Peter Turner

490 total citations
11 papers, 409 citations indexed

About

Peter Turner is a scholar working on Organic Chemistry, Molecular Biology and Physiology. According to data from OpenAlex, Peter Turner has authored 11 papers receiving a total of 409 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Organic Chemistry, 3 papers in Molecular Biology and 1 paper in Physiology. Recurrent topics in Peter Turner's work include Synthetic Organic Chemistry Methods (5 papers), Catalytic Alkyne Reactions (4 papers) and Asymmetric Synthesis and Catalysis (3 papers). Peter Turner is often cited by papers focused on Synthetic Organic Chemistry Methods (5 papers), Catalytic Alkyne Reactions (4 papers) and Asymmetric Synthesis and Catalysis (3 papers). Peter Turner collaborates with scholars based in United Kingdom, Australia and Ireland. Peter Turner's co-authors include Tom D. Sheppard, Matthew G. Unthank, Shane M. Wilkinson, Michelle N. McDonnell, Louis M. Rendina, Hendra Gunosewoyo, Iain S. McGregor, Aurélie A. Boucher, Michael Kassiou and Melissa L. Barron and has published in prestigious journals such as Chemical Communications, The Journal of Organic Chemistry and Chemistry - A European Journal.

In The Last Decade

Peter Turner

11 papers receiving 402 citations

Peers

Peter Turner
Christopher E. Henry United States
Gaetano D’Anniballe Italy
John Paul Kilburn Denmark
Tony W. Dean United Kingdom
Steve F. Poon United States
Sofia Karlström Sweden
Eleni G. Andreadou Greece
Michael E. LeTourneau United States
G. B. Dharma Rao India
Deyong Su China
Christopher E. Henry United States
Peter Turner
Citations per year, relative to Peter Turner Peter Turner (= 1×) peers Christopher E. Henry

Countries citing papers authored by Peter Turner

Since Specialization
Citations

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

Fields of papers citing papers by Peter Turner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Peter Turner

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

All Works

11 of 11 papers shown
1.
Gibson, Samantha M., et al.. (2016). Intercepting the Gold‐Catalysed Meyer–Schuster Rearrangement by Controlled Protodemetallation: A Regioselective Hydration of Propargylic Alcohols. Advanced Synthesis & Catalysis. 358(9). 1519–1525. 25 indexed citations
2.
Wilkinson, Shane M., Hendra Gunosewoyo, Melissa L. Barron, et al.. (2014). The First CNS-Active Carborane: A Novel P2X7 Receptor Antagonist with Antidepressant Activity. ACS Chemical Neuroscience. 5(5). 335–339. 118 indexed citations
3.
Foster, Robert W., et al.. (2013). Gold catalysed synthesis of 3-alkoxyfurans at room temperature. Chemical Communications. 50(11). 1302–1304. 27 indexed citations
4.
Turner, Peter, et al.. (2012). Gold‐ and Silver‐Catalyzed Reactions of Propargylic Alcohols in the Presence of Protic Additives. Chemistry - A European Journal. 18(15). 4748–4758. 84 indexed citations
5.
Barbazanges, Marion, Christophe Meyer, Janine Cossy, & Peter Turner. (2011). Synthesis of 1,2‐Amino Alcohols by Sigmatropic Rearrangements of 3‐(N‐Tosylamino)allylic Alcohol Derivatives. Chemistry - A European Journal. 17(16). 4480–4495. 22 indexed citations
6.
Unthank, Matthew G., et al.. (2011). A General Procedure for the Synthesis of Enones via Gold-Catalyzed Meyer−Schuster Rearrangement of Propargylic Alcohols at Room Temperature. The Journal of Organic Chemistry. 76(5). 1479–1482. 81 indexed citations
7.
Whiting, Matthew, et al.. (2010). Selection and Development of the Manufacturing Route for EP1 Antagonist GSK269984B. Organic Process Research & Development. 14(4). 820–831. 15 indexed citations
8.
Bret, Guillaume, et al.. (2010). Development of the Route of Manufacture of an Oral H1−H3 Antagonist. Organic Process Research & Development. 15(1). 112–122. 8 indexed citations
9.
10.
Turner, Peter, Timothy J. Donohoe, & Rick Cousins. (2004). Rearrangement of pyrrolines derived from the Birch reduction of electron-deficient pyrroles: radical ring-expansion to substituted tetrahydropyridines. Chemical Communications. 1422–1422. 10 indexed citations
11.
Ridley, Damon D., et al.. (2003). Equine Metabolites of Norethandrolone: Synthesis of a Series of 19-Nor-17α-pregnanediols and 19-Nor-17α-pregnanetriols. Australian Journal of Chemistry. 56(8). 829–838. 12 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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2026