S.P. Stokes

974 total citations
27 papers, 501 citations indexed

About

S.P. Stokes is a scholar working on Organic Chemistry, Molecular Biology and Physical and Theoretical Chemistry. According to data from OpenAlex, S.P. Stokes has authored 27 papers receiving a total of 501 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Organic Chemistry, 11 papers in Molecular Biology and 5 papers in Physical and Theoretical Chemistry. Recurrent topics in S.P. Stokes's work include Crystallography and molecular interactions (5 papers), Crystallization and Solubility Studies (5 papers) and Catalytic C–H Functionalization Methods (4 papers). S.P. Stokes is often cited by papers focused on Crystallography and molecular interactions (5 papers), Crystallization and Solubility Studies (5 papers) and Catalytic C–H Functionalization Methods (4 papers). S.P. Stokes collaborates with scholars based in United Kingdom, Ireland and United States. S.P. Stokes's co-authors include Joseph P. A. Harrity, Simon E. Lawrence, Nigel S. Simpkins, Alan J. Whittle, Anita R. Maguire, K.S. Eccles, Richard I. Cooper, Nathaniel G. Martin, James S. Scott and H.A. Moynihan and has published in prestigious journals such as Cancer Research, Chemical Communications and Organic Letters.

In The Last Decade

S.P. Stokes

27 papers receiving 490 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
S.P. Stokes United Kingdom 13 275 144 139 132 45 27 501
Elena L. Luzina Russia 10 270 1.0× 72 0.5× 70 0.5× 82 0.6× 26 0.6× 18 413
K. Sunil India 12 173 0.6× 68 0.5× 97 0.7× 92 0.7× 29 0.6× 30 323
Eugene V. Babaev Russia 15 759 2.8× 147 1.0× 72 0.5× 92 0.7× 84 1.9× 146 913
Shunichirou Tsutsumi Japan 7 86 0.3× 122 0.8× 160 1.2× 174 1.3× 16 0.4× 8 352
Haresh Ajani Czechia 13 201 0.7× 155 1.1× 76 0.5× 60 0.5× 21 0.5× 19 413
Margaret A. McCarrick United States 11 389 1.4× 108 0.8× 73 0.5× 36 0.3× 23 0.5× 12 545
G. Rihs Switzerland 13 211 0.8× 128 0.9× 77 0.6× 127 1.0× 69 1.5× 23 546
Edyta Dyguda‐Kazimierowicz Poland 11 115 0.4× 168 1.2× 37 0.3× 63 0.5× 20 0.4× 22 354
Terukage Hirata Japan 8 211 0.8× 100 0.7× 130 0.9× 38 0.3× 64 1.4× 10 386
Lucia Lassiani Italy 11 154 0.6× 139 1.0× 71 0.5× 39 0.3× 17 0.4× 42 339

Countries citing papers authored by S.P. Stokes

Since Specialization
Citations

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

Fields of papers citing papers by S.P. Stokes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by S.P. Stokes. 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 S.P. Stokes. The network helps show where S.P. Stokes may publish in the future.

Co-authorship network of co-authors of S.P. Stokes

This figure shows the co-authorship network connecting the top 25 collaborators of S.P. Stokes. A scholar is included among the top collaborators of S.P. Stokes 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 S.P. Stokes. S.P. Stokes 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.
Lorthioir, Olivier, et al.. (2021). Transfer of photochemistry from UV to visible: An expedient access to a bridged pyrrolidine. Tetrahedron Letters. 84. 153447–153447. 5 indexed citations
2.
Degorce, Sébastien L., Rana Anjum, Keith Dillman, et al.. (2018). Optimization of permeability in a series of pyrrolotriazine inhibitors of IRAK4. Bioorganic & Medicinal Chemistry. 26(4). 913–924. 15 indexed citations
3.
Stokes, S.P., et al.. (2017). Will they co-crystallize?. CrystEngComm. 19(36). 5336–5340. 82 indexed citations
4.
Stokes, S.P., et al.. (2017). Pd-Catalyzed C–H aziridination of 3,3,5,5-tetrasubstituted piperazin-2-ones. Organic & Biomolecular Chemistry. 16(1). 53–56. 3 indexed citations
5.
Stokes, S.P., et al.. (2016). Synthesis of Electron-Deficient N1-(Hetero)aryl 3,3,5,5-Tetramethyl Piperazinones. Synlett. 28(3). 357–361. 1 indexed citations
6.
Stokes, S.P., et al.. (2016). Practical synthesis of 3,3-substituted dihydroquinoxalin-2-ones from aryl 1,2-diamines using the Bargellini reaction. Tetrahedron Letters. 57(39). 4386–4388. 9 indexed citations
7.
Massey, Andrew J., S.P. Stokes, Helen Browne, et al.. (2015). Identification of novel,in vivoactive Chk1 inhibitors utilizing structure guided drug design. Oncotarget. 6(34). 35797–35812. 34 indexed citations
8.
Simpson, Iain, Stephen A. St-Gallay, S.P. Stokes, David Whittaker, & Rafal Wiewiora. (2015). An efficient one-pot synthesis of 2-bromo-6-aryl[5H]pyrrolo[2,3-b]pyrazines. Tetrahedron Letters. 56(12). 1492–1495. 5 indexed citations
9.
Stokes, S.P., Colin C. Seaton, K.S. Eccles, Anita R. Maguire, & Simon E. Lawrence. (2014). Insight into the Mechanism of Formation of Channel Hydrates via Templating. Crystal Growth & Design. 14(3). 1158–1166. 13 indexed citations
10.
Webber, Matthew J., D.M. Grainger, Matthew Weston, et al.. (2013). Towards the enantioselective synthesis of (−)-euonyminol – preparation of a fully functionalised lower-rim model. Organic & Biomolecular Chemistry. 11(15). 2514–2514. 17 indexed citations
11.
Stokes, S.P., et al.. (2012). Synthesis of anti and syn hydroxy-iso-evoninic acids. Organic & Biomolecular Chemistry. 10(24). 4685–4685. 4 indexed citations
12.
Eccles, K.S., S.P. Stokes, Noel M. O’Boyle, et al.. (2012). Utilizing Sulfoxide···Iodine Halogen Bonding for Cocrystallization. Crystal Growth & Design. 12(6). 2969–2977. 26 indexed citations
13.
Stokes, S.P. & Nathaniel G. Martin. (2012). A simple and efficient synthesis of N-benzoyl ureas. Tetrahedron Letters. 53(36). 4802–4804. 13 indexed citations
14.
Eccles, K.S., S.P. Stokes, W.B. Jennings, et al.. (2010). Evaluation of the Bruker SMART X2S: crystallography for the nonspecialist?. Journal of Applied Crystallography. 44(1). 213–215. 33 indexed citations
15.
Eccles, K.S., et al.. (2010). Sulfoxides: Potent Co-Crystal Formers. Crystal Growth & Design. 10(10). 4243–4245. 26 indexed citations
16.
Scheinmann, Feodor, Jonathan F. Hull, S.P. Stokes, & Andrew V. Stachulski. (1998). ChemInform Abstract: New Synthesis of Chiral Compounds. ChemInform. 29(15). 2 indexed citations
17.
18.
Cohen, Theodore & S.P. Stokes. (1993). The mechanisms of n-butyllithium induced β-cleavage of 2-methyltetrahydrofuran and oxepane. Tetrahedron Letters. 34(50). 8023–8024. 3 indexed citations
19.
Simpkins, Nigel S., S.P. Stokes, & Alan J. Whittle. (1992). An enantiospecific total synthesis of allosamizoline. Tetrahedron Letters. 33(6). 793–796. 21 indexed citations
20.
Simpkins, Nigel S., S.P. Stokes, & Alan J. Whittle. (1992). An enantiospecific synthesis of allosamizoline. Journal of the Chemical Society Perkin Transactions 1. 2471–2471. 23 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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