Paul M. Scola

2.2k total citations
33 papers, 1.4k citations indexed

About

Paul M. Scola is a scholar working on Organic Chemistry, Molecular Biology and Hepatology. According to data from OpenAlex, Paul M. Scola has authored 33 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Organic Chemistry, 10 papers in Molecular Biology and 8 papers in Hepatology. Recurrent topics in Paul M. Scola's work include Hepatitis C virus research (8 papers), HIV/AIDS drug development and treatment (7 papers) and Chemical Synthesis and Analysis (6 papers). Paul M. Scola is often cited by papers focused on Hepatitis C virus research (8 papers), HIV/AIDS drug development and treatment (7 papers) and Chemical Synthesis and Analysis (6 papers). Paul M. Scola collaborates with scholars based in United States, Germany and Sweden. Paul M. Scola's co-authors include Steven M. Weinreb, Francis G. Fang, Yoshito Kishi, Keith R. Buszek, Craig J. Forsyth, Thomas D. Aicher, Sun Ho Jung, James R. Henry, Matthias C. McIntosh and Georgianna Harris and has published in prestigious journals such as Chemical Reviews, Journal of the American Chemical Society and Angewandte Chemie International Edition.

In The Last Decade

Paul M. Scola

32 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Paul M. Scola United States 17 1.0k 417 176 146 142 33 1.4k
Hans Maag United States 15 525 0.5× 448 1.1× 74 0.4× 50 0.3× 53 0.4× 22 986
Benoı̂t Joseph France 25 1.6k 1.5× 822 2.0× 126 0.7× 50 0.3× 16 0.1× 95 2.3k
Zhu‐Jun Yao China 25 1.3k 1.2× 634 1.5× 193 1.1× 67 0.5× 39 0.3× 96 1.8k
Tony Raynham United Kingdom 20 554 0.5× 410 1.0× 61 0.3× 27 0.2× 44 0.3× 34 866
Oliver Simić Switzerland 14 534 0.5× 196 0.5× 41 0.2× 87 0.6× 34 0.2× 16 727
Kaapjoo Park United States 19 372 0.4× 244 0.6× 71 0.4× 40 0.3× 73 0.5× 25 693
Jean‐Louis Kraus France 18 453 0.4× 407 1.0× 138 0.8× 22 0.2× 19 0.1× 73 996
Zhi‐Jie Ni United States 20 700 0.7× 399 1.0× 49 0.3× 10 0.1× 96 0.7× 37 1.1k
J. Brad Shotwell United States 16 412 0.4× 241 0.6× 55 0.3× 52 0.4× 23 0.2× 27 714
Lee Funk United States 6 1.3k 1.2× 389 0.9× 48 0.3× 12 0.1× 33 0.2× 7 1.6k

Countries citing papers authored by Paul M. Scola

Since Specialization
Citations

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

Fields of papers citing papers by Paul M. Scola

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Paul M. Scola. 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 Paul M. Scola. The network helps show where Paul M. Scola may publish in the future.

Co-authorship network of co-authors of Paul M. Scola

This figure shows the co-authorship network connecting the top 25 collaborators of Paul M. Scola. A scholar is included among the top collaborators of Paul M. Scola 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 Paul M. Scola. Paul M. Scola 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.
Strauss, Michael J., Jakob C. Dahl, Seoung‐Tae Kim, et al.. (2024). Cu-Catalyzed Amination of Base-Sensitive Aryl Bromides and the Chemoselective N- and O-Arylation of Amino Alcohols. Journal of the American Chemical Society. 146(27). 18616–18625. 23 indexed citations
2.
Strauss, Michael J., Seoung‐Tae Kim, Christiana N. Teijaro, et al.. (2024). Room‐Temperature Copper‐Catalyzed Etherification of Aryl Bromides. Angewandte Chemie International Edition. 63(19). e202400333–e202400333. 19 indexed citations
3.
Moon, Hye Won, Marissa N. Lavagnino, Maximilian D. Palkowitz, et al.. (2023). Deoxyfluorination of 1°, 2°, and 3° Alcohols by Nonbasic O–H Activation and Lewis Acid-Catalyzed Fluoride Shuttling. Journal of the American Chemical Society. 145(41). 22735–22744. 13 indexed citations
4.
Donnelly, David J., Yunhui Zhang, Paul M. Scola, et al.. (2023). Development, Characterization, and Radiation Dosimetry Studies of 18F-BMS-986229, a 18F-Labeled PD-L1 Macrocyclic Peptide PET Tracer. Molecular Imaging and Biology. 26(2). 301–309. 3 indexed citations
5.
Donnelly, David J., Joon‐Young Kim, Paul M. Scola, et al.. (2023). The discovery and evaluation of [18F]BMS-986229, a novel macrocyclic peptide PET radioligand for the measurement of PD-L1 expression and in-vivo PD-L1 target engagement. European Journal of Nuclear Medicine and Molecular Imaging. 51(4). 978–990. 13 indexed citations
6.
Ni, Shengyang, Alberto F. Garrido‐Castro, Rohan R. Merchant, et al.. (2018). A General Amino Acid Synthesis Enabled by Innate Radical Cross‐Coupling. Angewandte Chemie International Edition. 57(44). 14560–14565. 116 indexed citations
7.
Hiebert, Sheldon, Jacques Friborg, Fei Yu, et al.. (2017). The discovery and optimization of naphthalene-linked P2-P4 Macrocycles as inhibitors of HCV NS3 protease. Bioorganic & Medicinal Chemistry Letters. 28(1). 43–48. 8 indexed citations
8.
Malins, Lara R., Justine N. deGruyter, Kevin J. Robbins, et al.. (2017). Peptide Macrocyclization Inspired by Non-Ribosomal Imine Natural Products. Journal of the American Chemical Society. 139(14). 5233–5241. 106 indexed citations
9.
Chen, Jie, Qian Zhao, Li‐Qiang Sun, et al.. (2016). Structure-activity relationships of 4-hydroxy-4-biaryl-proline acylsulfonamide tripeptides: A series of potent NS3 protease inhibitors for the treatment of hepatitis C virus. Bioorganic & Medicinal Chemistry Letters. 27(3). 590–596. 5 indexed citations
10.
Sun, Li‐Qiang, Qian Zhao, Betsy J. Eggers, et al.. (2016). Functionalized triazines as potent HCV entry inhibitors. Bioorganic & Medicinal Chemistry Letters. 27(4). 1089–1093. 3 indexed citations
11.
Chen, Gang, Pankaj Jain, Zhipeng Zhang, et al.. (2015). Ligand-Enabled β-C–H Arylation of α-Amino Acids Using a Simple and Practical Auxiliary. Journal of the American Chemical Society. 137(9). 3338–3351. 150 indexed citations
12.
Mosure, Kathleen, Jay O. Knipe, Vinod Arora, et al.. (2015). Preclinical Pharmacokinetics and In Vitro Metabolism of Asunaprevir (BMS-650032), a Potent Hepatitis C Virus NS3 Protease Inhibitor. Journal of Pharmaceutical Sciences. 104(9). 2813–2823. 27 indexed citations
13.
Hu, Shuanghua, Yong‐Jin Wu, Huan He, et al.. (2014). Structure activity relationship studies of 3-arylsulfonyl-pyrido[1,2-a]pyrimidin-4-imines as potent 5-HT6 antagonists. Bioorganic & Medicinal Chemistry. 22(5). 1782–1790. 17 indexed citations
14.
McPhee, Fiona, Amy K. Sheaffer, Jacques Friborg, et al.. (2012). Preclinical Profile and Characterization of the Hepatitis C Virus NS3 Protease Inhibitor Asunaprevir (BMS-650032). Antimicrobial Agents and Chemotherapy. 56(10). 5387–5396. 139 indexed citations
15.
16.
Li, Jianqing, et al.. (2006). A Facile Synthesis of 1-Substituted Cyclopropylsulfonamides. Synlett. 725–728. 8 indexed citations
17.
Meanwell, Nicholas A., Makonen Belema, David J. Carini, et al.. (2005). Developments in Antiviral Drug Design, Discovery and Development in 2004. PubMed. 5(4). 307–400. 4 indexed citations
18.
Dubowchik, Gene M., Dmitry Zuev, Paul M. Scola, et al.. (2003). 2-Arylaminothiazoles as high-affinity corticotropin-Releasing factor 1 receptor (CRF1R) antagonists: synthesis, binding studies and behavioral efficacy. Bioorganic & Medicinal Chemistry Letters. 13(22). 3997–4000. 14 indexed citations
19.
Weinreb, Steven M., et al.. (1996). An Attempted Total Synthesis of Lysergic Acid via an Alkene/N-Sulfonylimine Cyclization. Heterocycles. 43(7). 1497–1497. 9 indexed citations
20.
Fang, Francis G., et al.. (1992). Synthetic Studies Towards Halichondrins: Synthesis of the Left Halves of Norhalichondrins and Homohalichondrins. Tetrahedron Letters. 33(12). 1557–1560. 18 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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