David A. Chaplin

515 total citations
16 papers, 395 citations indexed

About

David A. Chaplin is a scholar working on Organic Chemistry, Molecular Biology and Spectroscopy. According to data from OpenAlex, David A. Chaplin has authored 16 papers receiving a total of 395 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Organic Chemistry, 8 papers in Molecular Biology and 5 papers in Spectroscopy. Recurrent topics in David A. Chaplin's work include Enzyme Catalysis and Immobilization (5 papers), Carbohydrate Chemistry and Synthesis (4 papers) and Analytical Chemistry and Chromatography (4 papers). David A. Chaplin is often cited by papers focused on Enzyme Catalysis and Immobilization (5 papers), Carbohydrate Chemistry and Synthesis (4 papers) and Analytical Chemistry and Chromatography (4 papers). David A. Chaplin collaborates with scholars based in United Kingdom, Czechia and India. David A. Chaplin's co-authors include Kevin Burgess, Matthias Breuning, Dieter Seebàch, Keiji Matsuda, Georg Jaeschke, Gerhard Bringmann, Alan D. Elbein, Gerard A. Potter, Stephen J. Taylor and Nicholas Johnson and has published in prestigious journals such as Chemical Communications, The Journal of Organic Chemistry and Tetrahedron.

In The Last Decade

David A. Chaplin

16 papers receiving 370 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David A. Chaplin United Kingdom 13 295 189 67 49 39 16 395
Daniel Mink Netherlands 7 292 1.0× 276 1.5× 74 1.1× 19 0.4× 62 1.6× 10 449
Michael C. Hillier United States 14 409 1.4× 199 1.1× 53 0.8× 39 0.8× 30 0.8× 21 521
Kevin E. Henegar United States 12 267 0.9× 137 0.7× 49 0.7× 36 0.7× 19 0.5× 20 372
Masaya Ikunaka Japan 15 279 0.9× 222 1.2× 74 1.1× 21 0.4× 107 2.7× 29 466
Jayachandra P. Reddy United States 14 458 1.6× 165 0.9× 49 0.7× 101 2.1× 18 0.5× 19 594
Fausta Ulgheri Italy 11 358 1.2× 128 0.7× 60 0.9× 28 0.6× 29 0.7× 24 408
Martin E. Fox United Kingdom 14 433 1.5× 129 0.7× 138 2.1× 34 0.7× 17 0.4× 27 502
Andreas Job Germany 6 419 1.4× 143 0.8× 82 1.2× 52 1.1× 24 0.6× 9 468
M. Serajul Haque United States 12 479 1.6× 175 0.9× 75 1.1× 28 0.6× 32 0.8× 17 575
Stephen E. Shanahan United Kingdom 8 307 1.0× 114 0.6× 105 1.6× 43 0.9× 14 0.4× 13 422

Countries citing papers authored by David A. Chaplin

Since Specialization
Citations

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

Fields of papers citing papers by David A. Chaplin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David A. Chaplin. 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 David A. Chaplin. The network helps show where David A. Chaplin may publish in the future.

Co-authorship network of co-authors of David A. Chaplin

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

All Works

16 of 16 papers shown
1.
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
2.
Chaplin, David A., Martin E. Fox, & Sebastian H. B. Kroll. (2014). Dynamic kinetic resolution of dehydrocoronamic acid. Chemical Communications. 50(44). 5858–5860. 14 indexed citations
3.
Bergeron, Sophie, et al.. (2006). Nitrilase-Catalysed Desymmetrisation of 3-Hydroxyglutaronitrile:  Preparation of a Statin Side-Chain Intermediate. Organic Process Research & Development. 10(3). 661–665. 57 indexed citations
4.
Chaplin, David A., Paul Harrison, Julian P. Henschke, et al.. (2002). Industrially Viable Syntheses of Highly Enantiomerically Enriched 1-Aryl Alcohols via Asymmetric Hydrogenation. Organic Process Research & Development. 7(1). 89–94. 35 indexed citations
5.
Lloyd, Richard C., et al.. (2002). Chemoenzymatic Synthesis of the Four Diastereoisomers of 4-Hydroxypipecolic Acid from N-Acetyl-(R,S)-allylglycine:  Chiral Scaffolds for Drug Discovery. Organic Process Research & Development. 6(6). 762–766. 10 indexed citations
6.
Smith, Mark E. B., et al.. (2001). Highly selective directed hydrogenation of enantiopure 4-( tert -butoxycarbonylamino)cyclopent-1-enecarboxylic acid methyl esters. Tetrahedron Letters. 42(7). 1347–1350. 20 indexed citations
7.
Smith, Mark E. B., Richard C. Lloyd, Stephen J. Taylor, et al.. (2001). An efficient route to all eight stereoisomers of a tri-functionalised cyclopentane scaffold for drug discovery. Tetrahedron Asymmetry. 12(5). 703–705. 18 indexed citations
8.
Chaplin, David A., et al.. (1998). Dynamic diastereomeric salt resolution of narwedine and its transformation to (−)-galanthamine. Tetrahedron Letters. 39(37). 6777–6780. 27 indexed citations
9.
Chaplin, David A., et al.. (1997). A concise, scaleable synthesis of narwedine. Tetrahedron Letters. 38(45). 7931–7932. 19 indexed citations
10.
Seebàch, Dieter, Georg Jaeschke, Keiji Matsuda, et al.. (1997). Resolution of racemic carboxylic acid derivatives by Ti-TADDOLate mediated esterification reactions—A general method for the preparation of enantiopure compounds. Tetrahedron. 53(22). 7539–7556. 87 indexed citations
11.
12.
Burgess, Kevin, et al.. (1994). Preparation of a Deoxynojirimycin Analog Containing an Imidazole Ring. Heterocycles. 37(2). 673–673. 14 indexed citations
13.
Burgess, Kevin & David A. Chaplin. (1992). An asymmetric synthesis of D-1,6-Diepicastanospermine. Tetrahedron Letters. 33(41). 6077–6080. 19 indexed citations
14.
Burgess, Kevin, et al.. (1992). A route to several stereoisomers of castanospermine. The Journal of Organic Chemistry. 57(4). 1103–1109. 34 indexed citations
15.
Chaplin, David A., David H. G. Crout, Stephen Bornemann, D. W. Hutchinson, & Riaz Khan. (1992). Conversion of 2-acetamido-2-deoxy-β-D-glucopyranose (N-acetylglucosamine) into 2-acetamido-2-deoxy-β-D-galactopyranose (N-acetylgalactosamine) using a biotransformation to generate a selectively deprotected substrate for SN2 inversion. Journal of the Chemical Society Perkin Transactions 1. 235–237. 22 indexed citations
16.
Chaplin, David A., David H. G. Crout, D. W. Hutchinson, Oliver W. Howarth, & Riaz Khan. (1991). Perdeuterioacetylation with combined NMR and MS analysis as a method for determining the evolution of individual hydrolysis products during regioselective enzymatic hydrolysis of glucose pentaacetate. Catalysis Letters. 9(1-2). 71–83. 5 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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