Thomas E. Storr

807 total citations
21 papers, 672 citations indexed

About

Thomas E. Storr is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, Thomas E. Storr has authored 21 papers receiving a total of 672 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Organic Chemistry, 6 papers in Molecular Biology and 3 papers in Inorganic Chemistry. Recurrent topics in Thomas E. Storr's work include Catalytic C–H Functionalization Methods (12 papers), Catalytic Cross-Coupling Reactions (9 papers) and Synthesis and Catalytic Reactions (4 papers). Thomas E. Storr is often cited by papers focused on Catalytic C–H Functionalization Methods (12 papers), Catalytic Cross-Coupling Reactions (9 papers) and Synthesis and Catalytic Reactions (4 papers). Thomas E. Storr collaborates with scholars based in United Kingdom, United States and China. Thomas E. Storr's co-authors include Ian J. S. Fairlamb, Christoph G. Baumann, Michael F. Greaney, Robert A. Stockman, Sara De Ornellas, Thomas J. Williams, Steven M. Howdle, Adrian C. Whitwood, R.J. Thatcher and Bert U. W. Maes and has published in prestigious journals such as Angewandte Chemie International Edition, Chemical Communications and The Journal of Organic Chemistry.

In The Last Decade

Thomas E. Storr

20 papers receiving 660 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas E. Storr United Kingdom 14 601 115 61 54 45 21 672
I. Held Germany 7 312 0.5× 145 1.3× 138 2.3× 18 0.3× 39 0.9× 7 412
Matteo Lanzi Italy 14 452 0.8× 94 0.8× 29 0.5× 13 0.2× 30 0.7× 29 518
Amer El‐Batta United States 7 286 0.5× 37 0.3× 71 1.2× 26 0.5× 33 0.7× 10 361
John Kallikat Augustine India 13 585 1.0× 81 0.7× 179 2.9× 12 0.2× 17 0.4× 26 679
B. Schetter Germany 9 515 0.9× 156 1.4× 151 2.5× 12 0.2× 11 0.2× 12 612
Gagan Chouhan India 13 606 1.0× 73 0.6× 171 2.8× 16 0.3× 15 0.3× 14 712
Elliad R. Silcoff Israel 6 383 0.6× 163 1.4× 109 1.8× 11 0.2× 17 0.4× 7 442
Brahmam Pujala India 6 277 0.5× 66 0.6× 115 1.9× 10 0.2× 31 0.7× 10 361
Derek M. Dalton United States 11 639 1.1× 188 1.6× 46 0.8× 20 0.4× 65 1.4× 17 693
Chintam Narayana India 13 334 0.6× 92 0.8× 149 2.4× 47 0.9× 9 0.2× 19 429

Countries citing papers authored by Thomas E. Storr

Since Specialization
Citations

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

Fields of papers citing papers by Thomas E. Storr

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Thomas E. Storr. 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 Thomas E. Storr. The network helps show where Thomas E. Storr may publish in the future.

Co-authorship network of co-authors of Thomas E. Storr

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas E. Storr. A scholar is included among the top collaborators of Thomas E. Storr 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 Thomas E. Storr. Thomas E. Storr 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.
Monaco, Serena, G. R. Stephenson, Thomas E. Storr, et al.. (2025). 3,3′-Diindolylmethane (DIM): A Molecular Scaffold for Inhibition of WWP1 and WWP2, Members of the NEDD4 Family HECT E3 Ligases. ACS Omega. 10(6). 5963–5972. 2 indexed citations
2.
Stephenson, G. R., et al.. (2024). Expanding the inhibitor space of the WWP1 and WWP2 HECT E3 ligases. Journal of Enzyme Inhibition and Medicinal Chemistry. 39(1). 2394895–2394895. 1 indexed citations
3.
Fotso, Ghislain W., Bathélémy Ngameni, Thomas E. Storr, et al.. (2020). Synthesis of Novel Stilbene–Coumarin Derivatives and Antifungal Screening of Monotes kerstingii-Specialized Metabolites Against Fusarium oxysporum. Antibiotics. 9(9). 537–537. 5 indexed citations
4.
Chidipudi, Suresh Reddy, William Lewis, Daniel Hamza, et al.. (2018). PdII‐Mediated Oxidative Amination for Access to a 9‐Azabicyclo[4.2.1]nonane Compound Library and Anatoxin‐a. European Journal of Organic Chemistry. 2018(40). 5558–5561. 3 indexed citations
5.
Šiaučiulis, Mindaugas, et al.. (2016). Versatile C(sp2)−C(sp3) Ligand Couplings of Sulfoxides for the Enantioselective Synthesis of Diarylalkanes. Angewandte Chemie International Edition. 55(34). 10013–10016. 34 indexed citations
6.
Šiaučiulis, Mindaugas, et al.. (2016). Versatile C(sp2)−C(sp3) Ligand Couplings of Sulfoxides for the Enantioselective Synthesis of Diarylalkanes. Angewandte Chemie. 128(34). 10167–10170. 6 indexed citations
7.
Storr, Thomas E., Michael J. Rawling, Daniel Hamza, et al.. (2016). Expedient synthesis of an atypical oxazolidinone compound library. Bioorganic & Medicinal Chemistry. 24(21). 5249–5257. 5 indexed citations
8.
Storr, Thomas E., Christopher J. Teskey, & Michael F. Greaney. (2016). Cross‐Dehydrogenative‐Coupling of Alkoxybenzenes with Toluenes: Copper(II) Halide Mediated Tandem Halo/Benzylation of Arenes. Chemistry - A European Journal. 22(50). 18169–18178. 11 indexed citations
9.
Storr, Thomas E., et al.. (2016). Progress in the synthesis of sustainable polymers from terpenes and terpenoids. Green Materials. 4(3). 115–134. 92 indexed citations
10.
Rawling, Michael J., Thomas E. Storr, Wafa A. Bawazir, et al.. (2015). Facile access to a heterocyclic, sp3-rich chemical scaffold via a tandem condensation/intramolecular nitrone–alkene [3+2] cycloaddition strategy. Chemical Communications. 51(64). 12867–12870. 20 indexed citations
11.
Storr, Thomas E., Michael J. Rawling, William Lewis, et al.. (2014). Combining two-directional synthesis and tandem reactions. Part 21: Exploitation of a dimeric macrocycle for chain terminus differentiation and synthesis of an sp3-rich library. Bioorganic & Medicinal Chemistry. 23(11). 2621–2628. 15 indexed citations
12.
Storr, Thomas E., et al.. (2014). Palladium catalysed cross-dehydrogenative-coupling of 1,3,5-trialkoxybenzenes with simple arenes. Chemical Communications. 50(87). 13275–13277. 15 indexed citations
14.
Peschiulli, Aldo, Thomas E. Storr, Emily A. Mitchell, et al.. (2013). Ruthenium‐Catalyzed α‐(Hetero)Arylation of Saturated Cyclic Amines: Reaction Scope and Mechanism. Chemistry - A European Journal. 19(31). 10378–10387. 48 indexed citations
15.
Storr, Thomas E. & Michael F. Greaney. (2013). Palladium-Catalyzed Arylation of Simple Arenes with Iodonium Salts. Organic Letters. 15(6). 1410–1413. 57 indexed citations
16.
Bergman, Sheba D., et al.. (2012). The Role of the Alcohol and Carboxylic Acid in Directed Ruthenium‐Catalyzed C(sp3)H α‐Alkylation of Cyclic Amines. Chemistry - A European Journal. 18(33). 10393–10398. 55 indexed citations
17.
Ornellas, Sara De, Thomas E. Storr, Thomas J. Williams, Christoph G. Baumann, & Ian J. S. Fairlamb. (2011). Direct C-H/C-X Coupling Methodologies Mediated by Pd/Cu or Cu: An Examination of the Synthetic Applications and Mechanistic Findings. Current Organic Synthesis. 8(1). 79–101. 29 indexed citations
18.
19.
Storr, Thomas E., Christoph G. Baumann, R.J. Thatcher, et al.. (2009). Pd(0)/Cu(I)-Mediated Direct Arylation of 2′-Deoxyadenosines: Mechanistic Role of Cu(I) and Reactivity Comparisons with Related Purine Nucleosides. The Journal of Organic Chemistry. 74(16). 5810–5821. 76 indexed citations
20.

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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