Philippe Compain

4.1k total citations
111 papers, 3.5k citations indexed

About

Philippe Compain is a scholar working on Organic Chemistry, Molecular Biology and Physiology. According to data from OpenAlex, Philippe Compain has authored 111 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 107 papers in Organic Chemistry, 66 papers in Molecular Biology and 15 papers in Physiology. Recurrent topics in Philippe Compain's work include Carbohydrate Chemistry and Synthesis (68 papers), Glycosylation and Glycoproteins Research (36 papers) and Synthesis and Catalytic Reactions (18 papers). Philippe Compain is often cited by papers focused on Carbohydrate Chemistry and Synthesis (68 papers), Glycosylation and Glycoproteins Research (36 papers) and Synthesis and Catalytic Reactions (18 papers). Philippe Compain collaborates with scholars based in France, Spain and Japan. Philippe Compain's co-authors include Olivier R. Martin, Damien Hazelard, Anne Bodlenner, Camille Decroocq, Naoki Asano, Kyoko Ikeda, Guillaume Godin, Carmen Ortiz Mellet, Teresa Mena Barragán and J. GORÉ and has published in prestigious journals such as Angewandte Chemie International Edition, SHILAP Revista de lepidopterología and Chemical Communications.

In The Last Decade

Philippe Compain

108 papers receiving 3.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Philippe Compain France 32 3.1k 2.0k 493 347 149 111 3.5k
Henrik H. Jensen Denmark 27 2.3k 0.7× 2.1k 1.0× 108 0.2× 292 0.8× 127 0.9× 86 3.2k
Yves Blériot France 27 1.7k 0.6× 1.3k 0.6× 159 0.3× 165 0.5× 96 0.6× 96 2.0k
Tom D. Heightman United Kingdom 30 1.7k 0.5× 3.0k 1.5× 129 0.3× 441 1.3× 101 0.7× 54 4.0k
M. Isabel García‐Moreno Spain 30 1.5k 0.5× 1.2k 0.6× 559 1.1× 243 0.7× 38 0.3× 61 1.8k
Bala Krishnan United States 24 2.3k 0.7× 1.2k 0.6× 169 0.3× 178 0.5× 462 3.1× 39 3.4k
Kwan Soo Kim South Korea 27 1.6k 0.5× 1.4k 0.7× 98 0.2× 118 0.3× 116 0.8× 106 2.4k
Mark C. Bagley United Kingdom 33 2.8k 0.9× 1.3k 0.6× 101 0.2× 104 0.3× 509 3.4× 113 3.6k
Christopher W. am Ende United States 27 1.7k 0.6× 1.3k 0.6× 177 0.4× 33 0.1× 172 1.2× 52 2.7k
Jetze J. Tepe United States 30 1.6k 0.5× 1.1k 0.5× 64 0.1× 113 0.3× 129 0.9× 94 2.5k
Inmaculada Robina Spain 25 1.7k 0.5× 1.1k 0.5× 139 0.3× 179 0.5× 53 0.4× 117 1.9k

Countries citing papers authored by Philippe Compain

Since Specialization
Citations

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

Fields of papers citing papers by Philippe Compain

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Philippe Compain

This figure shows the co-authorship network connecting the top 25 collaborators of Philippe Compain. A scholar is included among the top collaborators of Philippe Compain 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 Philippe Compain. Philippe Compain 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.
Schettini, Rosaria, Nicolas Kern, Irene Izzo, et al.. (2024). Deconstructing Best‐in‐Class Neoglycoclusters as a Tool for Dissecting Key Multivalent Processes in Glycosidase Inhibition. Chemistry - A European Journal. 30(19). e202304126–e202304126. 3 indexed citations
2.
Yang, Zhongzhen, Damien Hazelard, Adrian C. Whitwood, et al.. (2024). Expanding the scope of the successive ring expansion strategy for macrocycle and medium-sized ring synthesis: unreactive and reactive lactams. Organic & Biomolecular Chemistry. 22(15). 2985–2991. 2 indexed citations
3.
Compain, Philippe, et al.. (2024). Diastereoselective access to C,C-glycosyl amino acids via iron-catalyzed, auxiliary-enabled MHAT coupling. Chemical Communications. 60(23). 3154–3157. 3 indexed citations
4.
Narobe, Rok, et al.. (2023). Towards a General Access to 1‐Azaspirocyclic Systems via Photoinduced, Reductive Decarboxylative Radical Cyclizations. Chemistry - A European Journal. 30(13). e202303841–e202303841. 1 indexed citations
5.
Bodlenner, Anne, Marco Marradi, María de los Ángeles Ramírez, et al.. (2021). Hybrid Multivalent Jack Bean α-Mannosidase Inhibitors: The First Example of Gold Nanoparticles Decorated with Deoxynojirimycin Inhitopes. Molecules. 26(19). 5864–5864. 9 indexed citations
6.
Sala, Paolo Della, Carmine Gaeta, Carmen Talotta, et al.. (2020). Synthesis and Glycosidase Inhibition Properties of Calix[8]arene-Based Iminosugar Click Clusters. Pharmaceuticals. 13(11). 366–366. 10 indexed citations
7.
Rodriguez, Frédéric, Mathieu L. Lepage, Anne Bodlenner, et al.. (2019). N,O-Dialkyl deoxynojirimycin derivatives as CERT START domain ligands. Bioorganic & Medicinal Chemistry Letters. 30(2). 126796–126796. 7 indexed citations
8.
Hazelard, Damien, Josefina Casas, Helen Michelakakis, et al.. (2016). Investigation of original multivalent iminosugars as pharmacological chaperones for the treatment of Gaucher disease. Carbohydrate Research. 429. 98–104. 22 indexed citations
9.
Lepage, Mathieu L., Antoine Mirloup, Manon Ripoll, et al.. (2015). Design, synthesis and photochemical properties of the first examples of iminosugar clusters based on fluorescent cores. Beilstein Journal of Organic Chemistry. 11. 659–667. 23 indexed citations
10.
Lepage, Mathieu L., Alessandra Meli, Anne Bodlenner, et al.. (2014). Synthesis of the first examples of iminosugar clusters based on cyclopeptoid cores. Beilstein Journal of Organic Chemistry. 10. 1406–1412. 37 indexed citations
11.
Compain, Philippe, Camille Decroocq, Antoine Joosten, et al.. (2013). Rescue of Functional CFTR Channels in Cystic Fibrosis: A Dramatic Multivalent Effect Using Iminosugar Cluster‐Based Correctors. ChemBioChem. 14(15). 2050–2058. 41 indexed citations
12.
Decroocq, Camille, et al.. (2011). The Multivalent Effect in Glycosidase Inhibition: Probing the Influence of Architectural Parameters with Cyclodextrin‐based Iminosugar Click Clusters. Chemistry - A European Journal. 17(49). 13825–13831. 90 indexed citations
13.
Compain, Philippe, Camille Decroocq, Julien Iehl, et al.. (2010). Glycosidase Inhibition with Fullerene Iminosugar Balls: A Dramatic Multivalent Effect. Angewandte Chemie International Edition. 49(33). 5753–5756. 168 indexed citations
14.
Gallienne, Estelle, et al.. (2010). Synthesis of new β-1-C-alkylated imino-l-iditols: A comparative study of their activity as β-glucocerebrosidase inhibitors. Bioorganic & Medicinal Chemistry. 18(7). 2645–2650. 29 indexed citations
15.
16.
Yu, Liang, Kyoko Ikeda, Atsushi Kato, et al.. (2006). α-1-C-Octyl-1-deoxynojirimycin as a pharmacological chaperone for Gaucher disease. Bioorganic & Medicinal Chemistry. 14(23). 7736–7744. 87 indexed citations
17.
Godin, Guillaume, Philippe Compain, Olivier R. Martin, et al.. (2004). α-1-C-Alkyl-1-deoxynojirimycin derivatives as potent and selective inhibitors of intestinal isomaltase: remarkable effect of the alkyl chain length on glycosidase inhibitory profile. Bioorganic & Medicinal Chemistry Letters. 14(24). 5991–5995. 44 indexed citations
18.
Compain, Philippe & Olivier R. Martin. (2003). Design, Synthesis and Biological Evaluation of Iminosugar-Based Glycosyltransferase Inhibitors. Current Topics in Medicinal Chemistry. 3(5). 541–560. 176 indexed citations
19.
Craig, A. Grey, et al.. (2001). Enzymatic glycosylation of contulakin-G, a glycopeptide isolated from Conus venom, with a mammalian ppGalNAc-transferase. Toxicon. 39(6). 809–815. 17 indexed citations
20.
Martin, Olivier R., Philippe Compain, Haruhisa Kizu, & Naoki Asano. (1999). Revised structure of a homonojirimycin isomer from Aglaonema treubii: First example of a naturally occurring α-homoallonojirimycin. Bioorganic & Medicinal Chemistry Letters. 9(21). 3171–3174. 13 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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