Lee T. Boulton

1.1k total citations · 1 hit paper
22 papers, 889 citations indexed

About

Lee T. Boulton is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, Lee T. Boulton has authored 22 papers receiving a total of 889 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Organic Chemistry, 9 papers in Molecular Biology and 7 papers in Inorganic Chemistry. Recurrent topics in Lee T. Boulton's work include Chemical Synthesis and Analysis (9 papers), Asymmetric Hydrogenation and Catalysis (7 papers) and Synthetic Organic Chemistry Methods (5 papers). Lee T. Boulton is often cited by papers focused on Chemical Synthesis and Analysis (9 papers), Asymmetric Hydrogenation and Catalysis (7 papers) and Synthetic Organic Chemistry Methods (5 papers). Lee T. Boulton collaborates with scholars based in United Kingdom, United States and Netherlands. Lee T. Boulton's co-authors include Marco T. Sabatini, Tom D. Sheppard, Helen F. Sneddon, David M. Hodgson, Graham N. Maw, Bernd Jandeleit, Michael Härter, K. C. Nicolaou, Rachel M. Lanigan and Ian C. Lennon and has published in prestigious journals such as Chemical Communications, Science Advances and Chemistry - A European Journal.

In The Last Decade

Lee T. Boulton

22 papers receiving 863 citations

Hit Papers

A green chemistry perspective on catalytic amide bond for... 2019 2026 2021 2023 2019 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lee T. Boulton United Kingdom 15 709 512 211 78 53 22 889
Gerald A. Weisenburger United States 12 1.1k 1.5× 545 1.1× 271 1.3× 93 1.2× 34 0.6× 24 1.2k
Marco T. Sabatini United Kingdom 9 546 0.8× 498 1.0× 151 0.7× 47 0.6× 46 0.9× 10 755
Michael J. Zacuto United States 18 856 1.2× 168 0.3× 151 0.7× 54 0.7× 24 0.5× 29 946
William S. Kissel United States 10 444 0.6× 210 0.4× 200 0.9× 62 0.8× 19 0.4× 13 580
Humberto Rodríguez‐Solla Spain 25 1.6k 2.3× 461 0.9× 326 1.5× 52 0.7× 37 0.7× 102 1.8k
Joseph P. A. Harrity United Kingdom 16 1.7k 2.4× 745 1.5× 206 1.0× 41 0.5× 28 0.5× 24 1.8k
Andrew D. Campbell United Kingdom 14 952 1.3× 266 0.5× 127 0.6× 61 0.8× 41 0.8× 27 1.2k
Klaus Langemann Germany 9 1.1k 1.6× 539 1.1× 109 0.5× 55 0.7× 53 1.0× 10 1.2k
Eric C. Hansen United States 19 1.2k 1.7× 303 0.6× 190 0.9× 93 1.2× 11 0.2× 31 1.3k
Zhongmin Xu United States 13 613 0.9× 241 0.5× 129 0.6× 28 0.4× 35 0.7× 22 714

Countries citing papers authored by Lee T. Boulton

Since Specialization
Citations

This map shows the geographic impact of Lee T. Boulton'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 Lee T. Boulton with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lee T. Boulton more than expected).

Fields of papers citing papers by Lee T. Boulton

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lee T. Boulton. 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 Lee T. Boulton. The network helps show where Lee T. Boulton may publish in the future.

Co-authorship network of co-authors of Lee T. Boulton

This figure shows the co-authorship network connecting the top 25 collaborators of Lee T. Boulton. A scholar is included among the top collaborators of Lee T. Boulton 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 Lee T. Boulton. Lee T. Boulton 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.
Murray, Ben J., Lee T. Boulton, Juan A. Aguilar, et al.. (2023). HFO‐1234yf as a CF 3 Building Block: Synthesis of Trifluoromethyl Quinoline and Chromene Derivatives from Trifluoromethyl‐ynones. European Journal of Organic Chemistry. 26(11). 4 indexed citations
2.
Pratley, Cassie, et al.. (2023). Development of a Horizontal Dynamically Mixed Flow Reactor for Laboratory Scale-Up of Photochemical Wohl–Ziegler Bromination. Organic Process Research & Development. 28(5). 1725–1733. 14 indexed citations
3.
Murray, Ben J., Lee T. Boulton, & Graham Sandford. (2021). HFO-1234yf as a CF3-building block: Synthesis of trifluoromethyl-benzophenone derivatives by deoxygenative aromatisation. Journal of Fluorine Chemistry. 245. 109774–109774. 3 indexed citations
4.
Murray, Ben J., Dmitri S. Yufit, Mark A. Fox, et al.. (2020). HFO‐1234yf as a CF3‐Building Block: Synthesis and Chemistry of CF3‐Ynones. European Journal of Organic Chemistry. 2020(39). 6236–6244. 19 indexed citations
5.
Boulton, Lee T., et al.. (2020). Ruthenium-Catalyzed Ester Reductions Applied to Pharmaceutical Intermediates. Organic Process Research & Development. 24(11). 2745–2751. 19 indexed citations
6.
Sabatini, Marco T., Lee T. Boulton, Helen F. Sneddon, & Tom D. Sheppard. (2019). A green chemistry perspective on catalytic amide bond formation. Nature Catalysis. 2(1). 10–17. 339 indexed citations breakdown →
7.
Sabatini, Marco T., et al.. (2018). Protecting‐Group‐Free Amidation of Amino Acids using Lewis Acid Catalysts. Chemistry - A European Journal. 24(27). 7033–7043. 47 indexed citations
8.
Sabatini, Marco T., Lee T. Boulton, & Tom D. Sheppard. (2017). Borate esters: Simple catalysts for the sustainable synthesis of complex amides. Science Advances. 3(9). e1701028–e1701028. 159 indexed citations
9.
Lanigan, Rachel M., et al.. (2016). Direct amidation of unprotected amino acids using B(OCH2CF3)3. Chemical Communications. 52(57). 8846–8849. 38 indexed citations
10.
Boulton, Lee T., et al.. (2012). The Large-Scale Synthesis of (S)-N-Boc-bis(4-fluorophenyl)alanine. Organic Process Research & Development. 17(1). 69–76. 21 indexed citations
11.
Boulton, Lee T., Christopher J. Cobley, Catherine Hill, et al.. (2005). Efficient Synthesis of an Imidazole-Substituted δ-Amino Acid by the Integration of Chiral Technologies. Organic Letters. 7(10). 1931–1934. 10 indexed citations
12.
Boulton, Lee T., Martin E. Fox, Paul B. Hodgson, & Ian C. Lennon. (2004). Zinc-mediated intramolecular acyl and imino transfer reactions of aryl iodides. Tetrahedron Letters. 46(6). 983–986. 5 indexed citations
13.
Boulton, Lee T., Ian C. Lennon, & Raymond McCague. (2003). Asymmetric hydrogenation of a 4,4-diaryl-3-butenoate; a novel approach to sertraline. Organic & Biomolecular Chemistry. 1(7). 1094–1096. 26 indexed citations
14.
Boulton, Lee T., Martin E. Fox, Mark Jackson, et al.. (2002). Synthesis of the Potent Antiglaucoma Agent, Travoprost. Organic Process Research & Development. 6(2). 138–145. 24 indexed citations
15.
Boulton, Lee T., et al.. (1999). Generation of unnatural α,α-disubstituted amino acid derivatives from cyclic sulfamidates. Journal of the Chemical Society Perkin Transactions 1. 1421–1430. 41 indexed citations
16.
17.
Nicolaou, K. C., Michael Härter, Lee T. Boulton, & Bernd Jandeleit. (1997). Synthesis of the Bicyclic Core of CP‐225,917 and CP‐263,114 by an Intramolecular Diels–Alder Reaction. Angewandte Chemie International Edition in English. 36(11). 1194–1196. 37 indexed citations
18.
Hodgson, David M., Lee T. Boulton, & Graham N. Maw. (1995). An Efficient Medium-Ring Cyclisation Approach to the Germacranes. Synlett. 1995(3). 267–268. 6 indexed citations
19.
Hodgson, David M., Lee T. Boulton, & Graham N. Maw. (1995). Scope of the chromium(II)-mediated synthesis of E-alkenylstannanes from aldehydes and Bu3SnCHBr2. Tetrahedron. 51(12). 3713–3724. 25 indexed citations
20.
Hodgson, David M., Lee T. Boulton, & Graham N. Maw. (1994). Chemoselectivity in the chromium(II)-mediated synthesis of E-alkenylstannanes from aldehydes and Bu3SnCHBr2. Tetrahedron Letters. 35(14). 2231–2234. 17 indexed citations

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