Thomas M. Bargar

577 total citations
19 papers, 432 citations indexed

About

Thomas M. Bargar is a scholar working on Organic Chemistry, Cardiology and Cardiovascular Medicine and Plant Science. According to data from OpenAlex, Thomas M. Bargar has authored 19 papers receiving a total of 432 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Organic Chemistry, 3 papers in Cardiology and Cardiovascular Medicine and 3 papers in Plant Science. Recurrent topics in Thomas M. Bargar's work include Synthesis of heterocyclic compounds (3 papers), Sulfur-Based Synthesis Techniques (3 papers) and Catalytic Cross-Coupling Reactions (2 papers). Thomas M. Bargar is often cited by papers focused on Synthesis of heterocyclic compounds (3 papers), Sulfur-Based Synthesis Techniques (3 papers) and Catalytic Cross-Coupling Reactions (2 papers). Thomas M. Bargar collaborates with scholars based in United States, China and Netherlands. Thomas M. Bargar's co-authors include M. F. SEMMELHACK, George R. Clark, H. Tracy Hall, K. Hirotsu, Masaaki Yoshifuji, Jon Clardy, Christopher M. Riley, James R. McCarthy, Michael T. Kenny and Lawrence C. Creemer and has published in prestigious journals such as Journal of the American Chemical Society, Journal of Agricultural and Food Chemistry and Journal of Medicinal Chemistry.

In The Last Decade

Thomas M. Bargar

19 papers receiving 394 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas M. Bargar United States 12 344 91 64 35 29 19 432
Jean-Paul G. Seerden Netherlands 12 386 1.1× 170 1.9× 46 0.7× 28 0.8× 35 1.2× 13 531
Masaru Ogata Japan 14 394 1.1× 92 1.0× 23 0.4× 4 0.1× 29 1.0× 51 498
D. T. CONNOR United States 8 375 1.1× 111 1.2× 20 0.3× 7 0.2× 12 0.4× 23 517
Р. Г. Глушков Bulgaria 9 195 0.6× 90 1.0× 11 0.2× 18 0.5× 16 0.6× 110 360
Satoshi Tamai Japan 13 302 0.9× 172 1.9× 41 0.6× 7 0.2× 14 0.5× 32 453
Iana Vazzana Italy 10 288 0.8× 84 0.9× 14 0.2× 18 0.5× 5 0.2× 18 361
Gültaze Çapan Türkiye 12 471 1.4× 108 1.2× 40 0.6× 6 0.2× 14 0.5× 24 541
C Luu-Duc France 10 285 0.8× 140 1.5× 22 0.3× 6 0.2× 31 1.1× 65 395
Willy Logemann Italy 11 172 0.5× 97 1.1× 20 0.3× 6 0.2× 21 0.7× 52 319
Katherine Rielly-Gauvin United States 6 529 1.5× 121 1.3× 207 3.2× 10 0.3× 63 2.2× 6 570

Countries citing papers authored by Thomas M. Bargar

Since Specialization
Citations

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

Fields of papers citing papers by Thomas M. Bargar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas M. Bargar

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

All Works

19 of 19 papers shown
1.
Qian, Lijun, John Lof, Thomas M. Bargar, et al.. (2021). Delayed Echo Enhancement Imaging to Quantify Myocardial Infarct Size. Journal of the American Society of Echocardiography. 34(8). 898–909. 4 indexed citations
2.
Bargar, Thomas M., et al.. (1997). Inhibition of nematode induced root damage by derivatives of methylenecyclopropane acetic acid. Bioorganic & Medicinal Chemistry Letters. 7(20). 2665–2668. 12 indexed citations
3.
Bargar, Thomas M., et al.. (1995). Toxicity of Pumiliotoxin 251D and Synthetic Analogs to the Cotton Pest Heliothis virescens. Journal of Agricultural and Food Chemistry. 43(4). 1044–1051. 21 indexed citations
4.
Bargar, Thomas M., Robert J. Broersma, Lawrence C. Creemer, et al.. (1988). Highly effective mechanism-based inactivation of dopamine .beta.-hydroxylase by a novel ketene thioacetal. Journal of the American Chemical Society. 110(9). 2975–2976. 4 indexed citations
5.
Creemer, Lawrence C., et al.. (1988). A Convenient Synthesis of β,β-Bis(Alkylthio)Acrylonitriles. Synthetic Communications. 18(10). 1103–1110. 3 indexed citations
6.
Bargar, Thomas M., et al.. (1987). Stabase-protected 2-chloroallylamine: a useful synthon for primary allylic amines via nickel-catalyzed cross-coupling. The Journal of Organic Chemistry. 52(4). 678–681. 12 indexed citations
7.
McCarthy, James R., et al.. (1987). A facile synthesis of β-substituted-α-allenyl primary amines. Tetrahedron Letters. 28(20). 2207–2210. 10 indexed citations
8.
Kenny, Michael T., et al.. (1987). Antipicornavirus activity of some diaryl methanes and aralkylaminopyridines. Antiviral Research. 7(2). 87–97. 8 indexed citations
9.
Markley, Lowell D., et al.. (1986). Antipicornavirus activity of substituted phenoxybenzenes and phenoxypyridines. Journal of Medicinal Chemistry. 29(3). 427–433. 28 indexed citations
10.
Bargar, Thomas M., Robert J. Broersma, Lawrence C. Creemer, et al.. (1986). Unsaturated heterocyclic amines as potent time-dependent inhibitors of dopamine .beta.-hydroxylase. Journal of Medicinal Chemistry. 29(3). 315–317. 39 indexed citations
11.
Bargar, Thomas M., et al.. (1986). 3,4-Dihydro-2-phenyl-2H-pyrano[2,3-b]pyridines with potent antirhinovirus activity. Journal of Medicinal Chemistry. 29(9). 1590–1595. 13 indexed citations
12.
Kenny, Michael T., et al.. (1986). In vitro antiviral activity of the 6-substituted 2-(3',4'-dichlorophenoxy)-2H-pyrano[2,3-b]pyridines MDL 20,610, MDL 20,646, and MDL 20,957. Antimicrobial Agents and Chemotherapy. 30(3). 516–518. 16 indexed citations
13.
Bargar, Thomas M., et al.. (1985). 3,4‐Dihydro‐2‐phenyl‐2H‐pyrano[2,3‐b]pyridines. Novel aza analogs of flavans. Journal of Heterocyclic Chemistry. 22(6). 1583–1592. 8 indexed citations
14.
Bargar, Thomas M., et al.. (1984). Synthesis of 9,10,11,12,12a,13‐hexahydro‐2,3‐dimethoxy‐7H‐naphtho[l, 2‐b]quinolizine hydrobromide. A cell growth inhibitor related to cryptopleurine. Journal of Heterocyclic Chemistry. 21(1). 261–263. 2 indexed citations
15.
Bargar, Thomas M. & Christopher M. Riley. (1980). A Rapid and Efficient Method for Dehydration of Primary Amides to Nitriles. Preparation of Acrylonitrile Derivatives. Synthetic Communications. 10(6). 479–487. 29 indexed citations
16.
SEMMELHACK, M. F. & Thomas M. Bargar. (1980). Photostimulated nucleophilic aromatic substitution for halides with carbon nucleophiles. Preparative and mechanistic aspects. Journal of the American Chemical Society. 102(26). 7765–7774. 54 indexed citations
17.
SEMMELHACK, M. F., H. Tracy Hall, Masaaki Yoshifuji, et al.. (1979). .eta.5-Cyclohexadienyltricarbonylchromium(0) complexes from addition of carbon nucleophiles to .eta.6-benzenetricarbonylchromium(0). Formation, chemical and spectroscopic features, and x-ray diffraction analysis. Journal of the American Chemical Society. 101(13). 3535–3544. 119 indexed citations
18.
SEMMELHACK, M. F. & Thomas M. Bargar. (1977). Cyclizations of enolates onto aromatic rings via the photo-SRN1 reaction. Preparative and mechanistic aspects. The Journal of Organic Chemistry. 42(8). 1481–1482. 32 indexed citations
19.
Bargar, Thomas M., et al.. (1976). Correction. Transfer of Oxygen to Organic Sulfides with Dimethyl Sulfoxide Catalyzed by Hydrogen Chloride. Preparation of Disulfoxides. The Journal of Organic Chemistry. 41(25). 4051–4051. 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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