Paul R. Blakemore

3.2k total citations · 2 hit papers
59 papers, 2.6k citations indexed

About

Paul R. Blakemore is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, Paul R. Blakemore has authored 59 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Organic Chemistry, 9 papers in Molecular Biology and 8 papers in Pharmacology. Recurrent topics in Paul R. Blakemore's work include Asymmetric Synthesis and Catalysis (20 papers), Synthetic Organic Chemistry Methods (14 papers) and Coordination Chemistry and Organometallics (13 papers). Paul R. Blakemore is often cited by papers focused on Asymmetric Synthesis and Catalysis (20 papers), Synthetic Organic Chemistry Methods (14 papers) and Coordination Chemistry and Organometallics (13 papers). Paul R. Blakemore collaborates with scholars based in United States, United Kingdom and Germany. Paul R. Blakemore's co-authors include Philip Kocieński, Andrew Morley, W.J. Cole, James D. White, Matthew S. Burge, Lev N. Zakharov, Stephen P. Marsden, Xun Sun, C.A. Kilner and Kenneth W. Muir and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Chemical Communications.

In The Last Decade

Paul R. Blakemore

54 papers receiving 2.5k citations

Hit Papers

A Stereoselective Synthesis oftrans-1,2-Disubstituted Alk... 1998 2026 2007 2016 1998 2002 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Paul R. Blakemore United States 24 2.2k 523 410 290 177 59 2.6k
Jun Ishihara Japan 28 1.8k 0.8× 666 1.3× 298 0.7× 306 1.1× 240 1.4× 145 2.4k
Mukund K. Gurjar India 26 2.1k 1.0× 908 1.7× 371 0.9× 339 1.2× 130 0.7× 164 2.4k
Deukjoon Kim South Korea 29 1.7k 0.8× 537 1.0× 355 0.9× 347 1.2× 139 0.8× 108 2.3k
Ken‐ichi Takao Japan 27 2.1k 0.9× 562 1.1× 397 1.0× 422 1.5× 99 0.6× 125 2.5k
Fuyuhiko Matsuda Japan 25 1.3k 0.6× 465 0.9× 298 0.7× 291 1.0× 151 0.9× 101 1.8k
Taotao Ling United States 24 1.3k 0.6× 576 1.1× 330 0.8× 324 1.1× 138 0.8× 47 2.0k
Yoshiki Morimoto Japan 24 1.2k 0.5× 381 0.7× 463 1.1× 323 1.1× 95 0.5× 111 1.6k
Masaya Nakata Japan 29 2.1k 0.9× 911 1.7× 403 1.0× 631 2.2× 101 0.6× 149 2.6k
David Dı́ez Spain 26 1.8k 0.8× 1.0k 2.0× 596 1.5× 329 1.1× 207 1.2× 206 2.8k
Bo Liu China 30 2.1k 1.0× 862 1.6× 435 1.1× 370 1.3× 294 1.7× 171 3.0k

Countries citing papers authored by Paul R. Blakemore

Since Specialization
Citations

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

Fields of papers citing papers by Paul R. Blakemore

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Paul R. Blakemore. 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 Paul R. Blakemore. The network helps show where Paul R. Blakemore may publish in the future.

Co-authorship network of co-authors of Paul R. Blakemore

This figure shows the co-authorship network connecting the top 25 collaborators of Paul R. Blakemore. A scholar is included among the top collaborators of Paul R. Blakemore 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 Paul R. Blakemore. Paul R. Blakemore 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.
Zakharov, Lev N., et al.. (2024). Total Synthesis of Chalaniline A: An Aminofulvene Fused Chromone from Vorinostat-Treated Fungus Chalara sp. 6661. The Journal of Organic Chemistry. 89(19). 14601–14605.
2.
Cao, Yang, Yang Huang, & Paul R. Blakemore. (2022). Synthesis of Thioalkynes by Desilylative Sonogashira Cross‐Coupling of Aryl Iodides and 1‐Methylthio‐2‐(trimethylsilyl)ethyne. European Journal of Organic Chemistry. 2022(34). 8 indexed citations
3.
Blakemore, Paul R., et al.. (2021). Stereospecific Synthesis of Conjugated Dienes by Carbenoid Eliminative Cross‐Coupling Using Lithiated Allylic Carbamates. European Journal of Organic Chemistry. 2021(35). 4932–4937. 1 indexed citations
5.
Zhang, Yang, Gerd Bobe, Johana S. Revel, et al.. (2019). Improvements in Metabolic Syndrome by Xanthohumol Derivatives Are Linked to Altered Gut Microbiota and Bile Acid Metabolism. Molecular Nutrition & Food Research. 64(1). e1900789–e1900789. 44 indexed citations
6.
Sephton, Selena Milicevic, Alexander Herrmann, James A. Strother, et al.. (2019). Biological evaluation of molecules of the azaBINOL class as antiviral agents: Inhibition of HIV-1 RNase H activity by 7-isopropoxy-8-(naphth-1-yl)quinoline. Bioorganic & Medicinal Chemistry. 27(16). 3595–3604. 26 indexed citations
7.
Blakemore, Paul R. & Reinhard W. Hoffmann. (2017). Olefin‐Bildung durch eliminierende Dimerisierung und eliminierende Kreuzkupplung von Carbenoiden: eine stereochemische Herausforderung. Angewandte Chemie. 130(2). 396–413. 11 indexed citations
8.
Blakemore, Paul R. & Reinhard W. Hoffmann. (2017). Formation of Olefins by Eliminative Dimerization and Eliminative Cross‐Coupling of Carbenoids: A Stereochemical Exercise. Angewandte Chemie International Edition. 57(2). 390–407. 16 indexed citations
10.
Place, Benjamin J., et al.. (2014). Trace analysis of surfactants in Corexit oil dispersant formulations and seawater. Deep Sea Research Part II Topical Studies in Oceanography. 129. 273–281. 47 indexed citations
12.
Zakharov, Lev N., et al.. (2013). Investigation of Functionalized α‐Chloroalkyllithiums for a Stereospecific Reagent‐Controlled Homologation Approach to the Analgesic Alkaloid (−)‐Epibatidine. Chemistry - A European Journal. 19(48). 16342–16356. 30 indexed citations
13.
Blakemore, Paul R., et al.. (2011). Stereocontrolled Generation of α-Metalated S,O-Acetals by Sulfoxide-Ligand Exchange from Cyclic Dithioorthoformate Monooxides. Organometallics. 31(1). 19–22. 10 indexed citations
14.
Sephton, Mark A., et al.. (2010). Spontaneous symmetry breaking during interrupted crystallization of an axially chiral amino acid derivative. Chemical Communications. 46(12). 2094–2094. 13 indexed citations
15.
Blakemore, Paul R., Matthew S. Burge, & Mark A. Sephton. (2007). Competing reaction pathways from α-halo-α-protioalkyl aryl sulfoxides initiated by organometallic reagents. Tetrahedron Letters. 48(23). 3999–4002. 15 indexed citations
16.
Blakemore, Paul R., et al.. (2005). Total Synthesis of Polycavernoside A (I), a Lethal Toxin of the Red Alga Polycavernosa tsudai.. ChemInform. 36(49). 1 indexed citations
17.
Blakemore, Paul R., et al.. (2005). Ethyl (benzothiazol-2-ylsulfonyl)acetate: a new reagent for the stereoselective synthesis of α,β-unsaturated esters from aldehydes. Organic & Biomolecular Chemistry. 3(8). 1365–1368. 50 indexed citations
18.
Blakemore, Paul R.. (2002). The modified Julia olefination: alkene synthesis via the condensation of metallated heteroarylalkylsulfones with carbonyl compounds. Journal of the Chemical Society Perkin Transactions 1. 2563–2585. 578 indexed citations breakdown →
19.
Blakemore, Paul R., Volker Schulze, & James D. White. (2000). Asymmetric synthesis of (+)-loline. Chemical Communications. 1263–1264. 22 indexed citations
20.
Blakemore, Paul R.. (1999). The Modified Julia Olefination in Vitamin D2 Synthesis. Synthesis. 1999(7). 1209–1215. 36 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026