D. Matthew Peacock

492 total citations
10 papers, 348 citations indexed

About

D. Matthew Peacock is a scholar working on Molecular Biology, Organic Chemistry and Inorganic Chemistry. According to data from OpenAlex, D. Matthew Peacock has authored 10 papers receiving a total of 348 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 5 papers in Organic Chemistry and 4 papers in Inorganic Chemistry. Recurrent topics in D. Matthew Peacock's work include Protein Kinase Regulation and GTPase Signaling (5 papers), Asymmetric Hydrogenation and Catalysis (4 papers) and Catalytic Cross-Coupling Reactions (3 papers). D. Matthew Peacock is often cited by papers focused on Protein Kinase Regulation and GTPase Signaling (5 papers), Asymmetric Hydrogenation and Catalysis (4 papers) and Catalytic Cross-Coupling Reactions (3 papers). D. Matthew Peacock collaborates with scholars based in United States, Japan and Canada. D. Matthew Peacock's co-authors include John F. Hartwig, Casey B. Roos, Kevan M. Shokat, Ziyang Zhang, Qinheng Zheng, Quan Jiang, Rong Gao, Hiroaki Suga, Qi Hu and Thomas R. Cundari and has published in prestigious journals such as Cell, Journal of the American Chemical Society and Cancer Research.

In The Last Decade

D. Matthew Peacock

9 papers receiving 339 citations

Peers

D. Matthew Peacock
Gail L. Wrigley United Kingdom
Stuart E. Pearson United Kingdom
Aaron Kunzer United States
Mark Charles United Kingdom
Susan L. Hockerman United States
Philip N. Collier United Kingdom
John L. Gilmore United States
Mihir D. Parikh United States
Gary Fairley United Kingdom
Alan Futran United States
Gail L. Wrigley United Kingdom
D. Matthew Peacock
Citations per year, relative to D. Matthew Peacock D. Matthew Peacock (= 1×) peers Gail L. Wrigley

Countries citing papers authored by D. Matthew Peacock

Since Specialization
Citations

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

Fields of papers citing papers by D. Matthew Peacock

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by D. Matthew Peacock. 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 D. Matthew Peacock. The network helps show where D. Matthew Peacock may publish in the future.

Co-authorship network of co-authors of D. Matthew Peacock

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

All Works

10 of 10 papers shown
1.
Morstein, Johannes, Vickie Bowcut, Yue Yang, et al.. (2024). Targeting Ras-, Rho-, and Rab-family GTPases via a conserved cryptic pocket. Cell. 187(22). 6379–6392.e17. 13 indexed citations
2.
Morstein, Johannes, et al.. (2024). Abstract B102: Development of covalent inhibitors targeting Ras Q61 hotspot mutants. Cancer Research. 84(2_Supplement). B102–B102.
3.
Peacock, D. Matthew, Mark J. S. Kelly, & Kevan M. Shokat. (2022). Probing the KRas Switch II Groove by Fluorine NMR Spectroscopy. ACS Chemical Biology. 17(10). 2710–2715. 6 indexed citations
4.
Vasta, James D., D. Matthew Peacock, Qinheng Zheng, et al.. (2022). KRAS is vulnerable to reversible switch-II pocket engagement in cells. Nature Chemical Biology. 18(6). 596–604. 72 indexed citations
5.
Zheng, Qinheng, D. Matthew Peacock, & Kevan M. Shokat. (2022). Drugging the Next Undruggable KRAS Allele-Gly12Asp. Journal of Medicinal Chemistry. 65(4). 3119–3122. 23 indexed citations
6.
Zhang, Ziyang, Rong Gao, Qi Hu, et al.. (2020). GTP-State-Selective Cyclic Peptide Ligands of K-Ras(G12D) Block Its Interaction with Raf. ACS Central Science. 6(10). 1753–1761. 77 indexed citations
7.
Peacock, D. Matthew, Quan Jiang, Patrick S. Hanley, Thomas R. Cundari, & John F. Hartwig. (2018). Reductive Elimination from Phosphine-Ligated Alkylpalladium(II) Amido Complexes To Form sp3 Carbon–Nitrogen Bonds. Journal of the American Chemical Society. 140(14). 4893–4904. 28 indexed citations
8.
Peacock, D. Matthew, Quan Jiang, Thomas R. Cundari, & John F. Hartwig. (2018). Reductive Elimination to Form C(sp3)–N Bonds from Palladium(II) Primary Alkyl Complexes. Organometallics. 37(19). 3243–3247. 14 indexed citations
9.
Jiang, Quan, D. Matthew Peacock, John F. Hartwig, & Thomas R. Cundari. (2018). Carbon(sp3)-nitrogen bond-forming reductive elimination from phosphine-ligated alkylpalladium(II) amide complexes: A DFT study. Tetrahedron. 75(2). 137–143. 3 indexed citations
10.
Peacock, D. Matthew, Casey B. Roos, & John F. Hartwig. (2016). Palladium-Catalyzed Cross Coupling of Secondary and Tertiary Alkyl Bromides with a Nitrogen Nucleophile. ACS Central Science. 2(9). 647–652. 112 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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