David C. Leitch

3.6k total citations · 1 hit paper
70 papers, 2.4k citations indexed

About

David C. Leitch is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, David C. Leitch has authored 70 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 56 papers in Organic Chemistry, 28 papers in Inorganic Chemistry and 11 papers in Molecular Biology. Recurrent topics in David C. Leitch's work include Asymmetric Hydrogenation and Catalysis (28 papers), Catalytic C–H Functionalization Methods (25 papers) and Catalytic Cross-Coupling Reactions (20 papers). David C. Leitch is often cited by papers focused on Asymmetric Hydrogenation and Catalysis (28 papers), Catalytic C–H Functionalization Methods (25 papers) and Catalytic Cross-Coupling Reactions (20 papers). David C. Leitch collaborates with scholars based in Canada, United States and United Kingdom. David C. Leitch's co-authors include Laurel L. Schafer, Charles S. Yeung, Jennifer A. Kozak, Jason A. Bexrud, Philippa R. Payne, Joseph Becica, M. C. Wood, James D. Beard, Mary A. Wood and Christine R. Dunbar and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Nature Communications.

In The Last Decade

David C. Leitch

67 papers receiving 2.4k citations

Hit Papers

Beyond Bioisosteres: Divergent Synthesis of Azabicyclohex... 2022 2026 2023 2024 2022 50 100 150

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David C. Leitch Canada 25 2.1k 1.1k 282 217 178 70 2.4k
Chae S. Yi United States 34 2.8k 1.3× 1.3k 1.2× 250 0.9× 258 1.2× 132 0.7× 73 3.0k
Luis C. Misal Castro France 20 2.4k 1.2× 916 0.9× 411 1.5× 146 0.7× 125 0.7× 24 2.8k
Denis Chusov Russia 24 1.8k 0.8× 1.3k 1.2× 469 1.7× 276 1.3× 160 0.9× 92 2.2k
Fady Nahra Belgium 31 2.3k 1.1× 713 0.7× 197 0.7× 206 0.9× 192 1.1× 84 2.6k
Dmitry L. Usanov Russia 19 1.5k 0.7× 801 0.7× 572 2.0× 167 0.8× 142 0.8× 30 1.9k
Tuan Thanh Dang Germany 26 2.2k 1.0× 1.0k 1.0× 696 2.5× 347 1.6× 261 1.5× 82 2.6k
Benudhar Punji India 28 2.3k 1.1× 1.1k 1.0× 105 0.4× 244 1.1× 118 0.7× 77 2.5k
Renhua Qiu China 31 2.4k 1.2× 652 0.6× 284 1.0× 206 0.9× 201 1.1× 132 2.9k
Christophe Crévisy France 27 1.8k 0.9× 818 0.8× 331 1.2× 98 0.5× 78 0.4× 72 1.9k
Jérôme Hannedouche France 25 2.4k 1.1× 1.6k 1.5× 371 1.3× 266 1.2× 83 0.5× 50 2.7k

Countries citing papers authored by David C. Leitch

Since Specialization
Citations

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

Fields of papers citing papers by David C. Leitch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David C. Leitch. 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 David C. Leitch. The network helps show where David C. Leitch may publish in the future.

Co-authorship network of co-authors of David C. Leitch

This figure shows the co-authorship network connecting the top 25 collaborators of David C. Leitch. A scholar is included among the top collaborators of David C. Leitch 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 David C. Leitch. David C. Leitch 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.
Leitch, David C., et al.. (2025). Easily Accessible and Solution‐Stable Ni(0) Precatalysts for High‐Throughput Experimentation. Chemistry - A European Journal. 31(12). e202403960–e202403960.
2.
Miller, Douglas L., et al.. (2025). Base-free palladium-catalyzed borylation of enol carboxylates and further reactivity toward deboronation and cross-coupling. Tetrahedron. 182. 134682–134682. 1 indexed citations
3.
Paci, Irina, et al.. (2024). Interrogating Explicit Solvent Effects on the Mechanism and Site‐Selectivity of Aryl Halide Oxidative Addition to L 2 Pd(0). Chemistry - A European Journal. 30(62). e202402283–e202402283. 1 indexed citations
4.
Paci, Irina, et al.. (2024). Quantitative Reactivity Models for Oxidative Addition to L 2 Pd(0): Additional Substrate Classes, Solvents, and Mechanistic Insights. Chemistry - A European Journal. 30(62). e202402282–e202402282. 5 indexed citations
5.
Schley, Nathan D., et al.. (2024). Mechanisms and Site Selectivity of (Het)Ar–X Oxidative Addition to Pd(0) Are Controlled by Frontier Molecular Orbital Symmetry. Organometallics. 43(24). 3192–3203. 7 indexed citations
6.
Leitch, David C., et al.. (2024). A “neat” synthesis of substituted 2-hydroxy-pyrido[1,2-a]pyrimidin-4-ones. Canadian Journal of Chemistry. 102(4). 206–213.
7.
Schley, Nathan D., et al.. (2023). Enolate addition to bicyclobutanes enables expedient access to 2-oxo-bicyclohexane scaffolds. Chemical Communications. 59(93). 13847–13850. 43 indexed citations
8.
Paci, Irina, et al.. (2022). A broadly applicable quantitative relative reactivity model for nucleophilic aromatic substitution (S N Ar) using simple descriptors. Chemical Science. 13(43). 12681–12695. 28 indexed citations
9.
Gangadharan, Deepak Thrithamarassery, Vishal Yeddu, Dongyang Zhang, et al.. (2022). Inhibition of Amine–Water Proton Exchange Stabilizes Perovskite Ink for Scalable Solar Cell Fabrication. Chemistry of Materials. 34(10). 4394–4402. 14 indexed citations
10.
Kundu, Soumya, Deepak Thrithamarassery Gangadharan, V. M. Burlakov, et al.. (2021). High length-to-width aspect ratio lead bromide microwires via perovskite-induced local concentration gradient for X-ray detection. CrystEngComm. 23(11). 2215–2221. 3 indexed citations
11.
Becica, Joseph, et al.. (2021). DMP DAB–Pd–MAH: A Versatile Pd(0) Source for Precatalyst Formation, Reaction Screening, and Preparative-Scale Synthesis. ACS Catalysis. 11(9). 5636–5646. 30 indexed citations
12.
Leitch, David C., et al.. (2020). Playing with Fire? A Safe and Effective Deactivation of Raney Cobalt using Aqueous Sodium Nitrate. Organic Process Research & Development. 24(6). 1180–1184. 2 indexed citations
13.
Becica, Joseph, et al.. (2019). High-Throughput Discovery and Evaluation of a General Catalytic Method for N -Arylation of Weakly Nucleophilic Sulfonamides. Organic Letters. 21(22). 8981–8986. 25 indexed citations
14.
Arrington, Kenneth L., David C. Leitch, I.J. Andrews, et al.. (2019). A Flow Process Built upon a Batch Foundation—Preparation of a Key Amino Alcohol Intermediate via Multistage Continuous Synthesis. Organic Process Research & Development. 24(10). 1927–1937. 6 indexed citations
15.
Egbert, Jonathan D., Edwin C. Thomsen, Douglas M. Mans, et al.. (2019). Development and Scale-up of Continuous Electrocatalytic Hydrogenation of Functionalized Nitro Arenes, Nitriles, and Unsaturated Aldehydes. Organic Process Research & Development. 23(9). 1803–1812. 30 indexed citations
16.
Vantourout, Julien C., Ling Li, Sonia Chabbra, et al.. (2018). Mechanistic Insight Enables Practical, Scalable, Room Temperature Chan–Lam N-Arylation of N-Aryl Sulfonamides. ACS Catalysis. 8(10). 9560–9566. 62 indexed citations
17.
Leitch, David C.. (2011). Group 4 ureate complexes : synthesis, reactivity, and catalytic carbon-element bond formation. Open Collections. 1 indexed citations
18.
Wood, M. C., David C. Leitch, Charles S. Yeung, Jennifer A. Kozak, & Laurel L. Schafer. (2009). Chiral Neutral Zirconium Amidate Complexes for the Asymmetric Hydroamination of Alkenes. Angewandte Chemie International Edition. 48(38). 6937–6937. 7 indexed citations
19.
Wood, Mary A., David C. Leitch, Charles S. Yeung, Jennifer A. Kozak, & Laurel L. Schafer. (2006). Chiral Neutral Zirconium Amidate Complexes for the Asymmetric Hydroamination of Alkenes. Angewandte Chemie International Edition. 46(3). 354–358. 247 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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