Frédéric Liron

953 total citations
21 papers, 783 citations indexed

About

Frédéric Liron is a scholar working on Organic Chemistry, Molecular Biology and Pharmaceutical Science. According to data from OpenAlex, Frédéric Liron has authored 21 papers receiving a total of 783 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Organic Chemistry, 3 papers in Molecular Biology and 2 papers in Pharmaceutical Science. Recurrent topics in Frédéric Liron's work include Catalytic C–H Functionalization Methods (11 papers), Catalytic Cross-Coupling Reactions (7 papers) and Synthetic Organic Chemistry Methods (6 papers). Frédéric Liron is often cited by papers focused on Catalytic C–H Functionalization Methods (11 papers), Catalytic Cross-Coupling Reactions (7 papers) and Synthetic Organic Chemistry Methods (6 papers). Frédéric Liron collaborates with scholars based in France, Italy and Germany. Frédéric Liron's co-authors include Giovanni Poli, Paul Knochel, Mélanie M. Lorion, Julie Oble, Mouâd Alami, Emmanuel Roulland, Guillaume Prestat, Florian F. Kneisel, Helena Leuser and Jean‐Daniel Brion and has published in prestigious journals such as Angewandte Chemie International Edition, Chemical Communications and The Journal of Organic Chemistry.

In The Last Decade

Frédéric Liron

21 papers receiving 774 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Frédéric Liron France 17 739 165 88 66 27 21 783
Kenzo Yahata Japan 15 468 0.6× 93 0.6× 94 1.1× 40 0.6× 27 1.0× 32 512
Barry M. Trost United States 11 751 1.0× 114 0.7× 77 0.9× 41 0.6× 37 1.4× 11 782
Anyu He United States 12 412 0.6× 106 0.6× 84 1.0× 29 0.4× 25 0.9× 17 446
Chong‐Dao Lu China 20 987 1.3× 171 1.0× 126 1.4× 34 0.5× 40 1.5× 72 1.0k
Yaroslav D. Boyko United States 9 330 0.4× 125 0.8× 72 0.8× 41 0.6× 21 0.8× 18 397
Ozora Kubo Japan 15 595 0.8× 83 0.5× 219 2.5× 47 0.7× 37 1.4× 29 641
Ippei Usui Germany 11 456 0.6× 205 1.2× 107 1.2× 28 0.4× 37 1.4× 11 511
Seth Ribe United States 10 446 0.6× 147 0.9× 120 1.4× 23 0.3× 32 1.2× 12 563
Yuriy Slutskyy United States 10 706 1.0× 62 0.4× 59 0.7× 49 0.7× 24 0.9× 12 755
Tapas Das India 15 530 0.7× 62 0.4× 85 1.0× 41 0.6× 41 1.5× 44 587

Countries citing papers authored by Frédéric Liron

Since Specialization
Citations

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

Fields of papers citing papers by Frédéric Liron

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Frédéric Liron

This figure shows the co-authorship network connecting the top 25 collaborators of Frédéric Liron. A scholar is included among the top collaborators of Frédéric Liron 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 Frédéric Liron. Frédéric Liron 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.
Liron, Frédéric, Julie Oble, Mélanie M. Lorion, & Giovanni Poli. (2014). Direct Allylic Functionalization Through Pd‐Catalyzed C–H Activation. European Journal of Organic Chemistry. 2014(27). 5863–5883. 137 indexed citations
2.
Lorion, Mélanie M., et al.. (2014). Dormant versus Evolving Aminopalladated Intermediates: Toward a Unified Mechanistic Scenario in PdII‐Catalyzed Aminations. Chemistry - A European Journal. 20(6). 1539–1546. 28 indexed citations
3.
Liron, Frédéric, Guillaume Prestat, Mathieu Sauthier, et al.. (2012). Pd-catalyzed domino carbonylative–decarboxylative allylation: an easy and selective monoallylation of ketones. Chemical Communications. 48(47). 5889–5889. 19 indexed citations
4.
Mortreux, André, et al.. (2012). Straightforward Synthesis of Allylated Keto Esters: The Palladium‐Catalysed Haloketone Alkoxycarbonylation/ Allylation Domino Reaction. Advanced Synthesis & Catalysis. 354(6). 1077–1083. 20 indexed citations
5.
Bonin, Hélène, et al.. (2012). A General and Efficient Method for the Alkoxycarbonylation of α‐Chloro Ketones. Advanced Synthesis & Catalysis. 354(16). 3105–3114. 16 indexed citations
6.
Broggini, Gianluigi, et al.. (2012). Transition‐Metal‐Catalyzed Hydroamination and Carboamination Reactions of Anthranilic Allenamides as a Route to 2‐Vinyl‐ and 2‐(α‐Styryl)quinazolin‐4‐one Derivatives. European Journal of Organic Chemistry. 2012(19). 3617–3624. 38 indexed citations
7.
Liron, Frédéric, et al.. (2012). Study of the Total Synthesis of (−)-Exiguolide. The Journal of Organic Chemistry. 77(16). 6728–6742. 23 indexed citations
8.
Nahra, Fady, Frédéric Liron, Guillaume Prestat, et al.. (2010). Striking AcOH Acceleration in Direct Intramolecular Allylic Amination Reactions. Chemistry - A European Journal. 16(5). 1414–1414. 2 indexed citations
9.
Guinchard, Xavier, et al.. (2010). Total Synthesis of (−)-Exiguolide. Organic Letters. 12(4). 744–747. 43 indexed citations
10.
Nahra, Fady, Frédéric Liron, Guillaume Prestat, et al.. (2009). Striking AcOH Acceleration in Direct Intramolecular Allylic Amination Reactions. Chemistry - A European Journal. 15(42). 11078–11082. 85 indexed citations
11.
Meyer, Michèle, et al.. (2009). An antiplasmodial new (bis)indole alkaloid from the hard coral Tubastraea sp.. Natural Product Research. 23(2). 178–182. 33 indexed citations
12.
Liron, Frédéric & Paul Knochel. (2007). Reactivity of stable neopentyl-Pd intermediates in the absence of nucleophile. Tetrahedron Letters. 48(28). 4943–4946. 37 indexed citations
13.
Liron, Frédéric, et al.. (2007). Suzuki−Miyaura Cross-Coupling of 1,1-Dichloro-1-alkenes with 9-Alkyl-9-BBN. The Journal of Organic Chemistry. 72(6). 2220–2223. 46 indexed citations
14.
Leuser, Helena, et al.. (2005). Highly Enantioselective Preparation of Tertiary Alcohols and Amines by Copper‐Mediated Diastereoselective Allylic SN2′ Substitutions. Angewandte Chemie International Edition. 44(29). 4627–4631. 68 indexed citations
15.
Leuser, Helena, et al.. (2005). Hoch enantioselektive Synthese von tertiären Alkoholen und Aminen durch kupfervermittelte diastereoselektive allylische SN2′‐Substitutionen. Angewandte Chemie. 117(29). 4703–4707. 32 indexed citations
16.
Liron, Frédéric, et al.. (2003). Palladium‐Catalyzed Stereoselective Synthesis of E‐ and Z‐1,1‐Diaryl or Triarylolefins.. ChemInform. 34(27). 1 indexed citations
17.
Liron, Frédéric, et al.. (2003). Palladium-catalyzed stereoselective synthesis of E- and Z-1,1-diaryl or triarylolefins. Tetrahedron Letters. 44(14). 2789–2794. 32 indexed citations
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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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