Rodolphe Beaud

793 total citations
16 papers, 676 citations indexed

About

Rodolphe Beaud is a scholar working on Organic Chemistry, Spectroscopy and Inorganic Chemistry. According to data from OpenAlex, Rodolphe Beaud has authored 16 papers receiving a total of 676 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Organic Chemistry, 1 paper in Spectroscopy and 1 paper in Inorganic Chemistry. Recurrent topics in Rodolphe Beaud's work include Catalytic C–H Functionalization Methods (9 papers), Asymmetric Synthesis and Catalysis (9 papers) and Catalytic Cross-Coupling Reactions (4 papers). Rodolphe Beaud is often cited by papers focused on Catalytic C–H Functionalization Methods (9 papers), Asymmetric Synthesis and Catalysis (9 papers) and Catalytic Cross-Coupling Reactions (4 papers). Rodolphe Beaud collaborates with scholars based in France, Switzerland and United Kingdom. Rodolphe Beaud's co-authors include Guillaume Vincent, Cyrille Kouklovsky, Régis Guillot, Robert J. Phipps, Matthew J. Gaunt, Vincent Gandon, Annie Pouilhès, Emmanuel Roulland, Raj Kumar Nandi and Xingxing Wu and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Chemical Communications.

In The Last Decade

Rodolphe Beaud

16 papers receiving 667 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Rodolphe Beaud France	11	645	168	64	52	48	16	676
Jun Kikuchi Japan	14	535 0.8×	154 0.9×	45 0.7×	68 1.3×	54 1.1×	41	580
Xi‐Jia Liu China	14	724 1.1×	221 1.3×	46 0.7×	77 1.5×	37 0.8×	19	751
Thomas Buyck Switzerland	8	546 0.8×	108 0.6×	39 0.6×	89 1.7×	24 0.5×	10	594
Huayu Zheng China	10	787 1.2×	96 0.6×	52 0.8×	73 1.4×	26 0.5×	14	861
Santanu Ghosh India	17	789 1.2×	111 0.7×	92 1.4×	58 1.1×	20 0.4×	22	827
Xiao‐Wei Liang China	14	766 1.2×	178 1.1×	69 1.1×	94 1.8×	18 0.4×	19	794
Zhijun Zuo China	20	1.5k 2.3×	179 1.1×	55 0.9×	64 1.2×	46 1.0×	36	1.5k
Ren‐Qi Xu China	16	876 1.4×	131 0.8×	73 1.1×	53 1.0×	28 0.6×	19	901
Sachin Narute Israel	8	650 1.0×	92 0.5×	87 1.4×	57 1.1×	114 2.4×	11	697
Fangxi Xu China	7	567 0.9×	148 0.9×	30 0.5×	143 2.8×	42 0.9×	8	602

Countries citing papers authored by Rodolphe Beaud

Since Specialization

Citations

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

Fields of papers citing papers by Rodolphe Beaud

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rodolphe Beaud

This figure shows the co-authorship network connecting the top 25 collaborators of Rodolphe Beaud. A scholar is included among the top collaborators of Rodolphe Beaud 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 Rodolphe Beaud. Rodolphe Beaud is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

1.

Michelet, Bastien, Rodolphe Beaud, Agnès Martin‐Mingot, et al.. (2022). Hidden Heptacyclic Chiral N‐Acyl Iminium Ions: A New Entry to Enantioenriched Polycyclic Azepanes and Azocanes by Superacid‐Promoted Intramolecular Pictet‐Spengler Reaction. Chemistry - A European Journal. 28(25). e202200432–e202200432. 3 indexed citations

2.

Wu, Xingxing, et al.. (2021). Catalyst control over sixfold stereogenicity. Nature Catalysis. 4(6). 457–462. 49 indexed citations

3.

Beaud, Rodolphe, Bastien Michelet, Agnès Martin‐Mingot, et al.. (2019). Enantioenriched Methylene‐Bridged Benzazocanes Synthesis by Organocatalytic and Superacid Activations. Angewandte Chemie. 132(3). 1295–1301. 7 indexed citations

4.

Beaud, Rodolphe, Bastien Michelet, Agnès Martin‐Mingot, et al.. (2019). Enantioenriched Methylene‐Bridged Benzazocanes Synthesis by Organocatalytic and Superacid Activations. Angewandte Chemie International Edition. 59(3). 1279–1285. 10 indexed citations

5.

Beaud, Rodolphe, Raj Kumar Nandi, Alejandro Pérez‐Luna, et al.. (2017). Revealing the electrophilicity of N-Ac indoles with FeCl₃: a mechanistic study. Chemical Communications. 53(43). 5834–5837. 13 indexed citations

6.

Nandi, Raj Kumar, Alejandro Pérez‐Luna, Davide Gori, et al.. (2017). Triflic Acid as an Efficient Brønsted Acid Promoter for the Umpolung of N‐Ac Indoles in Hydroarylation Reactions. Advanced Synthesis & Catalysis. 360(1). 161–172. 14 indexed citations

7.

Beaud, Rodolphe, Robert J. Phipps, & Matthew J. Gaunt. (2016). Enantioselective Cu-Catalyzed Arylation of Secondary Phosphine Oxides with Diaryliodonium Salts toward the Synthesis of P-Chiral Phosphines. Journal of the American Chemical Society. 138(40). 13183–13186. 184 indexed citations

8.

Nandi, Raj Kumar, et al.. (2016). Intermolecular dearomative C2-arylation of N-Ac indoles activated by FeCl₃. Chemical Communications. 52(30). 5328–5331. 31 indexed citations

9.

Beaud, Rodolphe, et al.. (2015). Synthesis of 3-arylated indolines from dearomatization of indoles. Tetrahedron Letters. 56(30). 4413–4429. 76 indexed citations

10.

Beaud, Rodolphe, Régis Guillot, Cyrille Kouklovsky, & Guillaume Vincent. (2014). Regioselective Hydroarylation Reactions of C3 Electrophilic N‐Acetylindoles Activated by FeCl₃: An Entry to 3‐(Hetero)arylindolines. Chemistry - A European Journal. 20(24). 7492–7500. 39 indexed citations

11.

Vincent, Guillaume, et al.. (2014). The Quest for an Oxidative Coupling of Phenols and Indoles towards Benzofuroindolines: A Two-Stage Approach. Synlett. 26(4). 432–440. 10 indexed citations

12.

Pouilhès, Annie, et al.. (2014). Bioinspired Direct Access to Benzofuroindolines by Oxidative [3 + 2] Annulation of Phenols and Indoles. Organic Letters. 16(21). 5752–5755. 72 indexed citations

13.

Beaud, Rodolphe, et al.. (2012). Counteranion‐Directed Catalysis in the Tsuji–Trost Reaction: Stereocontrolled Access to 2,5‐Disubstituted 3‐Hydroxy‐Tetrahydrofurans. Angewandte Chemie International Edition. 51(42). 10510–10514. 32 indexed citations

14.

Beaud, Rodolphe, et al.. (2012). Counteranion‐Directed Catalysis in the Tsuji–Trost Reaction: Stereocontrolled Access to 2,5‐Disubstituted 3‐Hydroxy‐Tetrahydrofurans. Angewandte Chemie. 124(42). 10662–10666. 3 indexed citations

15.

Beaud, Rodolphe, et al.. (2012). FeCl₃‐Mediated Friedel–Crafts Hydroarylation with Electrophilic N‐Acetyl Indoles for the Synthesis of Benzofuroindolines. Angewandte Chemie. 124(50). 12714–12718. 39 indexed citations

16.

Beaud, Rodolphe, Régis Guillot, Cyrille Kouklovsky, & Guillaume Vincent. (2012). FeCl₃‐Mediated Friedel–Crafts Hydroarylation with Electrophilic N‐Acetyl Indoles for the Synthesis of Benzofuroindolines. Angewandte Chemie International Edition. 51(50). 12546–12550. 94 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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