Louis Barriault

3.7k total citations
78 papers, 3.1k citations indexed

About

Louis Barriault is a scholar working on Organic Chemistry, Biotechnology and Pharmacology. According to data from OpenAlex, Louis Barriault has authored 78 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 76 papers in Organic Chemistry, 14 papers in Biotechnology and 9 papers in Pharmacology. Recurrent topics in Louis Barriault's work include Synthetic Organic Chemistry Methods (32 papers), Catalytic C–H Functionalization Methods (22 papers) and Radical Photochemical Reactions (20 papers). Louis Barriault is often cited by papers focused on Synthetic Organic Chemistry Methods (32 papers), Catalytic C–H Functionalization Methods (22 papers) and Radical Photochemical Reactions (20 papers). Louis Barriault collaborates with scholars based in Canada, United States and Russia. Louis Barriault's co-authors include Terry McCallum, Irina Denissova, Gabriel Bellavance, Mathieu Morin, Samantha Rohe, Francis Barabé, Steve Arns, Louis Morency, Effiette L. O. Sauer and Leo A. Paquette and has published in prestigious journals such as Journal of the American Chemical Society, Chemical Society Reviews and Angewandte Chemie International Edition.

In The Last Decade

Louis Barriault

76 papers receiving 3.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Louis Barriault Canada 31 2.9k 397 305 230 175 78 3.1k
Bor‐Cherng Hong Taiwan 34 2.7k 0.9× 324 0.8× 478 1.6× 149 0.6× 76 0.4× 113 3.1k
Yong Qiang Tu China 26 2.4k 0.8× 617 1.6× 506 1.7× 193 0.8× 113 0.6× 66 2.9k
Corinna S. Schindler United States 32 2.7k 0.9× 456 1.1× 633 2.1× 187 0.8× 133 0.8× 84 3.0k
Dipakranjan Mal India 23 1.9k 0.7× 160 0.4× 320 1.0× 259 1.1× 85 0.5× 105 2.2k
Ernesto Suárez Spain 29 2.9k 1.0× 252 0.6× 872 2.9× 186 0.8× 236 1.3× 151 3.3k
Jean‐Luc Parrain France 24 1.9k 0.7× 230 0.6× 383 1.3× 126 0.5× 144 0.8× 153 2.2k
Jun‐ichi Matsuo Japan 27 2.1k 0.7× 344 0.9× 348 1.1× 101 0.4× 100 0.6× 112 2.3k
Tetsuhiro Nemoto Japan 35 3.4k 1.2× 925 2.3× 471 1.5× 139 0.6× 105 0.6× 146 3.7k
Kou Hiroya Japan 32 3.5k 1.2× 495 1.2× 508 1.7× 154 0.7× 197 1.1× 90 3.9k
Chun‐An Fan China 37 4.4k 1.5× 739 1.9× 564 1.8× 254 1.1× 195 1.1× 104 4.7k

Countries citing papers authored by Louis Barriault

Since Specialization
Citations

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

Fields of papers citing papers by Louis Barriault

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Louis Barriault

This figure shows the co-authorship network connecting the top 25 collaborators of Louis Barriault. A scholar is included among the top collaborators of Louis Barriault 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 Louis Barriault. Louis Barriault 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.
Barriault, Louis, et al.. (2024). Redox‐Neutral Multicatalytic Cerium Photoredox‐Enabled Cleavage of O−H Bearing Substrates. Chemistry - A European Journal. 30(26). e202400642–e202400642. 3 indexed citations
2.
Barriault, Louis, et al.. (2024). Photoactivated Formal [3 + 2]/[4+2] Cycloaddition of N‐Aryl Cyclopropyl and Cyclobutylamines. European Journal of Organic Chemistry. 27(44). 1 indexed citations
3.
Rohe, Samantha, et al.. (2020). Single-Electron Transfer from Dimsyl Anion in the Alkylation of Phenols. The Journal of Organic Chemistry. 85(4). 2806–2813. 14 indexed citations
4.
Barabé, Francis, et al.. (2017). A 11‐Steps Total Synthesis of Magellanine through a Gold(I)‐Catalyzed Dehydro Diels–Alder Reaction. Angewandte Chemie. 129(22). 6377–6380. 8 indexed citations
5.
Bellavance, Gabriel, et al.. (2015). Synthesis and Isolation of Organogold Complexes through a Controlled 1,2‐Silyl Migration. Chemistry - A European Journal. 21(27). 9662–9665. 18 indexed citations
6.
Kaldas, Sherif J., et al.. (2015). Indole Functionalization via Photoredox Gold Catalysis. Organic Letters. 17(11). 2864–2866. 103 indexed citations
7.
McCallum, Terry, et al.. (2013). Photoredox Transformations with Dimeric Gold Complexes. Angewandte Chemie. 125(50). 13584–13587. 52 indexed citations
8.
Morin, Mathieu, et al.. (2013). Gold(I)-catalyzed domino cyclization for the synthesis of polyaromatic heterocycles. Beilstein Journal of Organic Chemistry. 9. 2625–2628. 7 indexed citations
9.
McCallum, Terry, et al.. (2013). Photoredox Transformations with Dimeric Gold Complexes. Angewandte Chemie International Edition. 52(50). 13342–13345. 172 indexed citations
10.
Barriault, Louis, et al.. (2012). A Formal Synthesis of Vinigrol. Angewandte Chemie International Edition. 51(9). 2111–2114. 31 indexed citations
11.
Hooper, James, Effiette L. O. Sauer, Steve Arns, Tom K. Woo, & Louis Barriault. (2010). On the Origin of Altered Diastereomeric Ratios for Anionic versus Neutral Reaction Conditions in the Oxy‐Cope/Ene Reaction: An Interplay of Experiment and Computational Modeling. Chemistry - A European Journal. 16(47). 14124–14130. 9 indexed citations
12.
Beingessner, Rachel L., et al.. (2010). Progress toward the Total Synthesis of (±)-Havellockate. The Journal of Organic Chemistry. 75(19). 6337–6346. 19 indexed citations
13.
Barriault, Louis, et al.. (2009). Pericyclic domino reactions: concise approaches to natural carbocyclic frameworks. Chemical Society Reviews. 38(11). 3092–3092. 108 indexed citations
14.
Barriault, Louis, et al.. (2008). Stereocontrolled synthesis of carbocycles via four successive pericyclic reactions. Chemical Communications. 3004–3004. 6 indexed citations
15.
Barriault, Louis, et al.. (2007). THE CONQUEST OF VINIGROL. CREATIVITY, FRUSTRATIONS, AND HOPE. Organic Preparations and Procedures International. 39(4). 311–353. 26 indexed citations
16.
Arns, Steve & Louis Barriault. (2006). Concise Synthesis of the neo-Clerodane Skeleton of Teucrolivin A Using a Pericyclic Reaction Cascade. The Journal of Organic Chemistry. 71(5). 1809–1816. 15 indexed citations
17.
Denissova, Irina & Louis Barriault. (2003). Stereoselective formation of quaternary carbon centers and related functions. Tetrahedron. 59(51). 10105–10146. 452 indexed citations
18.
Paquette, Leo A., Louis Barriault, Dmitri Pissarnitski, & Jeffrey N. Johnston. (2000). ChemInform Abstract: Stereocontrolled Elaboration of Natural (‐)‐Polycavernoside A, a Powerfully Toxic Metabolite of the Red Alga Polycavernosa tsudai.. ChemInform. 31(19). 2 indexed citations
19.
Paquette, Leo A., Louis Barriault, Dmitri Pissarnitski, & Jeffrey N. Johnston. (1999). Stereocontrolled Elaboration of Natural (−)-Polycavernoside A, a Powerfully Toxic Metabolite of the Red Alga Polycavernosa tsudai. Journal of the American Chemical Society. 122(4). 619–631. 49 indexed citations
20.
Barriault, Louis, et al.. (1999). Synthesis and biological evaluation of analogs of the marine toxin polycavernoside A. Bioorganic & Medicinal Chemistry Letters. 9(14). 2069–2072. 15 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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