Yves Troin

1.8k total citations
101 papers, 1.5k citations indexed

About

Yves Troin is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, Yves Troin has authored 101 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 79 papers in Organic Chemistry, 26 papers in Molecular Biology and 13 papers in Pharmacology. Recurrent topics in Yves Troin's work include Asymmetric Synthesis and Catalysis (22 papers), Synthetic Organic Chemistry Methods (20 papers) and Chemical synthesis and alkaloids (18 papers). Yves Troin is often cited by papers focused on Asymmetric Synthesis and Catalysis (22 papers), Synthetic Organic Chemistry Methods (20 papers) and Chemical synthesis and alkaloids (18 papers). Yves Troin collaborates with scholars based in France, Morocco and Spain. Yves Troin's co-authors include Anne-Christine Franville, Daniel Zambón, Rachid Mahiou, Jean‐Louis Canet, Jean‐Claude Gramain, Stéphane Ciblat, Jacques Gelas, Pierre Chalard, Gérald Guillaumet and Henri Veschambre and has published in prestigious journals such as SHILAP Revista de lepidopterología, Chemistry of Materials and Journal of Medicinal Chemistry.

In The Last Decade

Yves Troin

98 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yves Troin France 20 935 356 290 153 119 101 1.5k
Gyula Argay Hungary 20 729 0.8× 267 0.8× 391 1.3× 395 2.6× 141 1.2× 101 1.4k
Yuji Tokunaga Japan 21 1.0k 1.1× 295 0.8× 324 1.1× 149 1.0× 357 3.0× 100 1.4k
Wolf‐D. Woggon Switzerland 22 795 0.9× 309 0.9× 576 2.0× 601 3.9× 171 1.4× 56 1.6k
Armen M. Boldi United States 20 1.1k 1.2× 189 0.5× 288 1.0× 98 0.6× 53 0.4× 25 1.4k
Cathy Einhorn France 21 1.1k 1.2× 266 0.7× 294 1.0× 207 1.4× 66 0.6× 43 1.4k
Ryu Yamasaki Japan 25 1.2k 1.3× 197 0.6× 375 1.3× 157 1.0× 157 1.3× 71 1.5k
Subhash P. Chavan India 28 2.0k 2.2× 213 0.6× 719 2.5× 285 1.9× 86 0.7× 167 2.6k
Patrice Capdevielle France 23 984 1.1× 205 0.6× 222 0.8× 374 2.4× 43 0.4× 67 1.4k
B. Waegell France 22 1.3k 1.4× 210 0.6× 274 0.9× 387 2.5× 180 1.5× 128 1.7k
Koreharu Ogata Japan 15 478 0.5× 118 0.3× 200 0.7× 113 0.7× 121 1.0× 48 820

Countries citing papers authored by Yves Troin

Since Specialization
Citations

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

Fields of papers citing papers by Yves Troin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yves Troin

This figure shows the co-authorship network connecting the top 25 collaborators of Yves Troin. A scholar is included among the top collaborators of Yves Troin 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 Yves Troin. Yves Troin 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.
Ricelli, Alessandra, Venturina Stagni, Angela Cirigliano, et al.. (2022). Antifungal and Cytotoxic Activity of Diterpenes and Bisnorsesquiterpenoides from the Latex of Euphorbia resinifera Berg. Molecules. 27(16). 5234–5234. 9 indexed citations
2.
Decombat, Caroline, Laëtitia Delort, Mostafà Khouili, et al.. (2020). Synthesis and Biological Evaluation of New Naphthoquinones Derivatives. Current Organic Synthesis. 17(3). 224–229. 5 indexed citations
3.
Troin, Yves, et al.. (2017). Stereoselective strategies for the construction of polysubstituted piperidinic compounds and their applications in natural products’ synthesis. Organic Chemistry Frontiers. 4(8). 1655–1704. 35 indexed citations
4.
Bourg, Stéphane, Pascal Bonnet, Christiane Guguen‐Guillouzo, et al.. (2016). Novel optimization of valmerins (tetrahydropyrido[1,2-a]isoindolones) as potent dual CDK5/GSK3 inhibitors. European Journal of Medicinal Chemistry. 115. 311–325. 16 indexed citations
5.
Bourg, Stéphane, Pascal Bonnet, Olivier Lozach, et al.. (2015). Advances in tetrahydropyrido[1,2- a ]isoindolone (valmerins) series: Potent glycogen synthase kinase 3 and cyclin dependent kinase 5 inhibitors. European Journal of Medicinal Chemistry. 101. 274–287. 27 indexed citations
6.
Chalard, Pierre, et al.. (2013). Efficient synthesis of β’-amino-α,β-unsaturated ketones. Beilstein Journal of Organic Chemistry. 9. 486–495. 10 indexed citations
7.
Diallo, Drissa, Jean Claude Chalchat, Gilles Figuérédo, et al.. (2011). An ethnobotanical and phytochemical study of the African medicinal plant Guiera senegalensis J. F. Gmel. Journal of Medicinal Plants Research. 5(9). 1639–1651. 27 indexed citations
8.
George, Pascal, et al.. (2011). Synthesis and biological evaluation of analogues of M6G. European Journal of Medicinal Chemistry. 46(9). 4035–4041. 13 indexed citations
9.
Routier, Sylvain, et al.. (2009). New Efficient Route to Fused Aryltetrahydroindolizinones via N‐Acyliminium Intermediates. European Journal of Organic Chemistry. 2009(18). 3011–3021. 13 indexed citations
10.
Troin, Yves, et al.. (2005). A Simple Stereoselective Access to α-Trifluoromethylated Piperidines. Synlett. 1731–1733. 1 indexed citations
11.
Troin, Yves, et al.. (2004). Synthesis of Nitrogen Ligands of C2 Symmetry of the Bis‐piperidyl Type. ChemInform. 35(11). 1 indexed citations
12.
Troin, Yves, et al.. (2003). Synthesis of 4-Substituted Indolizidin-9-one Amino Acid Derivatives. Heterocycles. 60(6). 1447–1447. 5 indexed citations
13.
Ciblat, Stéphane, Jean‐Louis Canet, & Yves Troin. (2001). A new route to 2-spiropiperidines. Tetrahedron Letters. 42(29). 4815–4817. 17 indexed citations
14.
Canet, Jean‐Louis, et al.. (2000). A rapid stereoselective access to highly substituted piperidines. Tetrahedron Letters. 41(50). 9797–9802. 21 indexed citations
15.
Besse, P. Besse-Hoggan Besse-Hoggan Pascale Pascale, Stéphane Ciblat, Jean‐Louis Canet, Yves Troin, & Henri Veschambre. (1999). Stereoselective chemoenzymatic synthesis of both enantiomers of protected 4-amino-2-pentanone. Tetrahedron Asymmetry. 10(11). 2213–2224. 19 indexed citations
16.
Ibrahim‐Ouali, Malika, et al.. (1996). Photochemical synthesis of carbazole derivatives. Synthetic Communications. 26(4). 657–670. 5 indexed citations
17.
18.
Teulade, Jean‐Claude, et al.. (1994). Synthesis of Azacarbazoles. Heterocycles. 38(6). 1241–1241. 9 indexed citations
19.
Gramain, Jean‐Claude, et al.. (1981). A new photochemical spiroannelation method. Access to substituted spirocyclohexanepiperidines. Journal of the Chemical Society Chemical Communications. 832–832. 8 indexed citations
20.
Gramain, Jean‐Claude, Roland Remuson, & Yves Troin. (1979). Photoreduction d'arylcetones par les amides et les lactames: applications synthetiques. Tetrahedron. 35(6). 753–758. 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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