Benoit Cardinal‐David

1.2k total citations
16 papers, 1.0k citations indexed

About

Benoit Cardinal‐David is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, Benoit Cardinal‐David has authored 16 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Organic Chemistry, 7 papers in Molecular Biology and 4 papers in Inorganic Chemistry. Recurrent topics in Benoit Cardinal‐David's work include Synthetic Organic Chemistry Methods (7 papers), Chemical Synthesis and Analysis (5 papers) and Asymmetric Synthesis and Catalysis (5 papers). Benoit Cardinal‐David is often cited by papers focused on Synthetic Organic Chemistry Methods (7 papers), Chemical Synthesis and Analysis (5 papers) and Asymmetric Synthesis and Catalysis (5 papers). Benoit Cardinal‐David collaborates with scholars based in United States and Canada. Benoit Cardinal‐David's co-authors include Karl A. Scheidt, Dane Holte, Daniel Cohen, Yvan Guindon, Amy A. Sarjeant, John M. Roberts, Brigitte Guérin, Michel Prévost, Benoit Daoust and Serge Landry and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Nature Chemistry.

In The Last Decade

Benoit Cardinal‐David

16 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Benoit Cardinal‐David United States 11 996 184 87 34 31 16 1.0k
Alexis Coste France 11 1.6k 1.6× 105 0.6× 158 1.8× 20 0.6× 62 2.0× 15 1.7k
Jongrock Kong United States 12 705 0.7× 242 1.3× 179 2.1× 12 0.4× 34 1.1× 16 777
Leticia Pérez‐Serrano Spain 8 622 0.6× 93 0.5× 90 1.0× 15 0.4× 16 0.5× 11 652
Shigemitsu Okada Japan 10 555 0.6× 205 1.1× 134 1.5× 11 0.3× 25 0.8× 16 621
Michael T. Corbett United States 11 465 0.5× 224 1.2× 96 1.1× 18 0.5× 40 1.3× 16 550
S. Jaya Prakash India 12 569 0.6× 81 0.4× 103 1.2× 19 0.6× 14 0.5× 18 599
Tomofumi Kinoshita Japan 6 440 0.4× 192 1.0× 93 1.1× 10 0.3× 22 0.7× 6 475
Anne‐Marie Dechert‐Schmitt United States 10 537 0.5× 128 0.7× 86 1.0× 12 0.4× 42 1.4× 13 584
Qianjia Yuan China 16 597 0.6× 375 2.0× 94 1.1× 29 0.9× 65 2.1× 38 724

Countries citing papers authored by Benoit Cardinal‐David

Since Specialization
Citations

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

Fields of papers citing papers by Benoit Cardinal‐David

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Benoit Cardinal‐David. 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 Benoit Cardinal‐David. The network helps show where Benoit Cardinal‐David may publish in the future.

Co-authorship network of co-authors of Benoit Cardinal‐David

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

All Works

16 of 16 papers shown
1.
Moschetta, Eric G., Benoit Cardinal‐David, Travis B. Dunn, & Moiz Diwan. (2024). Scalable Protocol for Removing Triphenylphosphine Oxide from Reactions Using MgCl2 and Wet Milling. Organic Process Research & Development. 28(7). 2677–2682. 2 indexed citations
2.
Cardinal‐David, Benoit, et al.. (2021). Continuous Multiphase Flow Nitration and Cryogenic Flow Formylation: Enabling Process Development and Manufacturing of Pharmaceutical Intermediates. Organic Process Research & Development. 25(11). 2473–2481. 7 indexed citations
3.
Huters, Alexander D., James P. Stambuli, Russell C. Klix, et al.. (2021). Scalable Asymmetric Syntheses of Foslevodopa and Foscarbidopa Drug Substances for the Treatment of Parkinson’s Disease. The Journal of Organic Chemistry. 87(4). 1986–1995. 9 indexed citations
4.
Cardinal‐David, Benoit, et al.. (2020). Diastereoselective and regioselective synthesis of adenosine thionucleoside analogues using an acyclic approach. Canadian Journal of Chemistry. 98(9). 466–470. 4 indexed citations
5.
Cohen, Daniel, Benoit Cardinal‐David, & Karl A. Scheidt. (2011). Lewis Acid Activated Synthesis of Highly Substituted Cyclopentanes by the N‐Heterocyclic Carbene Catalyzed Addition of Homoenolate Equivalents to Unsaturated Ketoesters. Angewandte Chemie International Edition. 50(7). 1678–1682. 146 indexed citations
6.
Cohen, Daniel, Benoit Cardinal‐David, & Karl A. Scheidt. (2011). Lewis Acid Activated Synthesis of Highly Substituted Cyclopentanes by the N‐Heterocyclic Carbene Catalyzed Addition of Homoenolate Equivalents to Unsaturated Ketoesters. Angewandte Chemie. 123(7). 1716–1720. 58 indexed citations
7.
Cohen, Daniel, Benoit Cardinal‐David, John M. Roberts, Amy A. Sarjeant, & Karl A. Scheidt. (2011). NHC-Catalyzed/Titanium(IV)−Mediated Highly Diastereo- and Enantioselective Dimerization of Enals. Organic Letters. 13(5). 1068–1071. 72 indexed citations
8.
Cardinal‐David, Benoit, et al.. (2010). Cooperative catalysis by carbenes and Lewis acids in a highly stereoselective route to γ-lactams. Nature Chemistry. 2(9). 766–771. 353 indexed citations
9.
Cardinal‐David, Benoit, et al.. (2010). Cooperative N-Heterocyclic Carbene/Lewis Acid Catalysis for Highly Stereoselective Annulation Reactions with Homoenolates. Journal of the American Chemical Society. 132(15). 5345–5347. 282 indexed citations
10.
Duplessis, Martin, et al.. (2009). Stereoselective Quaternary Center Construction via Atom-Transfer Radical Cyclization Using Silicon Tethers on Acyclic Precursors. Organic Letters. 11(14). 3148–3151. 10 indexed citations
11.
Cardinal‐David, Benoit, et al.. (2009). A Stereoselective Approach to Nucleosides and 4′-Thioanalogues from Acyclic Precursors. Journal of the American Chemical Society. 131(47). 17242–17245. 18 indexed citations
12.
Cardinal‐David, Benoit, et al.. (2006). Phenylselenoethers as Precursors of Acyclic Free Radicals. Creating Tertiary and Quaternary Centers Using Free Radical-Based Intermediates. Current Organic Chemistry. 10(15). 1939–1961. 10 indexed citations
13.
Cardinal‐David, Benoit, Brigitte Guérin, & Yvan Guindon. (2004). Synthesis of Tertiary and Quaternary Stereogenic Centers:  A Diastereoselective Tandem Reaction Sequence Combining Mukaiyama and Free Radical-Based Allylation. The Journal of Organic Chemistry. 70(3). 776–784. 17 indexed citations
14.
Guindon, Yvan, Michel Prévost, Benoit Cardinal‐David, et al.. (2002). Synthesis of Propionate Motifs:  Diastereoselective Tandem Reactions Involving Anionic and Free Radical Based Processes  [J. Am. Chem. Soc. 2001, 123 (35), 8496−8501].. Journal of the American Chemical Society. 124(1). 168–168. 8 indexed citations
15.
Cardinal‐David, Benoit, et al.. (2002). Synthesis of polypropionate motifs containing the anti–anti unit. Tetrahedron Letters. 43(39). 7067–7071. 12 indexed citations
16.
Guindon, Yvan, Michel Prévost, Benoit Cardinal‐David, et al.. (2001). Synthesis of Propionate Motifs:  Diastereoselective Tandem Reactions Involving Anionic and Free Radical Based Processes. Journal of the American Chemical Society. 123(35). 8496–8501. 33 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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