Timothy T. Curran

953 total citations
40 papers, 772 citations indexed

About

Timothy T. Curran is a scholar working on Organic Chemistry, Molecular Biology and Pharmaceutical Science. According to data from OpenAlex, Timothy T. Curran has authored 40 papers receiving a total of 772 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Organic Chemistry, 13 papers in Molecular Biology and 5 papers in Pharmaceutical Science. Recurrent topics in Timothy T. Curran's work include Synthetic Organic Chemistry Methods (10 papers), Asymmetric Synthesis and Catalysis (9 papers) and Chemical Synthesis and Analysis (6 papers). Timothy T. Curran is often cited by papers focused on Synthetic Organic Chemistry Methods (10 papers), Asymmetric Synthesis and Catalysis (9 papers) and Chemical Synthesis and Analysis (6 papers). Timothy T. Curran collaborates with scholars based in United States, United Kingdom and Poland. Timothy T. Curran's co-authors include Dale L. Boger, Annette M. Kasper, Wendy L. Corbett, David Hay, Koushik Das Sarma, Ji Zhang, Jonathan Evans, Ji Zhang, Mohammad Behforouz and Ian W. Ashworth and has published in prestigious journals such as Journal of the American Chemical Society, The Journal of Organic Chemistry and Tetrahedron.

In The Last Decade

Timothy T. Curran

39 papers receiving 735 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Timothy T. Curran United States 16 617 225 90 57 53 40 772
Michael C. Hillier United States 14 409 0.7× 199 0.9× 53 0.6× 19 0.3× 39 0.7× 21 521
Cristiano Raminelli Brazil 13 596 1.0× 155 0.7× 62 0.7× 36 0.6× 27 0.5× 59 780
Donald R. Gauthier United States 20 760 1.2× 249 1.1× 182 2.0× 125 2.2× 70 1.3× 37 1.0k
Josephine W. Reed United States 11 709 1.1× 289 1.3× 97 1.1× 28 0.5× 115 2.2× 15 916
Boguslaw Mudryk United States 17 553 0.9× 133 0.6× 67 0.7× 44 0.8× 17 0.3× 35 669
Christopher C. Nawrat United Kingdom 14 662 1.1× 171 0.8× 52 0.6× 57 1.0× 78 1.5× 26 821
Olivier Piva France 21 1.2k 2.0× 311 1.4× 152 1.7× 129 2.3× 72 1.4× 94 1.3k
Darren L. Reid United States 12 213 0.3× 157 0.7× 45 0.5× 51 0.9× 26 0.5× 27 514
Serge R. Piettre France 28 1.5k 2.4× 339 1.5× 146 1.6× 278 4.9× 90 1.7× 62 1.7k
John Limanto United States 15 560 0.9× 318 1.4× 192 2.1× 46 0.8× 36 0.7× 24 834

Countries citing papers authored by Timothy T. Curran

Since Specialization
Citations

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

Fields of papers citing papers by Timothy T. Curran

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Timothy T. Curran

This figure shows the co-authorship network connecting the top 25 collaborators of Timothy T. Curran. A scholar is included among the top collaborators of Timothy T. Curran 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 T. Curran. Timothy T. Curran 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.
Curran, Timothy T., et al.. (2024). On the role of digital tools in nitrosamine risk assessment for drug substance and drug product manufacturing processes. Current Opinion in Chemical Engineering. 45. 101030–101030. 2 indexed citations
2.
Ashworth, Ian W., Timothy T. Curran, Olivier Dirat, et al.. (2023). A Consideration of the Extent That Tertiary Amines Can Form N-Nitroso Dialkylamines in Pharmaceutical Products. Organic Process Research & Development. 27(10). 1714–1718. 18 indexed citations
3.
Ashworth, Ian W., Timothy T. Curran, J. Gair Ford, & Simone Tomasi. (2021). Prediction of N-Nitrosamine Partition Coefficients for Derisking Drug Substance Manufacturing Processes. Organic Process Research & Development. 25(4). 871–883. 15 indexed citations
4.
Borman, Phil J., Kevin D. Seibert, Sushil Srivastava, et al.. (2018). The Delivery of Flexibility from the Application of QbD to API Development. Journal of Pharmaceutical Innovation. 13(4). 367–372. 4 indexed citations
5.
Littler, Benjamin J., Michael Aizenberg, Narendra B. Ambhaikar, et al.. (2014). Development of a Manufacturing Process for an HCV Protease Inhibitor Candidate Molecule. Organic Process Research & Development. 19(1). 270–283. 8 indexed citations
6.
Lall, Manjinder S., Garrett Hoge, Tuan P. Tran, et al.. (2012). Stereoselective Synthesis of (S)-3-(Methylamino)-3-((R)-pyrrolidin-3-yl)propanenitrile. The Journal of Organic Chemistry. 77(10). 4732–4739. 17 indexed citations
7.
Bolton, Gary L., Timothy T. Curran, R. H. Hutchings, et al.. (2008). Preparation of a HMG-CoA Reductase Inhibitor via an Optimized Imidazole-Forming Condensation Reaction. Organic Process Research & Development. 12(6). 1183–1187. 5 indexed citations
8.
Curran, Timothy T.. (2008). ChemInform Abstract: Baeyer—Villiger Oxidation. ChemInform. 39(37). 1 indexed citations
9.
10.
Zhang, Ji, Koushik Das Sarma, & Timothy T. Curran. (2005). Efficient formation of novel and versatile building blocks from mucohalic acids: new substitute for tetronic acid and γ-alkylidenebutenolide. Tetrahedron Letters. 46(38). 6433–6436. 3 indexed citations
11.
Curran, Timothy T., et al.. (2005). A Simple, High Yield Route to cis-4-(N-Alkylamino)-L-Prolines. Letters in Organic Chemistry. 2(1). 15–17. 1 indexed citations
12.
Cregge, Robert J., Timothy T. Curran, & William A. Metz. (1998). A convenient synthesis of peptidyl perfluoroalkyl ketones. Journal of Fluorine Chemistry. 88(1). 71–77. 6 indexed citations
13.
Curran, Timothy T., et al.. (1997). The preparation of optically active 2-cyclopenten-1,4-diol derivatives from furfuryl alcohol. Tetrahedron. 53(6). 1983–2004. 71 indexed citations
14.
15.
Curran, Timothy T.. (1995). Implementation of the Dakin-West reaction for the preparation of an α-amino-pentafluoroethyl ketone. Journal of Fluorine Chemistry. 74(1). 107–112. 10 indexed citations
16.
Curran, Timothy T.. (1993). Preparation of .alpha.,.alpha.-difluoro-.beta.-hydroxy esters via a modified Reformatsky reaction. The Journal of Organic Chemistry. 58(23). 6360–6363. 28 indexed citations
17.
18.
Boger, Dale L., Wendy L. Corbett, Timothy T. Curran, & Annette M. Kasper. (1991). Inverse electron-demand Diels-Alder reactions of N-sulfonyl .alpha.,.beta.-unsaturated imines: a general approach to implementation of the 4.pi. participation of 1-aza-1,3-butadienes in Diels-Alder reactions. Journal of the American Chemical Society. 113(5). 1713–1729. 168 indexed citations
19.
20.
Behforouz, Mohammad, et al.. (1986). Regiospecific addition of organocopper reagents to α, gb-unsaturated esters. Tetrahedron Letters. 27(27). 3107–3110. 21 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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