Alexis Archambeau

691 total citations
18 papers, 587 citations indexed

About

Alexis Archambeau is a scholar working on Organic Chemistry, Pharmaceutical Science and Inorganic Chemistry. According to data from OpenAlex, Alexis Archambeau has authored 18 papers receiving a total of 587 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Organic Chemistry, 4 papers in Pharmaceutical Science and 2 papers in Inorganic Chemistry. Recurrent topics in Alexis Archambeau's work include Cyclopropane Reaction Mechanisms (12 papers), Catalytic C–H Functionalization Methods (9 papers) and Catalytic Alkyne Reactions (7 papers). Alexis Archambeau is often cited by papers focused on Cyclopropane Reaction Mechanisms (12 papers), Catalytic C–H Functionalization Methods (9 papers) and Catalytic Alkyne Reactions (7 papers). Alexis Archambeau collaborates with scholars based in France and United States. Alexis Archambeau's co-authors include Janine Cossy, Christophe Meyer, Frédéric Miege, Tomislav Rovis, Marie Cordier≈, Nicolas Casaretto, Jean‐Louis Brayer, Jean‐Pierre Demoute, Benoı̂t Folléas and Antoine Roblin and has published in prestigious journals such as Angewandte Chemie International Edition, Accounts of Chemical Research and The Journal of Organic Chemistry.

In The Last Decade

Alexis Archambeau

18 papers receiving 579 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alexis Archambeau France 13 574 64 48 32 13 18 587
Chuan‐Hua Qu China 13 525 0.9× 71 1.1× 115 2.4× 21 0.7× 22 1.7× 24 558
Simon M. Nicolle United Kingdom 10 450 0.8× 46 0.7× 42 0.9× 23 0.7× 26 2.0× 11 474
Satish Ghorpade Taiwan 9 670 1.2× 64 1.0× 21 0.4× 17 0.5× 8 0.6× 9 677
Chloe E. Pitsch United States 6 274 0.5× 53 0.8× 45 0.9× 22 0.7× 7 0.5× 6 294
Amanda M. Spiewak United States 3 406 0.7× 57 0.9× 40 0.8× 31 1.0× 8 0.6× 3 424
Niannian Yi China 11 387 0.7× 90 1.4× 52 1.1× 25 0.8× 14 1.1× 22 416
Michael J. Ardolino United States 7 334 0.6× 67 1.0× 30 0.6× 26 0.8× 12 0.9× 12 354
Di‐Han Zhang China 12 770 1.3× 77 1.2× 21 0.4× 24 0.8× 12 0.9× 17 778
Mateus L. Stivanin Brazil 7 560 1.0× 25 0.4× 70 1.5× 27 0.8× 7 0.5× 8 577
Bhuwan Chhetri United States 3 359 0.6× 31 0.5× 55 1.1× 33 1.0× 8 0.6× 3 374

Countries citing papers authored by Alexis Archambeau

Since Specialization
Citations

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

Fields of papers citing papers by Alexis Archambeau

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alexis Archambeau

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

All Works

18 of 18 papers shown
1.
Roblin, Antoine, et al.. (2024). Cycloadditions of 5-Vinyloxazolidine-2,4-diones: A Straightforward Access to the (Thio)hydantoin Scaffold. The Journal of Organic Chemistry. 89(17). 12370–12377. 3 indexed citations
2.
Roblin, Antoine, Nicolas Casaretto, & Alexis Archambeau. (2023). Diastereo- and Enantioselective Palladium-Catalyzed Cycloadditions of 5-Vinyloxazolidine-2,4-diones with Electrophilic Imines. Organic Letters. 25(35). 6453–6458. 12 indexed citations
3.
Casaretto, Nicolas, et al.. (2023). Diastereo- and Enantioselective (3 + 2) Cycloaddition of a New Aza-π-Allylpalladium Zwitterionic Intermediate. The Journal of Organic Chemistry. 88(14). 9941–9945. 13 indexed citations
4.
Casaretto, Nicolas, et al.. (2021). Vinylcyclopropanes as All-Carbon 1,5-Dipoles: A Reactivity Switch for Palladium-Catalyzed (5 + 4) Cycloadditions. Organic Letters. 23(6). 2332–2336. 30 indexed citations
5.
Garrec, Julian, et al.. (2021). A Palladium-Catalyzed Oxa-(4+4)-Cycloaddition Strategy Towards Oxazocine Scaffolds. Synlett. 32(10). 981–986. 11 indexed citations
6.
Archambeau, Alexis, et al.. (2020). Asymmetric Transfer Hydrogenation of gem‐Difluorocyclopropenyl Esters: Access to Enantioenriched gem‐Difluorocyclopropanes. Angewandte Chemie International Edition. 59(42). 18505–18509. 43 indexed citations
7.
Archambeau, Alexis, et al.. (2020). Asymmetric Transfer Hydrogenation of gem‐Difluorocyclopropenyl Esters: Access to Enantioenriched gem‐Difluorocyclopropanes. Angewandte Chemie. 132(42). 18663–18667. 8 indexed citations
8.
Cordier≈, Marie & Alexis Archambeau. (2018). (3 + 3) Cycloaddition of Oxyallyl Cations with Nitrones: Diastereoselective Access to 1,2-Oxazinanes. Organic Letters. 20(8). 2265–2268. 29 indexed citations
9.
Archambeau, Alexis, et al.. (2016). Rhodium(II)‐Catalyzed Isomerization of Cyclopropenylmethyl Esters into (Acyloxymethylene)cyclopropanes. Chemistry - A European Journal. 22(17). 6100–6110. 8 indexed citations
10.
Archambeau, Alexis, et al.. (2016). Gold-Catalyzed Rearrangement of (Silylcyclopropenyl)methyl Ethers into (Silylmethylene)cyclopropanes. Synthesis. 48(19). 3165–3174. 4 indexed citations
11.
Archambeau, Alexis & Tomislav Rovis. (2015). Rhodium(III)‐Catalyzed Allylic C(sp3)–H Activation of Alkenyl Sulfonamides: Unexpected Formation of Azabicycles. Angewandte Chemie International Edition. 54(45). 13337–13340. 76 indexed citations
12.
Archambeau, Alexis, Frédéric Miege, Christophe Meyer, & Janine Cossy. (2015). Intramolecular Cyclopropanation and C–H Insertion Reactions with Metal Carbenoids Generated from Cyclopropenes. Accounts of Chemical Research. 48(4). 1021–1031. 168 indexed citations
13.
Archambeau, Alexis & Tomislav Rovis. (2015). Rhodium(III)‐Catalyzed Allylic C(sp3)–H Activation of Alkenyl Sulfonamides: Unexpected Formation of Azabicycles. Angewandte Chemie. 127(45). 13535–13538. 31 indexed citations
14.
Arseniyadis, Stellios, Janine Cossy, J. Fournier, et al.. (2013). Palladium-Catalyzed Allylic Alkylation of Allyl Dienol Carbonates: Reactivity, Regioselectivity, Enantioselectivity, and Synthetic Applications. Synlett. 24(18). 2350–2364. 35 indexed citations
15.
Archambeau, Alexis, Christophe Meyer, Janine Cossy, et al.. (2012). Efficient Synthesis of Substituted 3‐Azabicyclo[3.1.0]hexan‐2‐ones from 2‐Iodocyclopropanecarboxamides Using a Copper‐Free Sonogashira Coupling. Chemistry - A European Journal. 18(52). 16716–16727. 17 indexed citations
16.
Archambeau, Alexis, Frédéric Miege, Christophe Meyer, & Janine Cossy. (2012). Highly Efficient Stereoselective Catalytic C(sp3)H Insertions with Donor Rhodium Carbenoids Generated from Cyclopropenes. Angewandte Chemie International Edition. 51(46). 11540–11544. 47 indexed citations
17.
Archambeau, Alexis, Frédéric Miege, Christophe Meyer, & Janine Cossy. (2012). Highly Efficient Stereoselective Catalytic C(sp3)H Insertions with Donor Rhodium Carbenoids Generated from Cyclopropenes. Angewandte Chemie. 124(46). 11708–11712. 20 indexed citations
18.
Archambeau, Alexis, Christophe Meyer, Janine Cossy, et al.. (2011). Copper-Free Sonogashira Coupling of Cyclopropyl Iodides with Terminal Alkynes. Organic Letters. 13(5). 956–959. 32 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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