Steven J. Coote

1.5k total citations
31 papers, 1.1k citations indexed

About

Steven J. Coote is a scholar working on Organic Chemistry, Cancer Research and Molecular Biology. According to data from OpenAlex, Steven J. Coote has authored 31 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Organic Chemistry, 7 papers in Cancer Research and 5 papers in Molecular Biology. Recurrent topics in Steven J. Coote's work include Asymmetric Synthesis and Catalysis (20 papers), Synthetic Organic Chemistry Methods (12 papers) and Chemical synthesis and alkaloids (9 papers). Steven J. Coote is often cited by papers focused on Asymmetric Synthesis and Catalysis (20 papers), Synthetic Organic Chemistry Methods (12 papers) and Chemical synthesis and alkaloids (9 papers). Steven J. Coote collaborates with scholars based in United Kingdom, United States and Australia. Steven J. Coote's co-authors include Graham Dawson, Christopher G. Frost, Jonathan M. J. Williams, Stephen G. Davies, Joanne V. Allen, David Middlemiss, Alan Naylor, David M. Hodgson, Christopher J. Martin and Richard J. Whitby and has published in prestigious journals such as The Journal of Organic Chemistry, Tetrahedron and Organic Letters.

In The Last Decade

Steven J. Coote

31 papers receiving 1.1k citations

Peers

Steven J. Coote
Michael A. Calter United States
Antonio Saba Italy
Michele Gatti Switzerland
Leleti Rajender Reddy United States
Denis Lucet France
Damien Polet Switzerland
Xiyan Lu China
Roger Fässler Switzerland
Lydia McKinstry United States
Michelle R. Machacek United States
Michael A. Calter United States
Steven J. Coote
Citations per year, relative to Steven J. Coote Steven J. Coote (= 1×) peers Michael A. Calter

Countries citing papers authored by Steven J. Coote

Since Specialization
Citations

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

Fields of papers citing papers by Steven J. Coote

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Steven J. Coote

This figure shows the co-authorship network connecting the top 25 collaborators of Steven J. Coote. A scholar is included among the top collaborators of Steven J. Coote 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 Steven J. Coote. Steven J. Coote 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.
Coote, Steven J., Stephen G. Davies, Ai M. Fletcher, Paul M. Roberts, & James E. Thomson. (2010). Enantiospecific Stereodivergent Synthesis of trans‐ and cis‐N(2),3‐Dimethyl‐4‐phenyl‐1,2,3,4‐tetrahydroisoquinolines. Chemistry - An Asian Journal. 5(3). 589–604. 16 indexed citations
2.
Hodgson, David M., Christopher D. Bray, Nicholas D. Kindon, et al.. (2008). Synthesis andC-Alkylation of Hindered Aldehyde Enamines. The Journal of Organic Chemistry. 74(3). 1019–1028. 28 indexed citations
3.
Hodgson, David M., et al.. (2005). Deprotonation–electrophile trapping of terminal epoxides. Organic & Biomolecular Chemistry. 3(10). 1893–1893. 13 indexed citations
4.
Hodgson, David M., et al.. (2004). Substituted Epoxides by Lithiation of Terminal Epoxides. Organic Letters. 6(23). 4187–4189. 11 indexed citations
5.
6.
Whitby, Richard J., et al.. (2000). Early Transition Metal Induced Intramolecular Cocyclisation/Elaboration Reactions Using a Cleavable Silicon Linker. Synlett. 12(12). 1371–1374. 3 indexed citations
7.
Pass, Martin, Steven J. Coote, Harry Finch, et al.. (1999). Synthetic [5,5] trans-fused indane lactones as inhibitors of thrombin. Bioorganic & Medicinal Chemistry Letters. 9(3). 431–436. 9 indexed citations
8.
Coote, Steven J., et al.. (1996). 5-Bromobarbituric Acid : A Mild and Selective Monobrominating Agent Employed in the Synthesis of the Gastrin Antagonist GR174152. Synthetic Communications. 26(22). 4195–4209. 3 indexed citations
9.
Dawson, Graham, Jonathan M. J. Williams, & Steven J. Coote. (1995). Enantioselective synthesis of succinic acids and γ-lactones via palladium catalysed allylic substitution reactions. Tetrahedron Asymmetry. 6(10). 2535–2546. 60 indexed citations
10.
Allen, Joanne V., Steven J. Coote, Graham Dawson, et al.. (1995). ChemInform Abstract: Palladium‐Catalyzed Asymmetric Allylic Substitution: A Ligand Design Incorporating Steric and Electronic Effects.. ChemInform. 26(1). 1 indexed citations
11.
Allen, Joanne V., et al.. (1994). Palladium-catalysed asymmetric allylic substitution: a ligand design incorporating steric and electronic effects. Journal of the Chemical Society Perkin Transactions 1. 2065–2065. 121 indexed citations
12.
Dawson, Graham, Christopher G. Frost, Christopher J. Martin, Jonathan M. J. Williams, & Steven J. Coote. (1993). Sulfides tethered to oxazolines: Ligands for enantioselective catalysis. Tetrahedron Letters. 34(48). 7793–7796. 70 indexed citations
13.
Dawson, Graham, Christopher G. Frost, Jonathan M. J. Williams, & Steven J. Coote. (1993). Asymmetric palladium catalysed allylic substitution using phosphorus containing oxazoline ligands. Tetrahedron Letters. 34(19). 3149–3150. 393 indexed citations
14.
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Coote, Steven J., Stephen G. Davies, David Middlemiss, & Alan Naylor. (1989). Enantiospecific synthesis of (+)-(R)-6,7-dimethoxy-2-methyl-4-phenyl-1,2,3,4-tetrahydroisoquinoline from (+)-(S)-2-methylamino-1-phenylethanol (halostachine). Journal of the Chemical Society Perkin Transactions 1. 2223–2223. 19 indexed citations
16.
Coote, Steven J., Stephen G. Davies, David Middlemiss, & Alan Naylor. (1989). Stereoselective synthesis of cis-1,3-disubstituted 1,3-dihydroisobenzofurans via arenechromium tricarbonyl methodology. Journal of Organometallic Chemistry. 379(1-2). 81–88. 21 indexed citations
17.
Davies, Stephen G., George Bashiardes, R. Paul Beckett, et al.. (1988). Asymmetric synthesis via chiral transition metal auxiliaries. Philosophical Transactions of the Royal Society of London Series A Mathematical and Physical Sciences. 326(1592). 619–631. 5 indexed citations
18.
19.
Coote, Steven J., Stephen G. Davies, & Kevin H. Sutton. (1988). Tetrahydroisoquinolines. Part 4. Enantioselective conversion of (+)-amphetamine into (+)-(1R,3S,4S)- and (–)-(1S,3S,4R)-1,2,3,4-tetramethyl-1,2,3,4-tetrahydroisoquinoline via tricarbonyl(arene)chromium methodology. Journal of the Chemical Society Perkin Transactions 1. 1481–1487. 8 indexed citations
20.
Blagg, Julian, Steven J. Coote, Stephen G. Davies, David Middlemiss, & Alan Naylor. (1987). Tetrahydroisoquinolines. Part 3. Stereoselective synthesis of cis- and trans-1,4-disubstituted N-methyl-1,2,3,4-tetrahydroisoquinolines as their tricarbonylchromium complexes. Journal of the Chemical Society Perkin Transactions 1. 689–689. 17 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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