David M. Stout

1.3k total citations · 1 hit paper
19 papers, 1.1k citations indexed

About

David M. Stout is a scholar working on Organic Chemistry, Molecular Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, David M. Stout has authored 19 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Organic Chemistry, 4 papers in Molecular Biology and 2 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in David M. Stout's work include Chemical Reaction Mechanisms (4 papers), Bioactive Compounds and Antitumor Agents (2 papers) and Computational Drug Discovery Methods (2 papers). David M. Stout is often cited by papers focused on Chemical Reaction Mechanisms (4 papers), Bioactive Compounds and Antitumor Agents (2 papers) and Computational Drug Discovery Methods (2 papers). David M. Stout collaborates with scholars based in United States, China and Canada. David M. Stout's co-authors include A. I. MEYERS, W. L. Matier, Lawrence A. Black, Barry S. Brown, TAKAO TAKAYA, Robert D. Reynolds, Nanjie Deng, Peng He, Ramachandran Vijayan and Lauren Wickstrom and has published in prestigious journals such as Chemical Reviews, The Journal of Physical Chemistry B and Journal of Medicinal Chemistry.

In The Last Decade

David M. Stout

19 papers receiving 1.1k citations

Hit Papers

Recent advances in the chemistry of dihydropyridines 1982 2026 1996 2011 1982 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David M. Stout United States 11 893 286 146 67 62 19 1.1k
Ian A. O’Neil United Kingdom 18 687 0.8× 372 1.3× 72 0.5× 81 1.2× 44 0.7× 67 984
Naresh K. Nayyar United States 16 1.3k 1.4× 289 1.0× 214 1.5× 93 1.4× 54 0.9× 30 1.4k
Bruno Schönecker Germany 17 589 0.7× 369 1.3× 248 1.7× 59 0.9× 69 1.1× 80 978
F. E. ROBERTS United States 12 556 0.6× 244 0.9× 169 1.2× 76 1.1× 64 1.0× 25 786
Wen‐Chung Shieh United States 16 726 0.8× 272 1.0× 178 1.2× 30 0.4× 45 0.7× 34 939
Chung‐Mao Pan United States 10 1.2k 1.4× 341 1.2× 244 1.7× 69 1.0× 25 0.4× 12 1.5k
F.B. Kaynak Türkiye 15 844 0.9× 358 1.3× 296 2.0× 76 1.1× 96 1.5× 44 1.2k
Ante Nagl Croatia 16 583 0.7× 217 0.8× 127 0.9× 98 1.5× 71 1.1× 80 836
William S. Mungall United States 11 633 0.7× 347 1.2× 160 1.1× 81 1.2× 125 2.0× 17 983
Edward B. Skibo United States 23 1.2k 1.3× 599 2.1× 65 0.4× 41 0.6× 37 0.6× 66 1.5k

Countries citing papers authored by David M. Stout

Since Specialization
Citations

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

Fields of papers citing papers by David M. Stout

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David M. Stout

This figure shows the co-authorship network connecting the top 25 collaborators of David M. Stout. A scholar is included among the top collaborators of David M. Stout 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 M. Stout. David M. Stout 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
2.
Deng, Nanjie, Stefano Forli, Peng He, et al.. (2014). Distinguishing Binders from False Positives by Free Energy Calculations: Fragment Screening Against the Flap Site of HIV Protease. The Journal of Physical Chemistry B. 119(3). 976–988. 55 indexed citations
3.
Liu, Yinhui, Hongmei Wang, Hao Wu, et al.. (2009). Design, synthesis, and evaluation of novel 3-amino-4-hydrazine-cyclobut-3-ene-1,2-diones as potent and selective CXCR2 chemokine receptor antagonists. Bioorganic & Medicinal Chemistry Letters. 19(19). 5741–5745. 13 indexed citations
4.
Clement, Stephen L., Terry Griswold, Richard W. Rust, Barbara Hellier, & David M. Stout. (2006). Bee Associates of Flowering Astragalus and Onobrychis Genebank Accessions at a Snake River Site in Eastern Washington. Journal of the Kansas Entomological Society. 79(3). 254–260. 11 indexed citations
5.
Reddy, N. Laxma, Jeanette R. Hill, Long Ye, Prabhavathi Fernandes, & David M. Stout. (2004). Identification and structure–activity relationship studies of 3-methylene-2-norbornanone as potent anti-proliferative agents presumably working through p53 mediated apoptosis. Bioorganic & Medicinal Chemistry Letters. 14(22). 5645–5649. 10 indexed citations
6.
Meyer, Michael D., Arthur A. Hancock, Karin Tietje, et al.. (1997). Structure−Activity Studies for a Novel Series ofN-(Arylethyl)-N-(1,2,3,4-tetrahydronaphthalen-1-ylmethyl)-N-methylamines Possessing Dual 5-HT Uptake Inhibiting and α2-Antagonistic Activities. Journal of Medicinal Chemistry. 40(7). 1049–1062. 29 indexed citations
7.
Chorvat, Robert J., Lawrence A. Black, Vasant Ranade, et al.. (1993). Mono- and bis(aminomethyl)phenylacetic acid esters as short-acting antiarrhythmic agents. 2. Journal of Medicinal Chemistry. 36(17). 2494–2498. 5 indexed citations
8.
Stout, David M., Lawrence A. Black, W. L. Matier, et al.. (1989). Ester derivatives of 2,6-bis(1-pyrrolidinylmethyl)-4-benzamidophenol as short-acting antiarrhythmic agents. 1. Journal of Medicinal Chemistry. 32(8). 1910–1913. 5 indexed citations
9.
Stout, David M., et al.. (1985). Synthesis and antiarrhythmic and parasympatholytic properties of substituted phenols. 3. Modifications to the linkage region (region 3). Journal of Medicinal Chemistry. 28(3). 295–298. 23 indexed citations
10.
Stout, David M., et al.. (1984). Synthesis and antiarrhythmic and parasympatholytic properties of substituted phenols. 2. Amides. Journal of Medicinal Chemistry. 27(10). 1347–1350. 10 indexed citations
11.
Stout, David M., Lawrence A. Black, & W. L. Matier. (1983). Asymmetric Strecker synthesis: isolation of pure enantiomers and mechanistic implications. The Journal of Organic Chemistry. 48(26). 5369–5373. 57 indexed citations
12.
Stout, David M., et al.. (1983). Synthesis and antiarrhythmic and parasympatholytic properties of substituted phenols. 1. Heteroarylamine derivatives. Journal of Medicinal Chemistry. 26(6). 808–813. 18 indexed citations
13.
Stout, David M. & A. I. MEYERS. (1982). Recent advances in the chemistry of dihydropyridines. Chemical Reviews. 82(2). 223–243. 810 indexed citations breakdown →
14.
Stout, David M. & Richard J. Gorczynski. (1982). N-Aralkyl substitution of 2-amino-5,6- and -6,7-dihydroxy-1,2,3,4-tetrahydronaphthalenes. 2. Derivatives of a hypotensive-positive inotropic agent. Journal of Medicinal Chemistry. 25(3). 326–328. 6 indexed citations
15.
Gorczynski, Richard J., W. Gary Anderson, & David M. Stout. (1981). N-Aralkyl substitution of 2-amino-5,6- and -6,7-dihydroxy-1,2,3,4-tetrahydronaphthalenes. 1. Cardiac and pressor/depressor activities. Journal of Medicinal Chemistry. 24(7). 835–839. 7 indexed citations
16.
Friedrich, Louis E., et al.. (1980). Conformational control of oxabicyclobutane fragmentations. The Journal of Organic Chemistry. 45(16). 3198–3202. 2 indexed citations
17.
Friedrich, Louis E., et al.. (1978). Synthesis and epoxidation kinetics of some fused-ring cyclopropenes. The Journal of Organic Chemistry. 43(4). 604–610. 9 indexed citations
18.
Stout, David M., TAKAO TAKAYA, & A. I. MEYERS. (1975). Unequivocal synthesis of N-substituted 1,4-dihydropyridines. The Journal of Organic Chemistry. 40(5). 563–569. 31 indexed citations
19.
MEYERS, A. I., David M. Stout, & TAKAO TAKAYA. (1972). Nuclear synthesis of 1,4-dihydropyridines by rearrangement of aziridinobicyclo[2,2,1]pyridazine carboxylates. Journal of the Chemical Society Chemical Communications. 1260–1260. 4 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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