Thomas C. Stephens

579 total citations
10 papers, 494 citations indexed

About

Thomas C. Stephens is a scholar working on Organic Chemistry, Molecular Biology and Spectroscopy. According to data from OpenAlex, Thomas C. Stephens has authored 10 papers receiving a total of 494 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Organic Chemistry, 5 papers in Molecular Biology and 2 papers in Spectroscopy. Recurrent topics in Thomas C. Stephens's work include Chemical Synthesis and Analysis (5 papers), Catalytic C–H Functionalization Methods (3 papers) and Synthetic Organic Chemistry Methods (3 papers). Thomas C. Stephens is often cited by papers focused on Chemical Synthesis and Analysis (5 papers), Catalytic C–H Functionalization Methods (3 papers) and Synthetic Organic Chemistry Methods (3 papers). Thomas C. Stephens collaborates with scholars based in United Kingdom and France. Thomas C. Stephens's co-authors include William P. Unsworth, Graham Pattison, Ryan G. Epton, Jason M. Lynam, Thomas French, James A. Rossi‐Ashton, Lodi Mahendar, Hon Eong Ho, Richard J. K. Taylor and Peter O’Brien and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and ACS Catalysis.

In The Last Decade

Thomas C. Stephens

10 papers receiving 488 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 C. Stephens United Kingdom 10 478 176 48 34 32 10 494
Ji Hyeon Gong South Korea 7 369 0.8× 130 0.7× 46 1.0× 26 0.8× 14 0.4× 7 378
Andriy V. Tymtsunik Ukraine 12 360 0.8× 92 0.5× 68 1.4× 16 0.5× 74 2.3× 26 397
Sheng‐Ying Hsieh Switzerland 9 438 0.9× 132 0.8× 114 2.4× 36 1.1× 23 0.7× 11 477
Marta G. Núñez Spain 5 389 0.8× 113 0.6× 124 2.6× 21 0.6× 35 1.1× 8 411
H. Frauenrath Germany 12 384 0.8× 79 0.4× 121 2.5× 41 1.2× 23 0.7× 37 406
Mireia Pastó Spain 13 373 0.8× 183 1.0× 131 2.7× 20 0.6× 16 0.5× 18 433
Kazutaka Seki Japan 8 484 1.0× 142 0.8× 159 3.3× 18 0.5× 33 1.0× 8 511
Ayako Nakano Japan 7 377 0.8× 110 0.6× 108 2.3× 29 0.9× 7 0.2× 9 391
Wilfried Raimondi France 12 494 1.0× 116 0.7× 133 2.8× 18 0.5× 13 0.4× 13 511
Andrzej Zarecki Poland 9 281 0.6× 84 0.5× 35 0.7× 15 0.4× 26 0.8× 14 319

Countries citing papers authored by Thomas C. Stephens

Since Specialization
Citations

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

Fields of papers citing papers by Thomas C. Stephens

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas C. Stephens

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

All Works

10 of 10 papers shown
1.
Epton, Ryan G., Thomas C. Stephens, Lodi Mahendar, et al.. (2020). Evaluating the Viability of Successive Ring‐Expansions Based on Amino Acid and Hydroxyacid Side‐Chain Insertion. Chemistry - A European Journal. 26(55). 12674–12683. 23 indexed citations
2.
Stephens, Thomas C. & William P. Unsworth. (2019). Consecutive Ring-Expansion Reactions for the Iterative Assembly of Medium-Sized Rings and Macrocycles. Synlett. 31(2). 133–146. 23 indexed citations
3.
Rossi‐Ashton, James A., et al.. (2019). Internal Nucleophilic Catalyst Mediated Cyclisation/Ring Expansion Cascades for the Synthesis of Medium‐Sized Lactones and Lactams. Angewandte Chemie International Edition. 58(39). 13942–13947. 54 indexed citations
4.
Rossi‐Ashton, James A., et al.. (2019). Internal Nucleophilic Catalyst Mediated Cyclisation/Ring Expansion Cascades for the Synthesis of Medium‐Sized Lactones and Lactams. Angewandte Chemie. 131(39). 14080–14085. 22 indexed citations
5.
Stephens, Thomas C., et al.. (2018). A Coupling Approach for the Generation of α,α-Bis(enolate) Equivalents: Regioselective Synthesis of gem-Difunctionalized Ketones. Journal of the American Chemical Society. 140(6). 2036–2040. 74 indexed citations
6.
Ho, Hon Eong, Thomas C. Stephens, Thomas Payne, et al.. (2018). Merging π-Acid and Pd Catalysis: Dearomatizing Spirocyclization/Cross-Coupling Cascade Reactions of Alkyne-Tethered Aromatics. ACS Catalysis. 9(1). 504–510. 59 indexed citations
7.
Stephens, Thomas C., et al.. (2018). Iterative Assembly of Macrocyclic Lactones using Successive Ring Expansion Reactions. Chemistry - A European Journal. 24(52). 13947–13953. 47 indexed citations
8.
Stephens, Thomas C., et al.. (2017). Synthesis of Cyclic Peptide Mimetics by the Successive Ring Expansion of Lactams. Chemistry - A European Journal. 23(54). 13314–13318. 55 indexed citations
9.
Stephens, Thomas C. & Graham Pattison. (2017). Transition-Metal-Free Homologative Cross-Coupling of Aldehydes and Ketones with Geminal Bis(boron) Compounds. Organic Letters. 19(13). 3498–3501. 67 indexed citations
10.
Stephens, Thomas C., et al.. (2016). Ring‐Expansion Approach to Medium‐Sized Lactams and Analysis of Their Medicinal Lead‐Like Properties. Chemistry - A European Journal. 23(9). 2225–2230. 70 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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