Martin E. Fox

685 total citations
27 papers, 502 citations indexed

About

Martin E. Fox is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, Martin E. Fox has authored 27 papers receiving a total of 502 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Organic Chemistry, 10 papers in Molecular Biology and 9 papers in Inorganic Chemistry. Recurrent topics in Martin E. Fox's work include Asymmetric Synthesis and Catalysis (13 papers), Asymmetric Hydrogenation and Catalysis (9 papers) and Synthetic Organic Chemistry Methods (7 papers). Martin E. Fox is often cited by papers focused on Asymmetric Synthesis and Catalysis (13 papers), Asymmetric Hydrogenation and Catalysis (9 papers) and Synthetic Organic Chemistry Methods (7 papers). Martin E. Fox collaborates with scholars based in United Kingdom, United States and India. Martin E. Fox's co-authors include Ian C. Lennon, Joseph P. Marino, Chi Kong Li, Larry E. Overman, Mark Jackson, Mervyn Thompson, Andrew B. Holmes, Simon Woodward, Graham Meek and Ian T. Forbes and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Chemical Communications.

In The Last Decade

Martin E. Fox

26 papers receiving 487 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Martin E. Fox United Kingdom 14 433 138 129 34 26 27 502
Philippe Delair France 16 507 1.2× 63 0.5× 145 1.1× 30 0.9× 17 0.7× 23 563
Fausta Ulgheri Italy 11 358 0.8× 60 0.4× 128 1.0× 28 0.8× 21 0.8× 24 408
Dalian Zhao United States 14 331 0.8× 81 0.6× 152 1.2× 20 0.6× 44 1.7× 20 448
Darren Stead United Kingdom 10 527 1.2× 107 0.8× 132 1.0× 18 0.5× 11 0.4× 18 587
Yoshitaka Araki Japan 14 432 1.0× 125 0.9× 127 1.0× 29 0.9× 12 0.5× 28 559
Chan‐Mo Yu South Korea 20 920 2.1× 210 1.5× 141 1.1× 30 0.9× 19 0.7× 62 974
Thomas M. Razler United States 11 494 1.1× 79 0.6× 107 0.8× 58 1.7× 20 0.8× 19 545
Neil G. Andersen Canada 15 714 1.6× 274 2.0× 160 1.2× 23 0.7× 29 1.1× 18 798
Arun A. Narine Germany 9 834 1.9× 160 1.2× 196 1.5× 18 0.5× 21 0.8× 14 876
Andrew R. Pape United Kingdom 9 782 1.8× 157 1.1× 97 0.8× 21 0.6× 14 0.5× 10 872

Countries citing papers authored by Martin E. Fox

Since Specialization
Citations

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

Fields of papers citing papers by Martin E. Fox

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martin E. Fox

This figure shows the co-authorship network connecting the top 25 collaborators of Martin E. Fox. A scholar is included among the top collaborators of Martin E. Fox 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 Martin E. Fox. Martin E. Fox 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.
Singh, Manpreet, Vidavalur Siddaiah, Javed Iqbal, et al.. (2017). A diastereoselective synthesis of boceprevir's gem-dimethyl bicyclic [3.1.0] proline intermediate from an insecticide ingredient cis-cypermethric acid. Tetrahedron. 73(30). 4285–4294. 9 indexed citations
2.
Bernardi, Luca, Mariafrancesca Fochi, Martin E. Fox, et al.. (2015). Organocatalytic Asymmetric Conjugate Additions to Cyclopent‐1‐enecarbaldehyde: A Critical Assessment of Organocatalytic Approaches towards the Telaprevir Bicyclic Core. Chemistry - A European Journal. 21(52). 19208–19222. 16 indexed citations
3.
Chaplin, David A., et al.. (2015). An Enantioselective Formal Synthesis of Montelukast Sodium. The Journal of Organic Chemistry. 80(8). 3891–3901. 13 indexed citations
4.
Fox, Martin E., et al.. (2011). Large-Scale Synthesis of a Substituted d-Phenylalanine Using Asymmetric Hydrogenation. Organic Process Research & Development. 15(5). 1163–1171. 13 indexed citations
5.
Woodward, Simon, et al.. (2011). Bis‐Sulfamyl Imines: Potent Substrates for Asymmetric Additions of Arylboroxines under Rhodium Catalysis. Advanced Synthesis & Catalysis. 353(6). 903–906. 25 indexed citations
6.
Anson, M., Hugh Clark, P. Andrew Evans, et al.. (2011). Complementary Syntheses of N,O-Protected-(S)-2-methylserine on a Multikilogram Scale. Organic Process Research & Development. 15(2). 389–397. 12 indexed citations
7.
Fox, Martin E., Ian C. Lennon, & Vittorio Farina. (2007). Catalytic asymmetric synthesis of ethyl (1R,2S)-dehydrocoronamate. Tetrahedron Letters. 48(6). 945–948. 22 indexed citations
8.
Fox, Martin E., Mark Jackson, Ian C. Lennon, Jerzy Klosin, & Khalil A. Abboud. (2007). Bis-(2,5-diphenylphospholanes) with sp2 Carbon Linkers:  Synthesis and Application in Asymmetric Hydrogenation. The Journal of Organic Chemistry. 73(3). 775–784. 30 indexed citations
9.
Fox, Martin E. & Raymond McCague. (2005). Identifying stereoisomers of the asymmetric hydrogenation catalyst [Me‐BPE‐Rh(COD)]+BF. Chirality. 17(4). 177–185.
10.
Fox, Martin E., Mark Jackson, Ian C. Lennon, & Raymond McCague. (2005). A Convergent Synthesis of the 11-Oxa Prostaglandin Analogue AL-12182. The Journal of Organic Chemistry. 70(4). 1227–1236. 11 indexed citations
11.
Lennon, Ian C., et al.. (2005). A Convenient and Scaleable Synthesis of 11,12-Diamino-9,10-dihydro-9,10-ethanoanthracene and Its Enantiomers. Synthesis. 3196–3198. 4 indexed citations
12.
Boulton, Lee T., Martin E. Fox, Paul B. Hodgson, & Ian C. Lennon. (2004). Zinc-mediated intramolecular acyl and imino transfer reactions of aryl iodides. Tetrahedron Letters. 46(6). 983–986. 5 indexed citations
13.
Fox, Martin E., et al.. (2004). An efficient, palladium-catalyzed, enantioselective synthesis of (2 R )-3-butene-1,2-diol and its use in highly selective Heck reactions. Proceedings of the National Academy of Sciences. 101(15). 5396–5399. 11 indexed citations
14.
Fox, Martin E., Mark Jackson, Ian C. Lennon, Raymond McCague, & Julian S. Parratt. (2002). An Enantioconvergent Synthesis of (R)-4-Aryloxy-1-butyne-3-ols for Prostanoid Side Chains. Advanced Synthesis & Catalysis. 344(1). 50–50. 4 indexed citations
15.
Boulton, Lee T., Martin E. Fox, Mark Jackson, et al.. (2002). Synthesis of the Potent Antiglaucoma Agent, Travoprost. Organic Process Research & Development. 6(2). 138–145. 24 indexed citations
16.
17.
Fox, Martin E., Chi Kong Li, Joseph P. Marino, & Larry E. Overman. (1999). Enantiodivergent Total Syntheses of (+)- and (−)-Scopadulcic Acid A. Journal of the American Chemical Society. 121(23). 5467–5480. 112 indexed citations
18.
Fox, Martin E., Andrew B. Holmes, Ian T. Forbes, & Mervyn Thompson. (1994). N-alkenyl nitrone dipolar cycloaddition routes to piperidines and indolizidines. Part 7. Hydroxylamine–alkyne cyclisations. Formation of cyclic nitrones and application to the synthesis of the proposed structure for (±)-acacialactam. Journal of the Chemical Society Perkin Transactions 1. 3379–3395. 19 indexed citations
19.
Fox, Martin E., Andrew B. Holmes, Ian T. Forbes, Mervyn Thompson, & Joseph W. Ziller. (1992). Hydroxylamine-alkyne cyclisations. Synthesis of the seven-membered lactam structure proposed for (±)-acacialactam. Tetrahedron Letters. 33(48). 7425–7428. 10 indexed citations
20.
Fox, Martin E., Andrew B. Holmes, Ian T. Forbes, & Mervyn Thompson. (1992). Hydroxylamine-alkyne cyclisations. A new method for the synthesis of cyclic nitrones. Tetrahedron Letters. 33(48). 7421–7424. 11 indexed citations

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