David T. MacPherson

913 total citations
24 papers, 533 citations indexed

About

David T. MacPherson is a scholar working on Organic Chemistry, Molecular Biology and Cancer Research. According to data from OpenAlex, David T. MacPherson has authored 24 papers receiving a total of 533 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Organic Chemistry, 9 papers in Molecular Biology and 4 papers in Cancer Research. Recurrent topics in David T. MacPherson's work include Chemical Synthesis and Analysis (4 papers), Synthesis and Biological Activity (4 papers) and Synthetic Organic Chemistry Methods (4 papers). David T. MacPherson is often cited by papers focused on Chemical Synthesis and Analysis (4 papers), Synthesis and Biological Activity (4 papers) and Synthetic Organic Chemistry Methods (4 papers). David T. MacPherson collaborates with scholars based in United Kingdom, United States and Sweden. David T. MacPherson's co-authors include Barry M. Trost, Chuen Chan, Mark Lautens, Gerald J. Tanoury, Visuvanathar Sridharan, Ronald Grigg, William S. MacLachlan, Alan T. Hewson, Mark Thornton‐Pett and H. Ali Döndaş and has published in prestigious journals such as Journal of the American Chemical Society, Chemical Communications and The Journal of Organic Chemistry.

In The Last Decade

David T. MacPherson

23 papers receiving 512 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 T. MacPherson United Kingdom 11 418 104 44 40 33 24 533
Pelin Kelicen Türkiye 11 711 1.7× 131 1.3× 5 0.1× 24 0.6× 61 1.8× 22 875
Nitesh Kumar Nandwana India 16 551 1.3× 185 1.8× 6 0.1× 55 1.4× 16 0.5× 29 702
Linda E. Keown United States 9 329 0.8× 149 1.4× 5 0.1× 12 0.3× 71 2.2× 11 577
Bengt Ek Sweden 10 133 0.3× 126 1.2× 26 0.6× 17 0.4× 26 0.8× 13 361
Michael P. DeMartino United States 7 506 1.2× 74 0.7× 13 0.3× 54 1.4× 27 0.8× 12 581
Andrew J. Culshaw United Kingdom 8 453 1.1× 53 0.5× 5 0.1× 30 0.8× 65 2.0× 13 521
Gao‐Feng Shi China 10 157 0.4× 109 1.0× 36 0.8× 3 0.1× 20 0.6× 16 340
R. R. Crenshaw United States 10 220 0.5× 74 0.7× 8 0.2× 17 0.4× 34 1.0× 25 345
Young‐Shin Kwak South Korea 12 269 0.6× 182 1.8× 3 0.1× 44 1.1× 45 1.4× 26 485
Andrés S. Hernández United States 9 182 0.4× 128 1.2× 16 0.4× 6 0.1× 8 0.2× 17 285

Countries citing papers authored by David T. MacPherson

Since Specialization
Citations

This map shows the geographic impact of David T. MacPherson'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 T. MacPherson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David T. MacPherson more than expected).

Fields of papers citing papers by David T. MacPherson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David T. MacPherson

This figure shows the co-authorship network connecting the top 25 collaborators of David T. MacPherson. A scholar is included among the top collaborators of David T. MacPherson 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 T. MacPherson. David T. MacPherson 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.
Witty, David R., Giuseppe Alvaro, Gerard M.P. Giblin, et al.. (2020). Discovery of Vixotrigine: A Novel Use-Dependent Sodium Channel Blocker for the Treatment of Trigeminal Neuralgia. ACS Medicinal Chemistry Letters. 11(9). 1678–1687. 17 indexed citations
2.
Churcher, Ian, et al.. (2011). On the utility of S-mesitylsulfinimines for the stereoselective synthesis of chiral amines and aziridines. Chemical Communications. 47(26). 7491–7491. 20 indexed citations
3.
Sanger, Gareth J., Susan M. Westaway, Ashley Barnes, et al.. (2009). GSK962040: a small molecule, selective motilin receptor agonist, effective as a stimulant of human and rabbit gastrointestinal motility. Neurogastroenterology & Motility. 21(6). 657–657. 65 indexed citations
4.
MacPherson, David T., et al.. (2007). Convenient synthesis of chiral non-racemic S-mesityl sulfinimines. Tetrahedron Letters. 49(7). 1129–1132. 8 indexed citations
5.
6.
Grigg, Ronald, William S. MacLachlan, David T. MacPherson, et al.. (2000). Pictet–Spengler/Palladium Catalyzed Allenylation and Carbonylation Processes. Tetrahedron. 56(35). 6585–6594. 48 indexed citations
7.
Döndaş, H. Ali, Ronald Grigg, William S. MacLachlan, et al.. (2000). Sequential 1,3-Dipolar Cycloaddition-Pictet–Spengler Reactions. A Versatile Tactical Combination. Tetrahedron. 56(24). 4063–4070. 21 indexed citations
8.
Döndaş, H. Ali, Ronald Grigg, William S. MacLachlan, et al.. (2000). Solid phase sequential 1,3-dipolar cycloaddition–Pictet–Spengler reactions. Tetrahedron Letters. 41(6). 967–970. 37 indexed citations
9.
Bailey, Stuart, Brian Bolognese, Andrew Faller, et al.. (1999). Selective inhibition of low affinity IgE receptor (CD23) processing: P1′ bicyclomethyl substituents. Bioorganic & Medicinal Chemistry Letters. 9(21). 3165–3170. 5 indexed citations
10.
Corbett, David F., et al.. (1995). Synthesis and Antifungal Activity of C-16 Oximino and Vinyl Amphotericin B Derivatives.. The Journal of Antibiotics. 48(6). 509–515. 2 indexed citations
11.
Trost, Barry M., Gerald J. Tanoury, Mark Lautens, Carmel T. Chan, & David T. MacPherson. (1994). ChemInform Abstract: Pd‐Catalyzed Cycloisomerization to 1,2‐Dialkylidenecycloalkanes. Part 1.. ChemInform. 25(40). 1 indexed citations
12.
Taylor, Andrew W. & David T. MacPherson. (1994). Preparation of a Novel C-13 Thioacetal Derivative of Amphotericin B. Tetrahedron Letters. 35(29). 5289–5292. 5 indexed citations
13.
MacPherson, David T., et al.. (1993). ChemInform Abstract: Adventures in Polyene Macrolide Chemistry: The Derivatization of Amphotericin B. ChemInform. 24(43). 3 indexed citations
14.
Driver, Michael J., et al.. (1992). Synthesis of 16-decarboxy-16-hydroxymethyl amphotericin B - a novel antifungal agent. Tetrahedron Letters. 33(30). 4357–4360. 7 indexed citations
15.
Driver, Michael J., William S. MacLachlan, David T. MacPherson, & Simon A. Readshaw. (1990). The chemistry of amphotericin B. Synthesis of 13,14-anhydro derivatives. Journal of the Chemical Society Chemical Communications. 636–636. 3 indexed citations
16.
Trost, Barry M. & David T. MacPherson. (1987). [4 + 3] Cycloaddition of a trimethylenemethane fragment. An approach to polyhydroazulenes. Journal of the American Chemical Society. 109(11). 3483–3484. 69 indexed citations
17.
Hewson, Alan T. & David T. MacPherson. (1985). Total synthesis of cyclopentanoid natural products. Journal of the Chemical Society Perkin Transactions 1. 2625–2625. 17 indexed citations
18.
Hewson, Alan T. & David T. MacPherson. (1984). ChemInform Abstract: SYNTHESIS OF A HIGHLY FUNCTIONALIZED BICYCLO(3.3.0)OCTANE. Chemischer Informationsdienst. 15(16).
19.
Hewson, Alan T. & David T. MacPherson. (1983). Synthesis of a highly functionalised bicyclo[3.3.0]octane. Tetrahedron Letters. 24(51). 5807–5808. 9 indexed citations
20.
Hewson, Alan T. & David T. MacPherson. (1983). Conjugate addition to the ethylene ketal of 2-carbomethoxy-2-cyclopentenone a synthesis of sarkomycin. Tetrahedron Letters. 24(6). 647–648. 11 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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