Derek M. Dalton

829 total citations
17 papers, 693 citations indexed

About

Derek M. Dalton is a scholar working on Organic Chemistry, Molecular Biology and Process Chemistry and Technology. According to data from OpenAlex, Derek M. Dalton has authored 17 papers receiving a total of 693 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Organic Chemistry, 2 papers in Molecular Biology and 2 papers in Process Chemistry and Technology. Recurrent topics in Derek M. Dalton's work include Catalytic C–H Functionalization Methods (8 papers), Cyclopropane Reaction Mechanisms (7 papers) and Synthesis and Catalytic Reactions (4 papers). Derek M. Dalton is often cited by papers focused on Catalytic C–H Functionalization Methods (8 papers), Cyclopropane Reaction Mechanisms (7 papers) and Synthesis and Catalytic Reactions (4 papers). Derek M. Dalton collaborates with scholars based in United States. Derek M. Dalton's co-authors include Tomislav Rovis, Kevin M. Oberg, Daniel A. DiRocco, Todd K. Hyster, F. Dean Toste, Richard A. Mathies, Kenneth N. Raymond, Robert G. Bergman, Eva M. Nichols and Scott R. Ellis and has published in prestigious journals such as Journal of the American Chemical Society, Nature Chemistry and The Journal of Organic Chemistry.

In The Last Decade

Derek M. Dalton

16 papers receiving 687 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Derek M. Dalton United States 11 639 188 65 55 46 17 693
Kunbing Ouyang China 10 911 1.4× 181 1.0× 37 0.6× 43 0.8× 77 1.7× 20 973
М. А. Москаленко Russia 10 356 0.6× 227 1.2× 95 1.5× 41 0.7× 80 1.7× 30 468
Andrew P. Dominey United Kingdom 14 625 1.0× 251 1.3× 45 0.7× 65 1.2× 120 2.6× 23 708
Yusuke Kumatabara Japan 7 428 0.7× 168 0.9× 119 1.8× 28 0.5× 79 1.7× 7 528
Matthew V. Joannou United States 15 710 1.1× 251 1.3× 43 0.7× 38 0.7× 65 1.4× 24 781
Tomoyuki Yanagi Japan 15 780 1.2× 75 0.4× 49 0.8× 57 1.0× 44 1.0× 23 833
Wenju Chang China 14 622 1.0× 223 1.2× 132 2.0× 39 0.7× 51 1.1× 31 692

Countries citing papers authored by Derek M. Dalton

Since Specialization
Citations

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

Fields of papers citing papers by Derek M. Dalton

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Derek M. Dalton. 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 Derek M. Dalton. The network helps show where Derek M. Dalton may publish in the future.

Co-authorship network of co-authors of Derek M. Dalton

This figure shows the co-authorship network connecting the top 25 collaborators of Derek M. Dalton. A scholar is included among the top collaborators of Derek M. Dalton 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 Derek M. Dalton. Derek M. Dalton is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

17 of 17 papers shown
1.
Pompeo, Matthew, Sean M. Kelly, Derek M. Dalton, et al.. (2024). Umpolung Flow Chemistry for the Synthesis of a 3-Oxo-3H-spiro[benzofuran-2,4′-piperidine] Building Block. The Journal of Organic Chemistry. 89(11). 7618–7629. 1 indexed citations
2.
Dalton, Derek M., et al.. (2024). N1-Selective Methylation of Pyrazoles via α-Halomethylsilanes as Masked Methylating Reagents. The Journal of Organic Chemistry. 89(6). 4221–4224. 6 indexed citations
3.
Dalton, Derek M., et al.. (2024). Development of a Robust Pd-Catalyzed C–S Coupling for the Synthesis of Janus Kinase Inhibitor GDC-9918. Organic Process Research & Development. 28(10). 3858–3870.
4.
Dalton, Derek M., et al.. (2024). Utopia Point Bayesian Optimization Finds Condition-Dependent Selectivity for N-Methyl Pyrazole Condensation. Journal of the American Chemical Society. 146(23). 15779–15786. 7 indexed citations
5.
Sirois, Lauren E., et al.. (2024). Streamlined Synthesis of SHP2 Inhibitor GDC-1971 Enhanced by a Telescoped Schotten-Baumann SNAr and Reactive Crystallization Cascade. Organic Process Research & Development. 28(7). 2862–2874. 2 indexed citations
6.
Chu, John C. K., Derek M. Dalton, & Tomislav Rovis. (2015). Zn-Catalyzed Enantio- and Diastereoselective Formal [4 + 2] Cycloaddition Involving Two Electron-Deficient Partners: Asymmetric Synthesis of Piperidines from 1-Azadienes and Nitro-Alkenes. Journal of the American Chemical Society. 137(13). 4445–4452. 36 indexed citations
7.
8.
Dalton, Derek M., Scott R. Ellis, Eva M. Nichols, et al.. (2015). Supramolecular Ga4L612– Cage Photosensitizes 1,3-Rearrangement of Encapsulated Guest via Photoinduced Electron Transfer. Journal of the American Chemical Society. 137(32). 10128–10131. 100 indexed citations
9.
Hyster, Todd K., Derek M. Dalton, & Tomislav Rovis. (2014). Ligand design for Rh(iii)-catalyzed C–H activation: an unsymmetrical cyclopentadienyl group enables a regioselective synthesis of dihydroisoquinolones. Chemical Science. 6(1). 254–258. 130 indexed citations
10.
Rovis, Tomislav, et al.. (2013). SNAr-Derived Decomposition By-products Involving Pentafluorophenyl Triazolium Carbenes. Synlett. 24(10). 1229–1232. 13 indexed citations
11.
Dalton, Derek M., Anthony K. Rappé, & Tomislav Rovis. (2013). Perfluorinated Taddol phosphoramidite as an L,Z-ligand on Rh(i) and Co(−i): evidence for bidentate coordination via metal–C6F5 interaction. Chemical Science. 4(5). 2062–2062. 22 indexed citations
12.
Dalton, Derek M. & Tomislav Rovis. (2013). Catalytic, Asymmetric Indolizidinone Aza-Quaternary Stereocenter Synthesis: Expedient Synthesis of the Cylindricine Alkaloid Core. Organic Letters. 15(10). 2346–2349. 27 indexed citations
13.
Dalton, Derek M. & Tomislav Rovis. (2013). Catalytic, Asymmetric Indolizidinone Aza-Quaternary Stereocenter Synthesis: Expedient Synthesis of the Cylindricine Alkaloids Core. Organic Letters. 15(18). 4915–4915. 2 indexed citations
14.
Dalton, Derek M. & Tomislav Rovis. (2010). C–H carboxylation takes gold. Nature Chemistry. 2(9). 710–711. 60 indexed citations
15.
Oberg, Kevin M., et al.. (2010). Phosphoramidite-rhodium complexes as catalysts for the asymmetric [2 + 2 + 2] cycloaddition of alkenyl isocyanates and alkynes. Pure and Applied Chemistry. 82(7). 1353–1364. 27 indexed citations
16.
Dalton, Derek M., Kevin M. Oberg, Robert T. Yu, et al.. (2009). Enantioselective Rhodium-Catalyzed [2 + 2 + 2] Cycloadditions of Terminal Alkynes and Alkenyl Isocyanates: Mechanistic Insights Lead to a Unified Model that Rationalizes Product Selectivity. Journal of the American Chemical Society. 131(43). 15717–15728. 59 indexed citations
17.
DiRocco, Daniel A., Kevin M. Oberg, Derek M. Dalton, & Tomislav Rovis. (2009). Catalytic Asymmetric Intermolecular Stetter Reaction of Heterocyclic Aldehydes with Nitroalkenes: Backbone Fluorination Improves Selectivity. Journal of the American Chemical Society. 131(31). 10872–10874. 191 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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