K.S. Eccles

705 total citations
35 papers, 616 citations indexed

About

K.S. Eccles is a scholar working on Organic Chemistry, Physical and Theoretical Chemistry and Materials Chemistry. According to data from OpenAlex, K.S. Eccles has authored 35 papers receiving a total of 616 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Organic Chemistry, 15 papers in Physical and Theoretical Chemistry and 11 papers in Materials Chemistry. Recurrent topics in K.S. Eccles's work include Crystallography and molecular interactions (15 papers), Crystallization and Solubility Studies (10 papers) and Crystal structures of chemical compounds (9 papers). K.S. Eccles is often cited by papers focused on Crystallography and molecular interactions (15 papers), Crystallization and Solubility Studies (10 papers) and Crystal structures of chemical compounds (9 papers). K.S. Eccles collaborates with scholars based in Ireland, United Kingdom and Singapore. K.S. Eccles's co-authors include Simon E. Lawrence, Anita R. Maguire, L. Fábián, H.A. Moynihan, L. McCausland, S.P. Stokes, Gerard P. McGlacken, Doris E. Braun, Alan Ford and Abhijeet S. Sinha and has published in prestigious journals such as The Journal of Organic Chemistry, Tetrahedron and International Journal of Pharmaceutics.

In The Last Decade

K.S. Eccles

35 papers receiving 605 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
K.S. Eccles Ireland 15 311 272 263 166 97 35 616
Cristina Puigjaner Spain 13 175 0.6× 280 1.0× 194 0.7× 178 1.1× 102 1.1× 31 526
Matthew R. Scholfield United States 6 436 1.4× 167 0.6× 175 0.7× 187 1.1× 189 1.9× 6 652
Anilkumar Gunnam India 16 352 1.1× 158 0.6× 395 1.5× 104 0.6× 70 0.7× 26 593
Sarah J. Bethune United States 5 502 1.6× 171 0.6× 497 1.9× 114 0.7× 74 0.8× 6 641
J.T. Dunlap United States 5 471 1.5× 137 0.5× 448 1.7× 183 1.1× 83 0.9× 5 688
Gladis L. Sosa Argentina 11 363 1.2× 204 0.8× 144 0.5× 173 1.0× 58 0.6× 28 659
P.D. Chopade United States 10 384 1.2× 173 0.6× 238 0.9× 236 1.4× 43 0.4× 14 610
M.L. Cheney United States 7 607 2.0× 209 0.8× 554 2.1× 197 1.2× 89 0.9× 9 801
Carole Ouvrard France 9 308 1.0× 221 0.8× 178 0.7× 115 0.7× 64 0.7× 9 514
Daniel A. Adsmond United States 8 341 1.1× 187 0.7× 247 0.9× 201 1.2× 72 0.7× 10 523

Countries citing papers authored by K.S. Eccles

Since Specialization
Citations

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

Fields of papers citing papers by K.S. Eccles

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by K.S. Eccles. 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 K.S. Eccles. The network helps show where K.S. Eccles may publish in the future.

Co-authorship network of co-authors of K.S. Eccles

This figure shows the co-authorship network connecting the top 25 collaborators of K.S. Eccles. A scholar is included among the top collaborators of K.S. Eccles 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 K.S. Eccles. K.S. Eccles 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.
2.
Eccles, K.S., et al.. (2016). Methyl tetra-O-acetyl-α-d-glucopyranuronate: crystal structure and influence on the crystallisation of the β anomer. Carbohydrate Research. 425. 35–39. 4 indexed citations
3.
Gupta, Manoj, et al.. (2016). Cinchona-catalysed, Enantioselective Synthesis of β-Peroxycarboxylic Acids, β-Peroxyesters and β-Peroxyalcohols. Current Organic Chemistry. 20(24). 2633–2638. 2 indexed citations
4.
Eccles, K.S., et al.. (2015). Asymmetric Aldol–Tishchenko Reaction of Sulfinimines. Organic Letters. 17(22). 5642–5645. 16 indexed citations
5.
Stokes, S.P., Colin C. Seaton, K.S. Eccles, Anita R. Maguire, & Simon E. Lawrence. (2014). Insight into the Mechanism of Formation of Channel Hydrates via Templating. Crystal Growth & Design. 14(3). 1158–1166. 13 indexed citations
6.
Eccles, K.S., et al.. (2014). Halogen Bonding with Sulfur Functional Groups. Acta Crystallographica Section A Foundations and Advances. 70(a1). C651–C651. 1 indexed citations
7.
Eccles, K.S., et al.. (2014). Supramolecular stacking motifs in the solid state of amide and triazole derivatives of cellobiose. Carbohydrate Research. 388. 67–72. 1 indexed citations
8.
Maguire, Anita R., Catherine N. Slattery, Alan Ford, K.S. Eccles, & Simon E. Lawrence. (2014). Synthetic and Mechanistic Aspects on the Competition between C–H Insertion and Hydride Transfer in Copper-Mediated Transformations of α-Diazo-β-Keto Sulfones. Synlett. 25(4). 591–595. 3 indexed citations
9.
Moynihan, H.A., et al.. (2013). Hydrogen bonding in crystal forms of primary amide functionalised glucose and cellobiose. Carbohydrate Research. 374. 29–39. 8 indexed citations
10.
Eccles, K.S., et al.. (2013). Crystal Polymorphism of Methyl 2,3,4-tri-O-acetyl-1-O-(trichloroacetimidoyl)-α-d-glucopyranouronate. Journal of Chemical Crystallography. 43(3). 138–143. 3 indexed citations
11.
Eccles, K.S., et al.. (2013). Co-crystallisation through halogen bonding with racemic or enantiopure sulfinamides. CrystEngComm. 15(37). 7571–7571. 6 indexed citations
12.
Reen, F. Jerry, Sarah L. Clarke, Claire Legendre, et al.. (2012). Structure–function analysis of the C-3 position in analogues of microbial behavioural modulators HHQ and PQS. Organic & Biomolecular Chemistry. 10(44). 8903–8903. 35 indexed citations
13.
Eccles, K.S., S.P. Stokes, Noel M. O’Boyle, et al.. (2012). Utilizing Sulfoxide···Iodine Halogen Bonding for Cocrystallization. Crystal Growth & Design. 12(6). 2969–2977. 26 indexed citations
14.
Eccles, K.S., et al.. (2011). Preparation and characterisation of solid state forms of paracetamol-O-glucuronide. Carbohydrate Research. 349. 108–112. 10 indexed citations
15.
Eccles, K.S., Anita R. Maguire, Simon E. Lawrence, et al.. (2011). Characterisation, solubility and intrinsic dissolution behaviour of benzamide: dibenzyl sulfoxide cocrystal. International Journal of Pharmaceutics. 422(1-2). 24–32. 38 indexed citations
16.
Fábián, L., K.S. Eccles, H.A. Moynihan, et al.. (2011). Cocrystals of Fenamic Acids with Nicotinamide. Crystal Growth & Design. 11(8). 3522–3528. 108 indexed citations
17.
Eccles, K.S., et al.. (2011). The Use of Co-crystals for the Determination of Absolute Stereochemistry: An Alternative to Salt Formation. The Journal of Organic Chemistry. 76(4). 1159–1162. 14 indexed citations
18.
Eccles, K.S., et al.. (2011). Expanding the crystal landscape of isonicotinamide: concomitant polymorphism and co-crystallisation. CrystEngComm. 13(23). 6923–6923. 45 indexed citations
19.
20.
Eccles, K.S., S.P. Stokes, W.B. Jennings, et al.. (2010). Evaluation of the Bruker SMART X2S: crystallography for the nonspecialist?. Journal of Applied Crystallography. 44(1). 213–215. 33 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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