Andrew L. Lawrence

1.6k total citations
45 papers, 1.2k citations indexed

About

Andrew L. Lawrence is a scholar working on Organic Chemistry, Biochemistry and Molecular Biology. According to data from OpenAlex, Andrew L. Lawrence has authored 45 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Organic Chemistry, 10 papers in Biochemistry and 8 papers in Molecular Biology. Recurrent topics in Andrew L. Lawrence's work include Asymmetric Synthesis and Catalysis (12 papers), Chemical synthesis and alkaloids (11 papers) and Traditional and Medicinal Uses of Annonaceae (10 papers). Andrew L. Lawrence is often cited by papers focused on Asymmetric Synthesis and Catalysis (12 papers), Chemical synthesis and alkaloids (11 papers) and Traditional and Medicinal Uses of Annonaceae (10 papers). Andrew L. Lawrence collaborates with scholars based in United Kingdom, Australia and United States. Andrew L. Lawrence's co-authors include Michael S. Sherburn, Paul J. Lusby, Vicente Martí‐Centelles, Anthony C. Willis, Nicholas J. Green, Gary S. Nichol, Michael N. Paddon‐Row, Robert M. Adlington, Jack E. Baldwin and Amber L. Thompson and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Nature Chemistry.

In The Last Decade

Andrew L. Lawrence

45 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andrew L. Lawrence United Kingdom 21 896 240 158 143 121 45 1.2k
Ramón J. Zaragozá Spain 20 950 1.1× 289 1.2× 113 0.7× 191 1.3× 77 0.6× 82 1.3k
Manuel Arnó Spain 26 1.4k 1.6× 282 1.2× 103 0.7× 192 1.3× 69 0.6× 80 1.8k
Françoise Dumas France 21 980 1.1× 419 1.7× 110 0.7× 113 0.8× 46 0.4× 74 1.5k
Martha S. Morales‐Ríos Mexico 18 788 0.9× 196 0.8× 94 0.6× 74 0.5× 144 1.2× 98 1.1k
Razvan Simionescu Canada 17 545 0.6× 311 1.3× 146 0.9× 39 0.3× 181 1.5× 32 961
L. Straver France 10 375 0.4× 285 1.2× 130 0.8× 72 0.5× 67 0.6× 17 909
Ralph Kluge Germany 22 635 0.7× 483 2.0× 113 0.7× 47 0.3× 153 1.3× 82 1.3k
Philip J. Parsons United Kingdom 23 2.0k 2.2× 415 1.7× 189 1.2× 126 0.9× 144 1.2× 147 2.3k
M.L. Rodríguez Spain 19 636 0.7× 317 1.3× 77 0.5× 128 0.9× 56 0.5× 66 1.2k
Patrick H. Willoughby United States 14 933 1.0× 278 1.2× 84 0.5× 53 0.4× 35 0.3× 22 1.3k

Countries citing papers authored by Andrew L. Lawrence

Since Specialization
Citations

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

Fields of papers citing papers by Andrew L. Lawrence

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andrew L. Lawrence. 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 Andrew L. Lawrence. The network helps show where Andrew L. Lawrence may publish in the future.

Co-authorship network of co-authors of Andrew L. Lawrence

This figure shows the co-authorship network connecting the top 25 collaborators of Andrew L. Lawrence. A scholar is included among the top collaborators of Andrew L. Lawrence 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 Andrew L. Lawrence. Andrew L. Lawrence 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.
Richard, F., et al.. (2025). Quinol–Enedione Rearrangement. Organic Letters. 27(18). 4782–4787. 5 indexed citations
2.
Jones, David J., et al.. (2024). Stereoretentive enantioconvergent reactions. Nature Chemistry. 16(7). 1177–1183. 5 indexed citations
3.
Huang, David M., et al.. (2022). A bioinspired, one-step total synthesis of peshawaraquinone. Chemical Science. 14(4). 950–954. 5 indexed citations
4.
Trauner, Dirk, et al.. (2022). Natural product anticipation through synthesis. Nature Reviews Chemistry. 6(3). 170–181. 56 indexed citations
5.
Campopiano, Dominic J., et al.. (2021). N -Phenylputrescine (NPP): a natural product inspired amine donor for biocatalysis. Green Chemistry. 24(5). 2010–2016. 12 indexed citations
6.
Green, Nicholas J., et al.. (2021). Unified total synthesis of the brevianamide alkaloids enabled by chemical investigations into their biosynthesis. Chemical Science. 13(5). 1313–1322. 20 indexed citations
7.
Green, Nicholas J., et al.. (2020). Total synthesis of brevianamide A. Nature Chemistry. 12(7). 615–619. 61 indexed citations
8.
Martí‐Centelles, Vicente, Andrew L. Lawrence, & Paul J. Lusby. (2018). High Activity and Efficient Turnover by a Simple, Self-Assembled “Artificial Diels–Alderase”. Journal of the American Chemical Society. 140(8). 2862–2868. 205 indexed citations
9.
Lawrence, Andrew L., et al.. (2017). The importance of asking “how and why?” in natural product structure elucidation. Natural Product Reports. 34(10). 1193–1202. 45 indexed citations
10.
Lawrence, Andrew L., et al.. (2015). Hybrid Timber Construction – combining material properties for energy efficiency and sustainability. Report. 105. 110–119. 3 indexed citations
11.
Nörret, Marck, et al.. (2015). A Domino Diels–Alder Approach toward the Tetracyclic Nicandrenone Framework. Organic Letters. 17(22). 5517–5519. 19 indexed citations
12.
Lawrence, Andrew L., et al.. (2015). Unified total synthesis of the natural products endiandric acid A, kingianic acid E, and kingianins A, D, and F. Chemical Science. 6(7). 3886–3890. 37 indexed citations
13.
Campbell, Alexander, et al.. (2014). Molecular Identification of Diaspididae and Elucidation of Non-Native Species Using the Genes 28s and 16s. Insects. 5(3). 528–538. 9 indexed citations
14.
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
15.
Paddon‐Row, Michael N., et al.. (2014). Total Synthesis of Ramonanins A–D. Angewandte Chemie. 127(6). 1815–1818. 2 indexed citations
16.
Paddon‐Row, Michael N., et al.. (2014). Total Synthesis of Ramonanins A–D. Angewandte Chemie International Edition. 54(6). 1795–1798. 17 indexed citations
17.
Green, Nicholas J., Andrew L. Lawrence, Gomotsang Bojase, et al.. (2013). Domino Cycloaddition Organocascades of Dendralenes. Angewandte Chemie. 125(32). 8491–8494. 20 indexed citations
18.
Lawrence, Andrew L., et al.. (2013). Total Synthesis of Kingianins A, D, and F. Angewandte Chemie International Edition. 52(15). 4221–4224. 64 indexed citations
19.
Willis, Anthony C., et al.. (2013). Total Synthesis and Structural Revision of the Alkaloid Incargranine B. Angewandte Chemie International Edition. 52(50). 13273–13275. 48 indexed citations
20.
Willis, Anthony C., et al.. (2012). Total Synthesis of Incarviditone and Incarvilleatone. Organic Letters. 14(17). 4537–4539. 58 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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