Timothy E. Hurst

884 total citations
23 papers, 722 citations indexed

About

Timothy E. Hurst is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, Timothy E. Hurst has authored 23 papers receiving a total of 722 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Organic Chemistry, 8 papers in Molecular Biology and 2 papers in Pharmacology. Recurrent topics in Timothy E. Hurst's work include Catalytic C–H Functionalization Methods (9 papers), Catalytic Cross-Coupling Reactions (6 papers) and Synthesis of heterocyclic compounds (3 papers). Timothy E. Hurst is often cited by papers focused on Catalytic C–H Functionalization Methods (9 papers), Catalytic Cross-Coupling Reactions (6 papers) and Synthesis of heterocyclic compounds (3 papers). Timothy E. Hurst collaborates with scholars based in United Kingdom, Canada and Austria. Timothy E. Hurst's co-authors include Victor Snieckus, Christopher J. Moody, Richard J. K. Taylor, Matthew O. Kitching, Timothy J. Miles, Matthew D. Fletcher, Adrian C. Whitwood, Christopher J. Davis, Eduard Hartmann and Andrei S. Batsanov and has published in prestigious journals such as Angewandte Chemie International Edition, ACS Catalysis and The FASEB Journal.

In The Last Decade

Timothy E. Hurst

23 papers receiving 700 citations

Peers

Timothy E. Hurst
Deborah Smith United States
Yeung United States
Michael B. Mitchell United Kingdom
Richard K. Bellingham United Kingdom
Charles L. Sims United States
Qian Liao China
J. S. MENDOZA United States
Emily C. Cherney United States
Youseung Kim South Korea
Lakhwinder Singh India
Deborah Smith United States
Timothy E. Hurst
Citations per year, relative to Timothy E. Hurst Timothy E. Hurst (= 1×) peers Deborah Smith

Countries citing papers authored by Timothy E. Hurst

Since Specialization
Citations

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

Fields of papers citing papers by Timothy E. Hurst

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Timothy E. Hurst. 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 Timothy E. Hurst. The network helps show where Timothy E. Hurst may publish in the future.

Co-authorship network of co-authors of Timothy E. Hurst

This figure shows the co-authorship network connecting the top 25 collaborators of Timothy E. Hurst. A scholar is included among the top collaborators of Timothy E. Hurst 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 Timothy E. Hurst. Timothy E. Hurst 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.
Patel, Jignesh J., et al.. (2020). Expedient Pd‐Catalyzed α‐Arylation towards Dibenzoxepinones: Pivotal Manske's Ketone for the Formal Synthesis of Cularine Alkaloids. European Journal of Organic Chemistry. 2020(30). 4693–4697. 5 indexed citations
2.
Hurst, Timothy E., et al.. (2019). A copper(II)-mediated radical cross-dehydrogenative coupling/sulfinic acid elimination approach to 2-quinolones. Tetrahedron. 75(49). 130711–130711. 3 indexed citations
3.
Hurst, Timothy E., et al.. (2019). Sodium Methyl Carbonate as an Effective C1 Synthon. Synthesis of Carboxylic Acids, Benzophenones, and Unsymmetrical Ketones. Organic Letters. 21(11). 3882–3885. 29 indexed citations
4.
Wu, Danchen, Asish Dasgupta, Kuang‐Hueih Chen, et al.. (2019). Identification of novel dynamin‐related protein 1 (Drp1) GTPase inhibitors: Therapeutic potential of Drpitor1 and Drpitor1a in cancer and cardiac ischemia‐reperfusion injury. The FASEB Journal. 34(1). 1447–1464. 88 indexed citations
5.
Kuatsjah, Eugene, Anson Chan, Timothy E. Hurst, et al.. (2018). Metal- and Serine-Dependent Meta-Cleavage Product Hydrolases Utilize Similar Nucleophile-Activation Strategies. ACS Catalysis. 8(12). 11622–11632. 7 indexed citations
6.
7.
Crowe, Adam M., Israël Casabon, Jie Liu, et al.. (2017). Catabolism of the Last Two Steroid Rings in Mycobacterium tuberculosis and Other Bacteria. mBio. 8(2). 65 indexed citations
8.
Hurst, Timothy E. & Richard J. K. Taylor. (2016). A Cu‐Catalysed Radical Cross‐Dehydrogenative Coupling Approach to Acridanes and Related Heterocycles. European Journal of Organic Chemistry. 2017(1). 203–207. 11 indexed citations
9.
Hurst, Timothy E., et al.. (2015). Substrate scope in the copper-mediated construction of bis-oxindoles via a double C–H/Ar–H coupling process. Tetrahedron. 71(39). 7124–7136. 13 indexed citations
10.
11.
Hurst, Timothy E., et al.. (2014). A Direct CH/ArH Coupling Approach to Oxindoles, Thio‐oxindoles, 3,4‐Dihydro‐1 H‐quinolin‐2‐ones, and 1,2,3,4‐Tetrahydroquinolines. Chemistry - A European Journal. 20(43). 14063–14073. 40 indexed citations
12.
Hurst, Timothy E., et al.. (2014). Copper-Mediated Construction of Spirocyclic Bis-oxindoles via a Double C–H, Ar–H Coupling Process. Organic Letters. 16(18). 4900–4903. 37 indexed citations
13.
Kitching, Matthew O., Timothy E. Hurst, & Victor Snieckus. (2012). Copper‐Catalyzed Cross‐Coupling Interrupted by an Opportunistic Smiles Rearrangement: An Efficient Domino Approach to Dibenzoxazepinones. Angewandte Chemie International Edition. 51(12). 2925–2929. 61 indexed citations
14.
Kitching, Matthew O., Timothy E. Hurst, & Victor Snieckus. (2012). Copper‐Catalyzed Cross‐Coupling Interrupted by an Opportunistic Smiles Rearrangement: An Efficient Domino Approach to Dibenzoxazepinones. Angewandte Chemie. 124(12). 2979–2983. 21 indexed citations
15.
Hurst, Timothy E., Todd K. Macklin, M. Becker, et al.. (2010). Iridium‐Catalyzed CH Activation versus Directed ortho Metalation: Complementary Borylation of Aromatics and Heteroaromatics. Chemistry - A European Journal. 16(27). 8155–8161. 99 indexed citations
16.
Hurst, Timothy E., Timothy J. Miles, & Christopher J. Moody. (2007). Intramolecular Diels–Alder reactions of α,β-unsaturated oxime ethers as 1-azadienes: synthesis of [c]-fused pyridines. Tetrahedron. 64(5). 874–882. 11 indexed citations
17.
Fletcher, Matthew D., Timothy E. Hurst, Timothy J. Miles, & Christopher J. Moody. (2006). Synthesis of highly-functionalised pyridines via hetero-Diels–Alder methodology: reaction of 3-siloxy-1-aza-1,3-butadienes with electron deficient acetylenes. Tetrahedron. 62(23). 5454–5463. 60 indexed citations
18.
Fletcher, Matthew D., Timothy E. Hurst, Timothy J. Miles, & Christopher J. Moody. (2006). Synthesis of Highly‐Functionalized Pyridines via hetero‐Diels—Alder Methodology: Reaction of 3‐Siloxy‐1‐aza‐1,3‐butadienes with Electron Deficient Acetylenes.. ChemInform. 37(39). 4 indexed citations
19.
Bedford, Robin B., Craig P. Butts, Timothy E. Hurst, & Pelle Lidström. (2004). The Suzuki Coupling of Aryl Chlorides under Microwave Heating. Advanced Synthesis & Catalysis. 346(13-15). 1627–1630. 29 indexed citations
20.
Hurst, Timothy E., et al.. (1997). Gender differences in mediation of severe occupational stress among correctional officers. American Journal of Criminal Justice. 22(1). 121–137. 70 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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