David E. Minter

741 total citations
39 papers, 572 citations indexed

About

David E. Minter is a scholar working on Organic Chemistry, Molecular Biology and Physical and Theoretical Chemistry. According to data from OpenAlex, David E. Minter has authored 39 papers receiving a total of 572 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Organic Chemistry, 12 papers in Molecular Biology and 6 papers in Physical and Theoretical Chemistry. Recurrent topics in David E. Minter's work include Asymmetric Synthesis and Catalysis (8 papers), Natural product bioactivities and synthesis (4 papers) and Analytical Chemistry and Chromatography (3 papers). David E. Minter is often cited by papers focused on Asymmetric Synthesis and Catalysis (8 papers), Natural product bioactivities and synthesis (4 papers) and Analytical Chemistry and Chromatography (3 papers). David E. Minter collaborates with scholars based in United States, Egypt and Pakistan. David E. Minter's co-authors include Myron K. Jacobson, Elaine L. Jacobson, Daniel Cervantes-Laurean, Qi Jia, Srinivasa Nalabolu, Paul Cook, Manfred G. Reinecke, Philip L. Stotter, Gerhard J. Fonken and Hong Qi and has published in prestigious journals such as Journal of the American Chemical Society, Journal of Biological Chemistry and Biochemistry.

In The Last Decade

David E. Minter

38 papers receiving 543 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David E. Minter United States 14 228 181 89 85 63 39 572
Md Arshad India 15 280 1.2× 238 1.3× 82 0.9× 89 1.0× 10 0.2× 36 738
Hidetaka Yuki Japan 14 272 1.2× 175 1.0× 18 0.2× 42 0.5× 14 0.2× 83 638
Dušan Miljković Serbia 15 240 1.1× 275 1.5× 29 0.3× 52 0.6× 30 0.5× 57 588
Аndrey G. Pokrovsky Russia 18 411 1.8× 292 1.6× 49 0.6× 64 0.8× 9 0.1× 78 835
Barbara Gerratana United States 16 475 2.1× 226 1.2× 63 0.7× 33 0.4× 6 0.1× 23 712
S. D. GÉRO France 20 493 2.2× 759 4.2× 37 0.4× 267 3.1× 14 0.2× 92 1.3k
M.J. Alcaraz Spain 12 180 0.8× 187 1.0× 29 0.3× 58 0.7× 6 0.1× 17 573
T. Barna United Kingdom 15 380 1.7× 124 0.7× 70 0.8× 156 1.8× 14 0.2× 24 740
Tomohisa Nagamatsu Japan 17 490 2.1× 643 3.6× 40 0.4× 332 3.9× 18 0.3× 100 1.3k
Donna B. Cosulich United States 14 347 1.5× 375 2.1× 66 0.7× 24 0.3× 37 0.6× 25 768

Countries citing papers authored by David E. Minter

Since Specialization
Citations

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

Fields of papers citing papers by David E. Minter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David E. Minter

This figure shows the co-authorship network connecting the top 25 collaborators of David E. Minter. A scholar is included among the top collaborators of David E. Minter 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 E. Minter. David E. Minter 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.
Qi, Hong, et al.. (2010). Anti-tuberculosis Compounds from Mallotus philippinensis. Natural Product Communications. 5(2). 211–7. 16 indexed citations
2.
Nesterov, Alexandre, Jifu Zhao, David E. Minter, et al.. (2008). 1-(2,4-Dihydroxyphenyl)-3-(2,4-dimethoxy-3-methylphenyl)propane, a Novel Tyrosinase Inhibitor with Strong Depigmenting Effects. Chemical and Pharmaceutical Bulletin. 56(9). 1292–1296. 33 indexed citations
3.
Qi, Hong, David E. Minter, Scott G. Franzblau, & Manfred G. Reinecke. (2008). Anti-tuberculosis Compounds from two Bolivian Medicinal Plants, Senecio Mathewsii and Usnea Florida. Natural Product Communications. 3(9). 13 indexed citations
4.
Minter, David E., et al.. (2006). Structure elucidation of an unexpected product from dehydration of a β‐hydroxyketone. Magnetic Resonance in Chemistry. 44(10). 969–971. 1 indexed citations
5.
Minter, David E., et al.. (2004). A Photochemical Approach to the Galanthan Ring System. The Journal of Organic Chemistry. 69(5). 1603–1606. 22 indexed citations
6.
Minter, David E., et al.. (2002). NMR analyses of two isomeric cyclobutanes from a [2 + 2] photocycloaddition. Magnetic Resonance in Chemistry. 40(6). 412–414. 5 indexed citations
7.
Cervantes-Laurean, Daniel, Paul T. Loflin, David E. Minter, Elaine L. Jacobson, & Myron K. Jacobson. (1995). Protein Modification by ADP-ribose via Acid-labile Linkages. Journal of Biological Chemistry. 270(14). 7929–7936. 30 indexed citations
8.
Reinecke, Manfred G., David E. Minter, & Qi Jia. (1995). Carbon and proton NMR assignments for 6,7‐dimethoxycoumarin. Magnetic Resonance in Chemistry. 33(9). 757–758. 5 indexed citations
9.
10.
Cervantes-Laurean, Daniel, David E. Minter, Elaine L. Jacobson, & Myron K. Jacobson. (1993). Protein glycation by ADP-ribose: Studies of model conjugates. Biochemistry. 32(6). 1528–1534. 89 indexed citations
11.
Reinecke, Manfred G., et al.. (1988). 3,4-Didehydropyridine plus cyclopentadiene: [2+2] or [4+2]-cycloaddition ?. Tetrahedron. 44(18). 5675–5680. 8 indexed citations
12.
Stotter, Philip L., et al.. (1987). Quinuclidine∑boranes as Intermediates in Formation and Isolation of Functionalized Quinuclidine Systems. Heterocycles. 25(1). 251–251. 17 indexed citations
13.
Minter, David E., Curtis R. Kelly, & Henry C. Kelly. (1986). Substituent effects in the hydrolysis of quinoline-boranes. Inorganic Chemistry. 25(18). 3291–3294. 5 indexed citations
14.
Minter, David E., et al.. (1985). The esterification of trifluoroacetic acid: An NMR kinetics experiment. Journal of Chemical Education. 62(10). 911–911. 6 indexed citations
15.
Minter, David E. & Manfred G. Reinecke. (1985). Two-cycle organic chemistry: An alternative to course proliferation. Journal of Chemical Education. 62(1). 77–77. 5 indexed citations
16.
Stotter, Philip L., et al.. (1985). Model studies of a conceptually new approach to the total synthesis of quinine. The Journal of Organic Chemistry. 50(1). 29–31. 14 indexed citations
17.
Blackburn, Brent, et al.. (1984). Substituent effects on the reductions of quinoline- -boranes. Tetrahedron Letters. 25(43). 4913–4916.
18.
Minter, David E. & Philip L. Stotter. (1982). ChemInform Abstract: EFFICIENT CONVERSIONS OF QUINOLINES TO N‐(CARBOALKOXY)‐1,2‐DIHYDROQUINOLINES. Chemischer Informationsdienst. 13(8). 1 indexed citations
19.
Minter, David E. & Philip L. Stotter. (1981). Efficient conversions of quinolines to N-(carboalkoxy)-1,2-dihydroquinolines. The Journal of Organic Chemistry. 46(20). 3965–3970. 16 indexed citations
20.
Minter, David E. & Gerhard J. Fonken. (1977). Cyclopropylallenes II. Thermolysis of 1-(cis-2-methylcyclopropyl)-1,2-bytadiene. Tetrahedron Letters. 18(48). 4149–4151. 3 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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