Pat Forgione

2.0k total citations
68 papers, 1.6k citations indexed

About

Pat Forgione is a scholar working on Organic Chemistry, Molecular Biology and Biomedical Engineering. According to data from OpenAlex, Pat Forgione has authored 68 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Organic Chemistry, 10 papers in Molecular Biology and 8 papers in Biomedical Engineering. Recurrent topics in Pat Forgione's work include Catalytic C–H Functionalization Methods (21 papers), Sulfur-Based Synthesis Techniques (15 papers) and Catalytic Cross-Coupling Reactions (11 papers). Pat Forgione is often cited by papers focused on Catalytic C–H Functionalization Methods (21 papers), Sulfur-Based Synthesis Techniques (15 papers) and Catalytic Cross-Coupling Reactions (11 papers). Pat Forgione collaborates with scholars based in Canada, United States and Brazil. Pat Forgione's co-authors include Alex G. Fallis, François Bilodeau, Marie‐Christine Brochu, Murray D. Bailey, Miguel St‐Onge, Dirk H. Ortgies, Fei Chen, Nicolas Guimond, Peter D. Wilson and F. Marshall Beringer 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

Pat Forgione

65 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Pat Forgione Canada 20 1.3k 170 146 143 117 68 1.6k
Yoshikazu Kimura Japan 21 849 0.7× 253 1.5× 131 0.9× 76 0.5× 108 0.9× 100 1.2k
David A. Conlon United States 20 807 0.6× 207 1.2× 134 0.9× 160 1.1× 193 1.6× 57 1.3k
Zhuo Wang China 21 789 0.6× 316 1.9× 103 0.7× 69 0.5× 91 0.8× 58 1.2k
Sihui Long China 23 540 0.4× 386 2.3× 164 1.1× 192 1.3× 312 2.7× 93 1.4k
Corinne Wills United Kingdom 20 506 0.4× 99 0.6× 401 2.7× 45 0.3× 282 2.4× 66 1.0k
Belgin Canturk United States 13 986 0.8× 293 1.7× 111 0.8× 55 0.4× 106 0.9× 17 1.4k
Maria Assunta Chiacchio Italy 22 875 0.7× 401 2.4× 57 0.4× 97 0.7× 179 1.5× 87 1.4k
Fares Hezam Al-Ostoot India 19 489 0.4× 184 1.1× 60 0.4× 44 0.3× 98 0.8× 58 913
Nadège Lubin‐Germain France 22 838 0.6× 455 2.7× 85 0.6× 37 0.3× 71 0.6× 55 1.1k
Jay P. Parrish United States 17 515 0.4× 260 1.5× 82 0.6× 43 0.3× 43 0.4× 23 775

Countries citing papers authored by Pat Forgione

Since Specialization
Citations

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

Fields of papers citing papers by Pat Forgione

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pat Forgione

This figure shows the co-authorship network connecting the top 25 collaborators of Pat Forgione. A scholar is included among the top collaborators of Pat Forgione 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 Pat Forgione. Pat Forgione 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.
Do, Jean‐Louis, et al.. (2024). Shaking Up the Friedländer Reaction: Rapid, Scalable Mechanochemical Synthesis of Polyaryl‐Substituted Quinolines. Advanced Synthesis & Catalysis. 366(24). 5135–5143. 8 indexed citations
2.
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Forgione, Pat, et al.. (2023). Sterically‐Hindered Molecular p‐Dopants Promote Integer Charge Transfer in Organic Semiconductors. Angewandte Chemie International Edition. 62(31). e202304964–e202304964. 6 indexed citations
5.
Forgione, Pat, et al.. (2022). Efficient Synthesis of Bis(5‐arylfuran‐2‐yl)methane Scaffolds Utilizing Biomass‐Derived Starting Materials. European Journal of Organic Chemistry. 2022(8). 1 indexed citations
6.
Forgione, Pat, et al.. (2022). Decomposition of lignin models enabled by copper-based photocatalysis under biphasic conditions. Green Chemistry. 24(11). 4414–4419. 10 indexed citations
7.
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Chen, Fei, et al.. (2021). Design, structure-activity relationship study and biological evaluation of the thieno[3,2-c]isoquinoline scaffold as a potential anti-cancer agent. Bioorganic & Medicinal Chemistry Letters. 52. 128327–128327. 2 indexed citations
9.
Liang, Yanjie, et al.. (2019). Facile Aqueous-Phase Synthesis of an Ultrasmall Bismuth Nanocatalyst for the Reduction of 4-Nitrophenol. ACS Omega. 4(12). 14955–14961. 24 indexed citations
10.
Guimarães, Ana Paula de Campos, et al.. (2016). Analysis of Coxiela burnetti dihydrofolate reductase via in silico docking with inhibitors and molecular dynamics simulation. Journal of Biomolecular Structure and Dynamics. 35(13). 2975–2986. 8 indexed citations
11.
Ortgies, Dirk H., et al.. (2015). Desulfination as an Emerging Strategy in Palladium‐Catalyzed C–C Coupling Reactions. European Journal of Organic Chemistry. 2016(3). 408–425. 81 indexed citations
12.
Chen, Fei, et al.. (2014). One‐Pot Tandem Palladium‐Catalyzed Decarboxylative Cross‐Coupling and CH Activation Route to Thienoisoquinolines. Advanced Synthesis & Catalysis. 356(8). 1725–1730. 13 indexed citations
13.
Bilodeau, François, Murray D. Bailey, Josée Bordeleau, et al.. (2013). Synthesis and optimization of a novel series of HCV NS3 protease inhibitors: 4-Arylproline analogs. Bioorganic & Medicinal Chemistry Letters. 23(14). 4267–4271. 4 indexed citations
14.
Forgione, Pat, et al.. (2013). Palladium‐Catalyzed Intermolecular Desulfinylative Cross‐Coupling of Heteroaromatic Sulfinates. Chemistry - A European Journal. 19(7). 2256–2260. 33 indexed citations
15.
Forgione, Pat & Dirk H. Ortgies. (2013). A Ligand-Free Palladium-Catalyzed Cross-Coupling of Aryl Sulfinates with Aryl Bromides. Synlett. 24(13). 1715–1721. 12 indexed citations
16.
Forgione, Pat, et al.. (2012). A One-Pot Double C–H Activation Palladium Catalyzed Route to a Unique Class of Highly Functionalized Thienoisoquinolines. Organic Letters. 14(11). 2738–2741. 15 indexed citations
17.
Kawai, Stephen H., Murray D. Bailey, Ted Halmos, et al.. (2008). The Use of Chemical Double‐Mutant Cycles in Biomolecular Recognition Studies: Application to HCV NS3 Protease Inhibitors. ChemMedChem. 3(11). 1654–1657. 13 indexed citations
18.
Forgione, Pat, et al.. (2006). Unexpected Intermolecular Pd-Catalyzed Cross-Coupling Reaction Employing Heteroaromatic Carboxylic Acids as Coupling Partners. Journal of the American Chemical Society. 128(35). 11350–11351. 333 indexed citations
19.
Forgione, Pat, Peter D. Wilson, & Alex G. Fallis. (2000). Magnesium mediated carbometallation of propargyl alcohols: direct routes to furans and furanones. Tetrahedron Letters. 41(1). 17–20. 40 indexed citations
20.
Forgione, Pat, L Ferrara, & O Schettino. (1982). [The use of Eichornia crassipes for the improvement of some characteristics of water].. PubMed. 58(5). 241–5. 1 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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