Richard Luke

1.2k total citations
23 papers, 471 citations indexed

About

Richard Luke is a scholar working on Molecular Biology, Organic Chemistry and Cancer Research. According to data from OpenAlex, Richard Luke has authored 23 papers receiving a total of 471 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 14 papers in Organic Chemistry and 4 papers in Cancer Research. Recurrent topics in Richard Luke's work include Chemical Synthesis and Analysis (8 papers), Synthetic Organic Chemistry Methods (5 papers) and Chemical Synthesis and Reactions (5 papers). Richard Luke is often cited by papers focused on Chemical Synthesis and Analysis (8 papers), Synthetic Organic Chemistry Methods (5 papers) and Chemical Synthesis and Reactions (5 papers). Richard Luke collaborates with scholars based in United Kingdom and United States. Richard Luke's co-authors include Gordon S. Currie, Laurence M. Harwood, Michael G. B. Drew, Mark Bradley, Barry R. Hayter, John D. Sutherland, Andrew N. Boa, Simon T. Barry, A. Peter Johnson and David A. Pears and has published in prestigious journals such as The EMBO Journal, Chemical Communications and Journal of Medicinal Chemistry.

In The Last Decade

Richard Luke

23 papers receiving 454 citations

Peers

Richard Luke
Robert J. Halter United States
Fernando Ferrer United States
Luca Mannocci Switzerland
Richard M. Deans United States
Ronghui Lin United States
Michael Friedmann United States
Tae Kyo Park United States
Robert J. Halter United States
Richard Luke
Citations per year, relative to Richard Luke Richard Luke (= 1×) peers Robert J. Halter

Countries citing papers authored by Richard Luke

Since Specialization
Citations

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

Fields of papers citing papers by Richard Luke

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Richard Luke. 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 Richard Luke. The network helps show where Richard Luke may publish in the future.

Co-authorship network of co-authors of Richard Luke

This figure shows the co-authorship network connecting the top 25 collaborators of Richard Luke. A scholar is included among the top collaborators of Richard Luke 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 Richard Luke. Richard Luke 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
2.
Luke, Richard, Peter Ballard, David Buttar, et al.. (2009). Novel thienopyrimidine and thiazolopyrimidine kinase inhibitors with activity against Tie-2 in vitro and in vivo. Bioorganic & Medicinal Chemistry Letters. 19(23). 6670–6674. 31 indexed citations
3.
Luke, Richard, Ed Griffen, Neil J. Hales, et al.. (2009). In vitro pharmacological profiles of kinase inhibitors: Comparison with other pharmaceuticals. Journal of Pharmacological and Toxicological Methods. 60(2). 219–219. 1 indexed citations
4.
Davies, Barry R., Philippa Dudley, Sabina Cosulich, et al.. (2009). Abstract C208: CCT129254 (AT11854) is a well tolerated, orally bioavailable inhibitor of AKT/PKB with pharmacodynamic and antitumor activity in a range of xenograft models. Molecular Cancer Therapeutics. 8(12_Supplement). C208–C208. 3 indexed citations
5.
Buttar, David, Martina Fitzek, Barry R. Hayter, et al.. (2008). Discovery of imidazole vinyl pyrimidines as a novel class of kinase inhibitors which inhibit Tie-2 and are orally bioavailable. Bioorganic & Medicinal Chemistry Letters. 18(16). 4723–4726. 6 indexed citations
6.
Norman, Richard A., Simon T. Barry, J. Breed, et al.. (2004). Crystal Structure of Human Thymidine Phosphorylase in Complex with a Small Molecule Inhibitor. Structure. 12(1). 75–84. 86 indexed citations
7.
Reigan, Philip, Philip N. Edwards, Abdul M Gbaj, et al.. (2004). Aminoimidazolylmethyluracil Analogues as Potent Inhibitors of Thymidine Phosphorylase and Their Bioreductive Nitroimidazolyl Prodrugs. Journal of Medicinal Chemistry. 48(2). 392–402. 43 indexed citations
8.
Luke, Richard, et al.. (2003). Synthesis of Cytidine Ribonucleotides by Stepwise Assembly of the Heterocycle on a Sugar Phosphate. ChemBioChem. 4(6). 504–507. 42 indexed citations
9.
Pears, David A., et al.. (2003). Improving resins for solid phase synthesis: incorporation of 1-[2-(2-methoxyethoxy)ethoxy]-4-vinyl-benzene. Tetrahedron. 59(36). 7163–7169. 11 indexed citations
10.
Pears, David A., et al.. (2001). Ketoester methacrylate resin, secondary amine clean-up in the presence of primary amines. Journal of the Chemical Society Perkin Transactions 1. 1947–1952. 8 indexed citations
11.
Pears, David A., et al.. (2001). Synthesis of Resins via Multiparallel Suspension Polymerization. Journal of Combinatorial Chemistry. 3(6). 631–633. 16 indexed citations
12.
Currie, Gordon S., Michael G. B. Drew, Laurence M. Harwood, et al.. (2000). Chirally templated boronic acid Mannich reaction in the synthesis of optically active α-amino acids. Journal of the Chemical Society Perkin Transactions 1. 2982–2990. 31 indexed citations
13.
Luke, Richard, et al.. (2000). Thermally cleavable safety-catch linkers for solid phase chemistry. Tetrahedron Letters. 41(27). 5287–5290. 13 indexed citations
14.
Pears, David A., et al.. (2000). Acetoacetoxy ethyl methacrylate (AAEM) resin, a new scavenger for primary amines in the presence of secondary amines. Tetrahedron Letters. 41(46). 8963–8967. 15 indexed citations
15.
Johnson, Adam, Richard Luke, & Andrew N. Boa. (1996). Reactions of 1-acylamino-1-(trimethylsiloxy)alkanes: versatile precursors to acylimines. Journal of the Chemical Society Perkin Transactions 1. 895–895. 13 indexed citations
16.
Breeze, Alexander L., et al.. (1996). Structure of a specific peptide complex of the carboxy-terminal SH2 domain from the p85 alpha subunit of phosphatidylinositol 3-kinase.. The EMBO Journal. 15(14). 3579–3589. 48 indexed citations
17.
Luke, Richard, et al.. (1996). ‘One-pot’ methylation of Fmoc amino acids. Tetrahedron Letters. 37(2). 263–266. 13 indexed citations
18.
Gordon, Robert D., et al.. (1995). Purification and characterization of endogenous peptides extracted from HLA‐DR isolated from the spleen of a patient with rheumatoid arthritis. European Journal of Immunology. 25(5). 1473–1476. 14 indexed citations
19.
Bradbury, Robert H., Michael Robert Dennis, Eric F. Fisher, et al.. (1993). Quinoline, 1,5-naphthyridine and pyridine derivatives as potent, nonpeptidic angiotensin II receptor antagonists. Bioorganic & Medicinal Chemistry Letters. 3(5). 899–904. 8 indexed citations
20.
Johnson, A. Peter, et al.. (1986). Condensation of N,N-bis(trimethylsilyl)formamide with aldehydes: a general method for the synthesis of 1-formamido-1-trimethylsilyloxyalkanes. Journal of the Chemical Society Chemical Communications. 1658–1658. 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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