James Rae

645 total citations
8 papers, 579 citations indexed

About

James Rae is a scholar working on Organic Chemistry, Pharmacology and Spectroscopy. According to data from OpenAlex, James Rae has authored 8 papers receiving a total of 579 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Organic Chemistry, 1 paper in Pharmacology and 1 paper in Spectroscopy. Recurrent topics in James Rae's work include Organoboron and organosilicon chemistry (7 papers), Catalytic Cross-Coupling Reactions (6 papers) and Catalytic C–H Functionalization Methods (3 papers). James Rae is often cited by papers focused on Organoboron and organosilicon chemistry (7 papers), Catalytic Cross-Coupling Reactions (6 papers) and Catalytic C–H Functionalization Methods (3 papers). James Rae collaborates with scholars based in United Kingdom and France. James Rae's co-authors include David J. Procter, K. -S. Yeung, Vittorio Pace, Alexander P. Pulis, Rebecca E. Ruscoe, Joseph J. W. McDouall, Hassan Y. Harb, Joanna Wencel‐Delord, Johanna Frey and Françoise Colobert and has published in prestigious journals such as Angewandte Chemie International Edition, Chemical Communications and ACS Catalysis.

In The Last Decade

James Rae

8 papers receiving 562 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
James Rae United Kingdom 8 567 123 78 44 26 8 579
Shengbiao Tang China 18 733 1.3× 173 1.4× 74 0.9× 29 0.7× 40 1.5× 46 747
Pu‐Fan Qian China 11 510 0.9× 106 0.9× 31 0.4× 76 1.7× 18 0.7× 15 523
Jiguo Ma China 6 323 0.6× 119 1.0× 94 1.2× 34 0.8× 32 1.2× 9 347
David Kossler Switzerland 8 500 0.9× 197 1.6× 45 0.6× 9 0.2× 21 0.8× 12 529
Huaanzi Hu China 9 436 0.8× 80 0.7× 53 0.7× 37 0.8× 22 0.8× 11 441
Alexa Torelli Canada 10 625 1.1× 174 1.4× 56 0.7× 14 0.3× 47 1.8× 12 639
Melvin De Jesús Puerto Rico 11 290 0.5× 140 1.1× 179 2.3× 26 0.6× 14 0.5× 20 352
Su Yu United States 12 435 0.8× 100 0.8× 61 0.8× 31 0.7× 25 1.0× 27 453
Mengyao Tang China 13 680 1.2× 211 1.7× 52 0.7× 72 1.6× 16 0.6× 22 692
Anirudra Paul United States 11 612 1.1× 154 1.3× 73 0.9× 8 0.2× 31 1.2× 16 629

Countries citing papers authored by James Rae

Since Specialization
Citations

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

Fields of papers citing papers by James Rae

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of James Rae

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

All Works

8 of 8 papers shown
1.
Rae, James, et al.. (2018). Synthesis of Axially Chiral C–N Scaffolds via Asymmetric Coupling with Enantiopure Sulfinyl Iodanes. ACS Catalysis. 8(4). 2805–2809. 78 indexed citations
2.
Yeung, K. -S., Rebecca E. Ruscoe, James Rae, Alexander P. Pulis, & David J. Procter. (2016). Enantioselective Generation of Adjacent Stereocenters in a Copper‐Catalyzed Three‐Component Coupling of Imines, Allenes, and Diboranes. Angewandte Chemie. 128(39). 12091–12095. 50 indexed citations
3.
Yeung, K. -S., Rebecca E. Ruscoe, James Rae, Alexander P. Pulis, & David J. Procter. (2016). Enantioselective Generation of Adjacent Stereocenters in a Copper‐Catalyzed Three‐Component Coupling of Imines, Allenes, and Diboranes. Angewandte Chemie International Edition. 55(39). 11912–11916. 137 indexed citations
4.
Rae, James, K. -S. Yeung, Joseph J. W. McDouall, & David J. Procter. (2015). Copper‐Catalyzed Borylative Cross‐Coupling of Allenes and Imines: Selective Three‐Component Assembly of Branched Homoallyl Amines. Angewandte Chemie International Edition. 55(3). 1102–1107. 98 indexed citations
5.
Rae, James, K. -S. Yeung, Joseph J. W. McDouall, & David J. Procter. (2015). Copper‐Catalyzed Borylative Cross‐Coupling of Allenes and Imines: Selective Three‐Component Assembly of Branched Homoallyl Amines. Angewandte Chemie. 128(3). 1114–1119. 32 indexed citations
6.
Rae, James, et al.. (2014). Cu(I)–NHC‐Catalyzed Silylation of Allenes: Diastereoselective Three‐Component Coupling with Aldehydes. Chemistry - A European Journal. 20(41). 13143–13145. 45 indexed citations
7.
Pace, Vittorio, James Rae, Hassan Y. Harb, & David J. Procter. (2013). NHC–Cu(i) catalysed asymmetric conjugate silyl transfer to unsaturated lactones: application in kinetic resolution. Chemical Communications. 49(45). 5150–5150. 57 indexed citations
8.
Pace, Vittorio, James Rae, & David J. Procter. (2013). Cu(I)–NHC Catalyzed Asymmetric Silyl Transfer to Unsaturated Lactams and Amides. Organic Letters. 16(2). 476–479. 82 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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