
Nourry, Arnaud, et al.. (2018). Addition of Organozinc Reagents to Glycopyranosyl Cyanides: Access to Keto Ester‐C‐glycosides or Unsaturated Acyl‐C‐glycosides. European Journal of Organic Chemistry. 2018(14). 1735–1738. 8 indexed citations
6.
Chany, Anne‐Caroline, et al.. (2017). Advances in the TBAF-induced aldol-type addition of α-trialkylsilyl-α-diazoacetones: TIPS versus TES. Comptes Rendus Chimie. 20(6). 595–600. 2 indexed citations
7.
Hamdi, Abdelrahman, et al.. (2016). Acetylene-free synthesis of vinyloxy pyridine and quinoline. Tetrahedron Letters. 57(51). 5825–5829. 5 indexed citations
8.
Dujardin, Gilles, et al.. (2015). MgI2‐Mediated Chemoselective Cleavage of Protecting Groups: An Alternative to Conventional Deprotection Methodologies. Chemistry - A European Journal. 21(31). 11014–11016. 11 indexed citations
9.
Zimmermann, Nicolas, Bertrand Carboni, Pascal Gosselin, et al.. (2013). Convergent Strategy Towards the Synthesis of Restricted Analogues of Peloruside A. European Journal of Organic Chemistry. 2013(12). 2303–2315. 13 indexed citations
10.
11.
Nguyễn, Thanh Bình, et al.. (2010). 1,3-Dipolar Cycloadditions of Nitrones to Heterosubstituted Alkenes. Part 1: Oxa and Aza-substituted Alkenes. Organic Preparations and Procedures International. 42(5). 387–431. 33 indexed citations
12.
Ibanez, Sébastien, Gilles Dujardin, & Laurence Després. (2009). Stability of floral specialization in Trollius europaeus in contrasting ecological environments. Journal of Evolutionary Biology. 22(6). 1183–1192. 10 indexed citations
13.
Tardy, Sébastien, et al.. (2008). Carbohydrate-Based Spiro-1,3-oxazolidine-2-thiones: Stereoselective Approaches Using Aziridines and Epoxides. HAL (Le Centre pour la Communication Scientifique Directe). 1 indexed citations
14.
Nguyễn, Thanh Bình, Arnaud Martel, Robert Dhal, & Gilles Dujardin. (2008). 1,3-Dipolar Cycloaddition of N-Substituted Dipolarophiles and Nitrones:  Highly Efficient Solvent-Free Reaction. The Journal of Organic Chemistry. 73(7). 2621–2632. 32 indexed citations
15.
Dujardin, Gilles, et al.. (2008). Glycosidations of 2-deoxy glycosyl dithiophosphates using a tagged iodine(iii)-promoter for simple purification. Organic & Biomolecular Chemistry. 6(5). 893–893. 8 indexed citations
16.
Dhal, Robert, et al.. (2004). Preparation of Chiral N‐Vinyl Oxazolidinones by a Simple General Procedure.. ChemInform. 35(7). 2 indexed citations
17.
Dhal, Robert, et al.. (2000). First Asymmetric Synthesis of a 6-Alkoxy-5,6-dihydro-1,3-oxazine:  A Promising Enantioselective Route to β-Amido Aldehydes. Organic Letters. 2(5). 585–588. 29 indexed citations
18.
Michelet, Véronique, Jean‐Pierre Genêt, & Gilles Dujardin. (1997). A Pd(0)-catalyzed route to functionalized β-C-glycosides from β-C-glycosylaldehydes. Tetrahedron Letters. 38(44). 7741–7744. 4 indexed citations
19.
Dujardin, Gilles, et al.. (1996). Chiral enol ethers in carbohydrate chemistry: De novo synthesis of protected L-2-deoxy hexoses. Tetrahedron Letters. 37(23). 4007–4010. 20 indexed citations
20.
Hayes, Patricia Y., Gilles Dujardin, & Christian Maignan. (1996). (S)-(+)-3-p-Tolylsulfinylbut-3-en-2-one: A spectacular oxabutadiene for asymmetric cycloaddition of styrenic compounds. Tetrahedron Letters. 37(21). 3687–3690. 17 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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