David J. Rawson

720 total citations
18 papers, 440 citations indexed

About

David J. Rawson is a scholar working on Organic Chemistry, Molecular Biology and Physiology. According to data from OpenAlex, David J. Rawson has authored 18 papers receiving a total of 440 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Organic Chemistry, 9 papers in Molecular Biology and 5 papers in Physiology. Recurrent topics in David J. Rawson's work include Asymmetric Synthesis and Catalysis (5 papers), Pain Mechanisms and Treatments (4 papers) and Chemical Synthesis and Analysis (3 papers). David J. Rawson is often cited by papers focused on Asymmetric Synthesis and Catalysis (5 papers), Pain Mechanisms and Treatments (4 papers) and Chemical Synthesis and Analysis (3 papers). David J. Rawson collaborates with scholars based in United Kingdom, United States and Japan. David J. Rawson's co-authors include A. I. MEYERS, Anton Meier, Ian Paterson, Jonathan M. J. Williams, Christopher J. Martin, Henk E. Moorlag, Todd D. Nelson, Kevin N. Dack, Roger P. Dickinson and Kim James and has published in prestigious journals such as Journal of Medicinal Chemistry, The Journal of Organic Chemistry and Tetrahedron.

In The Last Decade

David J. Rawson

18 papers receiving 425 citations

Peers

David J. Rawson
Piyasena Hewawasam United States
John M. Janusz United States
Ana Minatti United States
Daniel B. Horne United States
Graham N. Maw United Kingdom
Kathleen S. Zandi United States
Mark A. Hilfiker United States
Steven M. Sparks United States
Paul C. Fritch United States
Piyasena Hewawasam United States
David J. Rawson
Citations per year, relative to David J. Rawson David J. Rawson (= 1×) peers Piyasena Hewawasam

Countries citing papers authored by David J. Rawson

Since Specialization
Citations

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

Fields of papers citing papers by David J. Rawson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David J. Rawson

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

All Works

18 of 18 papers shown
1.
Bagal, Sharan K., Peter J. Bungay, Karl R. Gibson, et al.. (2015). Discovery and Optimization of Selective Na v 1.8 Modulator Series That Demonstrate Efficacy in Preclinical Models of Pain. ACS Medicinal Chemistry Letters. 6(6). 650–654. 36 indexed citations
2.
Rawson, David J., Delphine Brugier, Anthony Harrison, et al.. (2011). Part 3: Design and synthesis of proline-derived α2δ ligands. Bioorganic & Medicinal Chemistry Letters. 21(12). 3771–3773. 6 indexed citations
3.
Ryckmans, Thomas, Aisah A. Aubdool, Jennifer V. Bodkin, et al.. (2011). Design and pharmacological evaluation of PF-4840154, a non-electrophilic reference agonist of the TrpA1 channel. Bioorganic & Medicinal Chemistry Letters. 21(16). 4857–4859. 35 indexed citations
4.
Rawson, David J., Delphine Brugier, Anthony Harrison, et al.. (2011). Part 2: Design, synthesis and evaluation of hydroxyproline-derived α2δ ligands. Bioorganic & Medicinal Chemistry Letters. 21(12). 3767–3770. 3 indexed citations
5.
Rawson, David J., et al.. (2010). Isoform-Selective Voltage-Gated Na + Channel Modulators as Next-Generation Analgesics. Future Medicinal Chemistry. 2(5). 775–790. 14 indexed citations
6.
Allerton, Charlotte, Chris Barber, Kevin Beaumont, et al.. (2006). A Novel Series of Potent and Selective PDE5 Inhibitors with Potential for High and Dose-Independent Oral Bioavailability. Journal of Medicinal Chemistry. 49(12). 3581–3594. 18 indexed citations
7.
MEYERS, A. I., Todd D. Nelson, Henk E. Moorlag, David J. Rawson, & Anton Meier. (2004). Chiral oxazoline route to enantiomerically pure biphenyls: magnesio and copper mediated asymmetric hetero- and homo-coupling reactions. Tetrahedron. 60(20). 4459–4473. 63 indexed citations
8.
Rawson, David J., Kevin N. Dack, Roger P. Dickinson, et al.. (2004). The Design and Synthesis of a Novel, Orally Active, Selective ETA Antagonist. Medicinal Chemistry Research. 13(3-4). 149–157. 3 indexed citations
9.
Rawson, David J., Kevin N. Dack, Roger P. Dickinson, & Kim James. (2002). The design and synthesis of a novel series of indole derived selective ETA antagonists. Bioorganic & Medicinal Chemistry Letters. 12(2). 125–128. 33 indexed citations
10.
Walker, Donald K., Kevin N. Dack, Roger P. Dickinson, et al.. (2001). Absorption, distribution, metabolism, and excretion considerations in selection of orally active indole-containing endothelin antagonist.. PubMed. 29(11). 1424–31. 6 indexed citations
11.
Martin, Christopher J., David J. Rawson, & Jonathan M. J. Williams. (1998). The preparation of enantiomerically enriched γ-amino acids (GABAs) using palladium catalysed allylic substitution. Tetrahedron Asymmetry. 9(20). 3723–3730. 31 indexed citations
12.
Bower, Justin, Christopher J. Martin, David J. Rawson, Alexandra M. Z. Slawin, & Jonathan M. J. Williams. (1996). Diastereoselective conversion of sulfides into sulfoxides. 1,5- and 1,6-asymmetric induction. Journal of the Chemical Society Perkin Transactions 1. 333–333. 21 indexed citations
13.
Rawson, David J. & A. I. MEYERS. (1992). The asymmetric reduction of prochiral ketones using (S)-2,2′-dihydroxy-4,5,6,4′,5′,6′-hexamethoxybiphenyl. Journal of the Chemical Society Chemical Communications. 494–496. 21 indexed citations
14.
MEYERS, A. I., Anton Meier, & David J. Rawson. (1992). A highly stereoselective synthesis of axially chiral biaryls. Application to the synthesis of a potential chiral catalysts.. Tetrahedron Letters. 33(7). 853–856. 46 indexed citations
15.
Rawson, David J. & A. I. MEYERS. (1991). Asymmetric tandem additions to chiral naphthyloxazolines. A new and potent chiral auxiliary resulting in a major improvement in convenience and efficiency. The Journal of Organic Chemistry. 56(7). 2292–2294. 40 indexed citations
16.
Rawson, David J. & A. I. MEYERS. (1991). Highly reactive organolithiums (from “Freeman's Reagent”) and their additions to naphthalene oxazolines.. Tetrahedron Letters. 32(19). 2095–2098. 19 indexed citations
17.
Paterson, Ian & David J. Rawson. (1989). Studies in macrolide synthesis: A highly stereoselective synthesis of (+)-(9S)-dihydroerythronolide a using macrocyclic stereocontrol. Tetrahedron Letters. 30(52). 7463–7466. 30 indexed citations
18.
Paterson, Ian, et al.. (1988). Studies in macrolide synthesis: A concise asymmetric synthesis of a macrolide intermediate for the erythronolides.. Tetrahedron Letters. 29(12). 1461–1464. 15 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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