Christopher G. Newton

3.0k total citations · 1 hit paper
52 papers, 2.5k citations indexed

About

Christopher G. Newton is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, Christopher G. Newton has authored 52 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Organic Chemistry, 12 papers in Molecular Biology and 7 papers in Pharmacology. Recurrent topics in Christopher G. Newton's work include Asymmetric Synthesis and Catalysis (11 papers), Synthesis and Biological Evaluation (7 papers) and Chemical Synthesis and Analysis (6 papers). Christopher G. Newton is often cited by papers focused on Asymmetric Synthesis and Catalysis (11 papers), Synthesis and Biological Evaluation (7 papers) and Chemical Synthesis and Analysis (6 papers). Christopher G. Newton collaborates with scholars based in United Kingdom, Australia and United States. Christopher G. Newton's co-authors include Nicolai Cramer, Caio C. Oliveira, Shouguo Wang, Christopher A. Ramsden, David Kossler, Matthew D. Wodrich, Michael S. Sherburn, E. Lunt, Malcolm F. G. Stevens and John A. Hickman and has published in prestigious journals such as Chemical Reviews, Journal of the American Chemical Society and Angewandte Chemie International Edition.

In The Last Decade

Christopher G. Newton

50 papers receiving 2.4k citations

Hit Papers

Catalytic Enantioselective Transformations Involving C–H ... 2017 2026 2020 2023 2017 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christopher G. Newton United Kingdom 21 2.1k 490 392 201 118 52 2.5k
Shi‐Wei Luo China 34 3.5k 1.7× 749 1.5× 596 1.5× 222 1.1× 162 1.4× 76 4.0k
Frederick A. Luzzio United States 21 1.4k 0.7× 282 0.6× 571 1.5× 144 0.7× 43 0.4× 69 1.8k
Hyun‐Joon Ha South Korea 30 2.4k 1.1× 281 0.6× 732 1.9× 151 0.8× 45 0.4× 157 3.0k
Kian L. Tan United States 27 1.9k 0.9× 676 1.4× 530 1.4× 59 0.3× 49 0.4× 50 2.4k
Guido Koch Switzerland 25 1.4k 0.7× 438 0.9× 573 1.5× 76 0.4× 32 0.3× 54 1.9k
Christopher J. Borths United States 11 1.7k 0.8× 448 0.9× 386 1.0× 120 0.6× 28 0.2× 17 2.0k
Kap‐Sun Yeung United States 22 2.1k 1.0× 481 1.0× 387 1.0× 107 0.5× 40 0.3× 46 2.6k
Christopher J. Dinsmore United States 25 1.3k 0.6× 188 0.4× 689 1.8× 71 0.4× 72 0.6× 47 1.8k
Francis Gosselin United States 28 1.9k 0.9× 635 1.3× 822 2.1× 118 0.6× 38 0.3× 104 2.5k
F. G. West Canada 43 4.0k 1.9× 338 0.7× 861 2.2× 108 0.5× 81 0.7× 175 4.7k

Countries citing papers authored by Christopher G. Newton

Since Specialization
Citations

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

Fields of papers citing papers by Christopher G. Newton

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christopher G. Newton. 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 Christopher G. Newton. The network helps show where Christopher G. Newton may publish in the future.

Co-authorship network of co-authors of Christopher G. Newton

This figure shows the co-authorship network connecting the top 25 collaborators of Christopher G. Newton. A scholar is included among the top collaborators of Christopher G. Newton 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 Christopher G. Newton. Christopher G. Newton 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.
Newton, Christopher G., et al.. (2025). Hetero-Diels–Alder reactions of (isobenzo)furans. Organic & Biomolecular Chemistry. 23(43). 9781–9796.
2.
Wheeler, Steven E., et al.. (2025). Ketenimines as Aza-Dienophiles. Journal of the American Chemical Society. 147(7). 6087–6094. 3 indexed citations
3.
Newton, Christopher G., et al.. (2022). Ring Forming Approaches to para-Quinones: Toward a General Diels–Alder Disconnection. Synlett. 33(15). 1473–1480. 2 indexed citations
4.
Newton, Christopher G., et al.. (2019). A Broad‐Spectrum Synthesis of Tetravinylethylenes. Chemistry - A European Journal. 25(16). 4072–4076. 7 indexed citations
5.
Newton, Christopher G., et al.. (2018). Axially Chiral Dibenzazepinones by a Palladium(0)‐Catalyzed Atropo‐enantioselective C−H Arylation. Angewandte Chemie. 130(34). 11206–11210. 48 indexed citations
6.
Newton, Christopher G., Duc N. Tran, Matthew D. Wodrich, & Nicolai Cramer. (2017). One‐Step Multigram‐Scale Biomimetic Synthesis of Psiguadial B. Angewandte Chemie. 129(44). 13964–13968. 5 indexed citations
7.
Newton, Christopher G., Duc N. Tran, Matthew D. Wodrich, & Nicolai Cramer. (2017). One‐Step Multigram‐Scale Biomimetic Synthesis of Psiguadial B. Angewandte Chemie International Edition. 56(44). 13776–13780. 43 indexed citations
8.
Newton, Christopher G., et al.. (2016). Masked Ketenes as Dienophiles in the Diels–Alder Reaction*. Australian Journal of Chemistry. 69(12). 1365–1374. 5 indexed citations
9.
Newton, Christopher G., et al.. (2015). [5]Radialene. Journal of the American Chemical Society. 137(46). 14653–14659. 27 indexed citations
10.
Newton, Christopher G., et al.. (2014). Pseudopterosin synthesis from a chiral cross-conjugated hydrocarbon through a series of cycloadditions. Nature Chemistry. 7(1). 82–86. 71 indexed citations
11.
Clark, David E. & Christopher G. Newton. (2004). Outsourcing lead optimisation – the quiet revolution. Drug Discovery Today. 9(11). 492–500. 20 indexed citations
12.
Newton, Christopher G.. (1996). Editorial Biologicals & Immunologicals: Patenting combinatorial libraries and associated technologies. Expert Opinion on Therapeutic Patents. 6(9). 827–835. 8 indexed citations
13.
Jones, Keith, et al.. (1996). Asymmetric induction ? to nitrogen in pyrrolidines and piperidines via radical chemistry. Journal of the Chemical Society Perkin Transactions 1. 1107–1107. 5 indexed citations
14.
Dean, P. M., et al.. (1995). New perspectives in drug design. Academic Press eBooks. 38 indexed citations
15.
Bridge, Andrew W., Michael B. Hursthouse, Christian W. Lehmann, David J. Lythgoe, & Christopher G. Newton. (1993). Novel cycloadditions of isoquinoline Reissert salts. Journal of the Chemical Society Perkin Transactions 1. 1839–1839. 10 indexed citations
16.
STEVENS, M. F. G., et al.. (1990). Antitumor imidazotetrazines. 20. Preparation of the 8-acid derivative of mitozolomide and its utility in the preparation of active antitumor agents. Journal of Medicinal Chemistry. 33(5). 1393–1399. 29 indexed citations
17.
18.
Newton, Christopher G., et al.. (1988). A novel approach to the 5a-aryldecahydro-2-benzazepine skeleton. Tetrahedron Letters. 29(31). 3841–3844. 4 indexed citations
20.
Newton, Christopher G., et al.. (1984). Cyclic meso-ionic compounds. Part 21. The examination of nitro-derivatives of meso-ionic heterocycles as potential pharmaceuticals. Journal of the Chemical Society Perkin Transactions 1. 63–63. 3 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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