Luc Dechoux

791 total citations
54 papers, 556 citations indexed

About

Luc Dechoux is a scholar working on Organic Chemistry, Molecular Biology and Pharmaceutical Science. According to data from OpenAlex, Luc Dechoux has authored 54 papers receiving a total of 556 indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Organic Chemistry, 12 papers in Molecular Biology and 5 papers in Pharmaceutical Science. Recurrent topics in Luc Dechoux's work include Asymmetric Synthesis and Catalysis (22 papers), Synthetic Organic Chemistry Methods (21 papers) and Cyclopropane Reaction Mechanisms (15 papers). Luc Dechoux is often cited by papers focused on Asymmetric Synthesis and Catalysis (22 papers), Synthetic Organic Chemistry Methods (21 papers) and Cyclopropane Reaction Mechanisms (15 papers). Luc Dechoux collaborates with scholars based in France, China and Slovakia. Luc Dechoux's co-authors include Eric Doris, Claude Agami, Charles Mioskowski, Serge Thorimbert, Liang Chang, Cécilia Ménard‐Moyon, Mohand Melaïmi, Matthieu Sollogoub, Louis Jung and Yongmin Zhang and has published in prestigious journals such as The Lancet, Journal of the American Chemical Society and Chemical Communications.

In The Last Decade

Luc Dechoux

54 papers receiving 529 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Luc Dechoux France 14 451 130 51 44 26 54 556
Frank J. Urban United States 13 304 0.7× 247 1.9× 17 0.3× 30 0.7× 22 0.8× 33 452
S. Malla Reddy India 11 288 0.6× 108 0.8× 32 0.6× 32 0.7× 8 0.3× 15 403
Hui‐Chang Lin Taiwan 16 462 1.0× 222 1.7× 19 0.4× 25 0.6× 87 3.3× 39 594
Balbino Mancheño Spain 12 308 0.7× 90 0.7× 40 0.8× 29 0.7× 16 0.6× 24 389
Margarita Brovetto Uruguay 10 237 0.5× 229 1.8× 21 0.4× 47 1.1× 15 0.6× 23 395
S. Hanessian Canada 11 429 1.0× 194 1.5× 22 0.4× 27 0.6× 30 1.2× 24 498
Silvana Pedatella Italy 15 423 0.9× 249 1.9× 9 0.2× 45 1.0× 28 1.1× 62 548
Andrew M. Camelio United States 9 237 0.5× 105 0.8× 16 0.3× 36 0.8× 7 0.3× 11 345
Mohamed Takhi India 15 584 1.3× 350 2.7× 32 0.6× 62 1.4× 7 0.3× 30 689
László Juhász Hungary 11 247 0.5× 217 1.7× 70 1.4× 7 0.2× 10 0.4× 31 404

Countries citing papers authored by Luc Dechoux

Since Specialization
Citations

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

Fields of papers citing papers by Luc Dechoux

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Luc Dechoux

This figure shows the co-authorship network connecting the top 25 collaborators of Luc Dechoux. A scholar is included among the top collaborators of Luc Dechoux 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 Luc Dechoux. Luc Dechoux 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.
Chang, Liang, et al.. (2022). Iron Catalyzed Dearomatization of Pyridines into Annelated Azepine Derivatives in a One-Step, Three-Component Reaction. Organic Letters. 25(1). 256–260. 6 indexed citations
2.
Chang, Liang, Nathalie Fischer‐Durand, Geoffrey Gontard, et al.. (2021). A Solvent‐free, Catalyst‐free Formal [3+3] Cycloaddition Dearomatization Strategy: Towards New Fluorophores for Biomolecules Labelling. ChemSusChem. 14(8). 1821–1824. 5 indexed citations
3.
Chang, Liang, Serge Thorimbert, & Luc Dechoux. (2019). The bio-based methyl coumalate involved Morita–Baylis–Hillman reaction. Organic & Biomolecular Chemistry. 17(10). 2784–2791. 12 indexed citations
4.
Chang, Liang, Nadja Klipfel, Luc Dechoux, & Serge Thorimbert. (2018). A solvent-free, base-catalyzed domino reaction towards trifluoromethylated benzenes from bio-based methyl coumalate. Green Chemistry. 20(7). 1491–1498. 13 indexed citations
5.
Wu, Shaoping, Lili Yang, Wenji Sun, et al.. (2017). Design, synthesis and biological evaluation of gentiopicroside derivatives as potential antiviral inhibitors. European Journal of Medicinal Chemistry. 130. 308–319. 28 indexed citations
6.
Chang, Liang, et al.. (2017). Preparation of Substituted 2H-Pyrans via a Cascade Reaction from Methyl Coumalate and Activated Methylene Nucleophiles. The Journal of Organic Chemistry. 82(10). 5499–5505. 17 indexed citations
7.
Wu, Shaoping, Ying‐Yong Zhao, Serge Thorimbert, et al.. (2016). Research Progress of Natural Product Gentiopicroside - a Secoiridoid Compound. Mini-Reviews in Medicinal Chemistry. 17(1). 62–77. 42 indexed citations
8.
Wu, Shaoping, Yongmin Zhang, Jyoti Agarwal, et al.. (2015). Studies towards the synthesis of secoiridoids. Tetrahedron. 71(40). 7663–7669. 6 indexed citations
9.
Agami, Claude, et al.. (2003). Synthesis of new enantiomerically pure α,β-unsaturated bicyclic lactams. Tetrahedron Letters. 44(41). 7667–7669. 7 indexed citations
10.
Dechoux, Luc, et al.. (2002). An Efficient Synthesis of Polysubstituted 3-Halo-2(1H)-Pyridinones. Synthesis. 2002(1). 2 indexed citations
11.
Agami, Claude, Luc Dechoux, & Mohand Melaïmi. (2000). An Efficient Synthesis of Pyrimidines from β-Amino Alcohols. Organic Letters. 2(5). 633–634. 6 indexed citations
12.
Agami, Claude, et al.. (1999). A New Chiral Auxiliary Derived from (2S)-Phenylglycinol: an Access to Enantiomerically Pure β-Amino Acids. Synlett. 1999(6). 727–728. 8 indexed citations
13.
Dechoux, Luc, et al.. (1999). Studies Directed Toward the Synthesis of Taxanes: Construction of the Tricyclo[5.3.1.01,7]undecane System. European Journal of Organic Chemistry. 1999(12). 3251–3256. 8 indexed citations
14.
Agami, Claude, et al.. (1998). Synthesis of enantiopure substituted aziridines by diastereoselective N-bromocyclization and nucleophile-mediated regioselective opening. Tetrahedron Letters. 39(30). 5373–5374. 6 indexed citations
15.
Ingenbleek, Yves, et al.. (1997). Iodised rapeseed oil for eradication of severe endemic goitre. The Lancet. 350(9090). 1542–1545. 16 indexed citations
16.
Dechoux, Luc, Eric Doris, & Charles Mioskowski. (1996). Regiospecific access to cyclic allylic alcohols by reductive alkylation of α-alkyloxy-epoxides. Chemical Communications. 549–550. 11 indexed citations
17.
Dechoux, Luc, et al.. (1995). Tandem Addition-Bromofunctionalization of γ,δ-Unsaturated Grignard Reagents to Benzonitriles. Synthesis. 1995(3). 242–244. 3 indexed citations
18.
Doris, Eric, Luc Dechoux, & Charles Mioskowski. (1995). Reaction of cyclic .alpha.-hydroxy epoxides with a strong base: a new 1,2-rearrangement, evidence for a carbenoid pathway.. Journal of the American Chemical Society. 117(51). 12700–12704. 31 indexed citations
19.
Dechoux, Luc & Eric Doris. (1994). Acidic isomerization of vicinally substituted (cis)-acceptor-donor cyclopropanes via an open ring mechanism. Tetrahedron Letters. 35(13). 2017–2020. 11 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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