E.D. Savory

622 total citations
19 papers, 524 citations indexed

About

E.D. Savory is a scholar working on Organic Chemistry, Molecular Biology and Spectroscopy. According to data from OpenAlex, E.D. Savory has authored 19 papers receiving a total of 524 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Organic Chemistry, 10 papers in Molecular Biology and 4 papers in Spectroscopy. Recurrent topics in E.D. Savory's work include Asymmetric Synthesis and Catalysis (13 papers), Chemical Synthesis and Analysis (9 papers) and Synthetic Organic Chemistry Methods (8 papers). E.D. Savory is often cited by papers focused on Asymmetric Synthesis and Catalysis (13 papers), Chemical Synthesis and Analysis (9 papers) and Synthetic Organic Chemistry Methods (8 papers). E.D. Savory collaborates with scholars based in United Kingdom and United States. E.D. Savory's co-authors include Stephen G. Davies, Andrew D. Smith, Paul M. Roberts, Steven D. Bull, A. Christopher Garner, Rebecca L. Nicholson, James E. Thomson, Angela J. Russell, D.J. Watkin and Paul D. Price and has published in prestigious journals such as Chemical Communications, Tetrahedron and Organic Letters.

In The Last Decade

E.D. Savory

19 papers receiving 518 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
E.D. Savory United Kingdom 16 493 198 75 51 18 19 524
Joanna M. Szewczyk United States 8 485 1.0× 148 0.7× 73 1.0× 41 0.8× 26 1.4× 9 527
Jacqueline H. Smitrovich United States 16 760 1.5× 132 0.7× 148 2.0× 46 0.9× 24 1.3× 23 829
Hon‐Chung Tsui United States 10 515 1.0× 126 0.6× 116 1.5× 27 0.5× 29 1.6× 16 566
Carley Chandler Germany 5 491 1.0× 149 0.8× 136 1.8× 20 0.4× 18 1.0× 6 545
Shawn R. Hitchcock United States 15 638 1.3× 197 1.0× 203 2.7× 62 1.2× 28 1.6× 68 701
Jerome F. Hayes United Kingdom 18 538 1.1× 192 1.0× 83 1.1× 17 0.3× 23 1.3× 35 604
Ozora Kubo Japan 15 595 1.2× 219 1.1× 83 1.1× 20 0.4× 25 1.4× 29 641
Martin H. Osterhout United States 16 775 1.6× 140 0.7× 46 0.6× 45 0.9× 34 1.9× 24 825
Thomas M. Koenig United States 11 323 0.7× 117 0.6× 77 1.0× 44 0.9× 22 1.2× 15 432
Timothy J. Peelen United States 10 445 0.9× 116 0.6× 125 1.7× 19 0.4× 12 0.7× 12 479

Countries citing papers authored by E.D. Savory

Since Specialization
Citations

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

Fields of papers citing papers by E.D. Savory

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of E.D. Savory

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

All Works

19 of 19 papers shown
1.
Chernega, Alexander N., Stephen G. Davies, Ai M. Fletcher, et al.. (2010). Alkylation and aldol reactions of acyl derivatives of N-1-(1′-naphthyl)ethyl-O-tert-butylhydroxylamine: asymmetric synthesis of α-alkoxy-, α-substituted-β-alkoxy- and α,β-dialkoxyaldehydes. Tetrahedron. 66(23). 4167–4194. 7 indexed citations
2.
Davies, Stephen G., A. Christopher Garner, Rebecca L. Nicholson, et al.. (2009). Doubly diastereoselective [3,3]-sigmatropic aza-Claisen rearrangements. Organic & Biomolecular Chemistry. 7(12). 2604–2604. 22 indexed citations
3.
Davies, Stephen G., Rebecca L. Nicholson, Paul D. Price, et al.. (2009). Iodine-mediated ring-closing iodoamination with concomitant N-debenzylation for the asymmetric synthesis of polyhydroxylated pyrrolidines. Tetrahedron Asymmetry. 20(6-8). 758–772. 57 indexed citations
4.
5.
Claridge, Timothy D. W., Stephen G. Davies, M. E. C. POLYWKA, et al.. (2008). “Pure by NMR”?. Organic Letters. 10(23). 5433–5436. 39 indexed citations
6.
Aciro, C., Stephen G. Davies, A. Christopher Garner, et al.. (2008). Stereoselective functionalisation of SuperQuat enamides: asymmetric synthesis of homochiral 1,2-diols and α-benzyloxy carbonyl compounds. Tetrahedron. 64(39). 9320–9344. 27 indexed citations
7.
Bull, Steven D., Stephen G. Davies, A. Christopher Garner, et al.. (2006). SuperQuat 5,5-dimethyl-4-iso-propyloxazolidin-2-one as a mimic of Evans 4-tert-butyloxazolidin-2-one. Organic & Biomolecular Chemistry. 4(15). 2945–2945. 48 indexed citations
8.
Bull, Steven D., Stephen G. Davies, A. Christopher Garner, et al.. (2006). Enantiodiscrimination of racemic electrophiles by diketopiperazine enolates: asymmetric synthesis of methyl 2-amino-3-aryl-butanoates and 3-methyl-aspartates. Tetrahedron. 62(33). 7911–7925. 22 indexed citations
9.
Davies, Stephen G., A. Christopher Garner, Marcus J. C. Long, et al.. (2005). Kinetic resolution and parallel kinetic resolution of methyl (±)-5-alkyl-cyclopentene-1-carboxylates for the asymmetric synthesis of 5-alkyl-cispentacin derivatives. Organic & Biomolecular Chemistry. 3(15). 2762–2762. 55 indexed citations
10.
11.
Bull, Steven D., et al.. (2004). 2-Halo-diketopiperazines as chiral glycine cation equivalents. Tetrahedron Asymmetry. 15(24). 3989–4001. 14 indexed citations
12.
Davies, Stephen G., A. Christopher Garner, Rebecca L. Nicholson, et al.. (2003). Double diastereoselective [3,3]-sigmatropic aza-Claisen rearrangements. Chemical Communications. 2134–2134. 13 indexed citations
13.
Buñuel, Elena, Steven D. Bull, Stephen G. Davies, et al.. (2003). Asymmetric synthesis of substituted 1-aminocyclopropane-1-carboxylic acids via diketopiperazine methodology. Organic & Biomolecular Chemistry. 1(14). 2531–2542. 22 indexed citations
14.
Davies, Stephen G., et al.. (2003). Oxidative Functionalisation of SuperQuat Enamides: Asymmetric Synthesis of Homochiral 1,2 Diols. Synlett. 1659–1662. 22 indexed citations
15.
Bull, Steven D., Stephen G. Davies, David J. Fox, et al.. (2002). Asymmetric synthesis of β-pyridyl-β-amino acid derivatives. Journal of the Chemical Society Perkin Transactions 1. 1858–1868. 27 indexed citations
16.
Bull, Steven D., et al.. (2002). Chiral glycine cation equivalents: N-acyliminium species derived from diketopiperazines. Journal of the Chemical Society Perkin Transactions 1. 2442–2448. 17 indexed citations
17.
Bew, Sean P., Steven D. Bull, Stephen G. Davies, E.D. Savory, & D.J. Watkin. (2002). Rearrangements and racemisation during the synthesis of l-serine derived oxazolidin-2-ones. Tetrahedron. 58(46). 9387–9401. 27 indexed citations
18.
Bull, Steven D., Stephen G. Davies, Paul M. Roberts, E.D. Savory, & Andrew D. Smith. (2002). Asymmetric synthesis of homochiral differentially protected bis-β-amino acid scaffolds. Tetrahedron. 58(23). 4629–4642. 22 indexed citations
19.

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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