A. S. Nagle

4.1k total citations
21 papers, 1.6k citations indexed

About

A. S. Nagle is a scholar working on Organic Chemistry, Molecular Biology and Public Health, Environmental and Occupational Health. According to data from OpenAlex, A. S. Nagle has authored 21 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Organic Chemistry, 9 papers in Molecular Biology and 6 papers in Public Health, Environmental and Occupational Health. Recurrent topics in A. S. Nagle's work include Chemical Synthesis and Reactions (6 papers), Chemical Synthesis and Analysis (5 papers) and Asymmetric Hydrogenation and Catalysis (5 papers). A. S. Nagle is often cited by papers focused on Chemical Synthesis and Reactions (6 papers), Chemical Synthesis and Analysis (5 papers) and Asymmetric Hydrogenation and Catalysis (5 papers). A. S. Nagle collaborates with scholars based in United States, United Kingdom and Switzerland. A. S. Nagle's co-authors include Kyung Woon Jung, Ralph Nicholas Salvatore, Nathanael S. Gray, Arnab K. Chatterjee, Valentina Molteni, František Supek, Frederick S. Buckner, Nagendar Pendem, Francisco Adrián and Michael H. Gelb and has published in prestigious journals such as Chemical Reviews, Proceedings of the National Academy of Sciences and Journal of Medicinal Chemistry.

In The Last Decade

A. S. Nagle

21 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
A. S. Nagle United States 17 831 498 468 245 234 21 1.6k
Luiz C. Dias Brazil 25 1.9k 2.2× 218 0.4× 665 1.4× 243 1.0× 186 0.8× 132 2.7k
Kelly Chibale South Africa 28 1.3k 1.6× 265 0.5× 442 0.9× 87 0.4× 106 0.5× 49 1.8k
Marco Radi Italy 29 1.4k 1.7× 146 0.3× 981 2.1× 123 0.5× 55 0.2× 97 2.5k
Xinhong Yu China 21 1.8k 2.2× 139 0.3× 642 1.4× 420 1.7× 439 1.9× 57 3.0k
Rebecca Deprez‐Poulain France 24 941 1.1× 164 0.3× 733 1.6× 155 0.6× 36 0.2× 61 1.7k
Richard Angell United Kingdom 17 293 0.4× 23 0.0× 403 0.9× 56 0.2× 63 0.3× 31 860
Alice Dawson United Kingdom 19 597 0.7× 75 0.2× 454 1.0× 91 0.4× 235 1.0× 38 1.5k
Alejandro Álvarez‐Hernández Mexico 15 444 0.5× 116 0.2× 123 0.3× 67 0.3× 43 0.2× 36 751
Amy Barrios United States 25 487 0.6× 90 0.2× 956 2.0× 80 0.3× 331 1.4× 61 2.1k
Swarna A. Gamage New Zealand 20 830 1.0× 112 0.2× 912 1.9× 56 0.2× 57 0.2× 39 1.7k

Countries citing papers authored by A. S. Nagle

Since Specialization
Citations

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

Fields of papers citing papers by A. S. Nagle

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A. S. Nagle. 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 A. S. Nagle. The network helps show where A. S. Nagle may publish in the future.

Co-authorship network of co-authors of A. S. Nagle

This figure shows the co-authorship network connecting the top 25 collaborators of A. S. Nagle. A scholar is included among the top collaborators of A. S. Nagle 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 A. S. Nagle. A. S. Nagle 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.
Nagle, A. S., Shilpi Khare, Arun Kumar, et al.. (2014). Recent Developments in Drug Discovery for Leishmaniasis and Human African Trypanosomiasis. Chemical Reviews. 114(22). 11305–11347. 266 indexed citations
2.
Gillespie, J. Robert, Arnab K. Chatterjee, Neil R. Norcross, et al.. (2013). Substituted 2-Phenylimidazopyridines: A New Class of Drug Leads for Human African Trypanosomiasis. Journal of Medicinal Chemistry. 57(3). 828–835. 57 indexed citations
3.
Wu, Tao, A. S. Nagle, & Arnab K. Chatterjee. (2011). Road Towards New Antimalarials – Overview of the Strategies and their Chemical Progress. Current Medicinal Chemistry. 18(6). 853–871. 29 indexed citations
4.
Deng, Xianming, A. S. Nagle, Tao Wu, et al.. (2010). Discovery of novel 1H-imidazol-2-yl-pyrimidine-4,6-diamines as potential antimalarials. Bioorganic & Medicinal Chemistry Letters. 20(14). 4027–4031. 18 indexed citations
5.
Wu, Tao, A. S. Nagle, Tomoyo Sakata, et al.. (2009). Cell-based optimization of novel benzamides as potential antimalarial leads. Bioorganic & Medicinal Chemistry Letters. 19(24). 6970–6974. 11 indexed citations
6.
Park, Chan Pil, et al.. (2009). Formal Aromatic C−H Insertion for Stereoselective Isoquinolinone Synthesis and Studies on Mechanistic Insights into the C−C Bond Formation. The Journal of Organic Chemistry. 74(16). 6231–6236. 53 indexed citations
7.
Plouffe, David, Achim Brinker, Case W. McNamara, et al.. (2008). In silico activity profiling reveals the mechanism of action of antimalarials discovered in a high-throughput screen. Proceedings of the National Academy of Sciences. 105(26). 9059–9064. 325 indexed citations
8.
Hur, Wooyoung, Anastasia Velentza, Sung Joon Kim, et al.. (2008). Clinical stage EGFR inhibitors irreversibly alkylate Bmx kinase. Bioorganic & Medicinal Chemistry Letters. 18(22). 5916–5919. 32 indexed citations
9.
Barun, Okram, A. S. Nagle, Francisco Adrián, et al.. (2006). A General Strategy for Creating “Inactive-Conformation” Abl Inhibitors. Chemistry & Biology. 13(7). 779–786. 124 indexed citations
10.
Nagle, A. S., Wooyoung Hur, & Nathanael S. Gray. (2006). Antimitotic Agents of Natural Origin. Current Drug Targets. 7(3). 305–326. 54 indexed citations
11.
Jung, Kyung Woon & A. S. Nagle. (2005). Acyclic and Cyclic Carbonic Acids and Esters, and Their Sulfur, Selenium, and Tellurium Analogues. ChemInform. 36(38). 1 indexed citations
12.
Miller, Laura A., Mitchell A. deLong, Lamar Galloway, et al.. (2003). Glutathione, S-substituted glutathiones, and leukotriene C4 as substrates for peptidylglycine α-amidating monooxygenase. Archives of Biochemistry and Biophysics. 412(1). 3–12. 7 indexed citations
14.
Nagle, A. S., et al.. (2003). Selective mono protection of diols, diamines, and amino alcohols using cesium bases. Tetrahedron Letters. 44(30). 5695–5698. 17 indexed citations
15.
Salvatore, Ralph Nicholas, A. S. Nagle, & Kyung Woon Jung. (2002). Cesium Effect:  High Chemoselectivity in Direct N-Alkylation of Amines. The Journal of Organic Chemistry. 67(3). 674–683. 219 indexed citations
16.
Salvatore, Ralph Nicholas, et al.. (2002). Efficient Cs2CO3-promoted solution and solid phase synthesis of carbonates and carbamates in the presence of TBAI. Tetrahedron. 58(17). 3329–3347. 58 indexed citations
17.
Salvatore, Ralph Nicholas, et al.. (2001). Efficient Carbamate Synthesis via a Three-Component Coupling of an Amine, CO2, and Alkyl Halides in the Presence of Cs2CO3 and Tetrabutylammonium Iodide. The Journal of Organic Chemistry. 66(3). 1035–1037. 146 indexed citations
18.
Salvatore, Ralph Nicholas, et al.. (2000). CsOH-promoted chemoselective mono-N-alkylation of diamines and polyamines. Tetrahedron Letters. 41(50). 9705–9708. 22 indexed citations
19.
Nagle, A. S., et al.. (2000). Efficient synthesis of β-amino bromides. Tetrahedron Letters. 41(17). 3011–3014. 34 indexed citations
20.
Salvatore, Ralph Nicholas, et al.. (1999). Cesium Hydroxide Promoted Chemoselective N-Alkylation for the Generally Efficient Synthesis of Secondary Amines. Organic Letters. 1(12). 1893–1896. 76 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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