David C. Moebius

750 total citations
12 papers, 648 citations indexed

About

David C. Moebius is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, David C. Moebius has authored 12 papers receiving a total of 648 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Organic Chemistry, 5 papers in Molecular Biology and 2 papers in Pharmacology. Recurrent topics in David C. Moebius's work include Cyclopropane Reaction Mechanisms (6 papers), Asymmetric Synthesis and Catalysis (5 papers) and Synthetic Organic Chemistry Methods (4 papers). David C. Moebius is often cited by papers focused on Cyclopropane Reaction Mechanisms (6 papers), Asymmetric Synthesis and Catalysis (5 papers) and Synthetic Organic Chemistry Methods (4 papers). David C. Moebius collaborates with scholars based in United States. David C. Moebius's co-authors include Jason S. Kingsbury, Brian A. Sparling, Matthew D. Shair, Andrew J. Wommack, Amir H. Hoveyda, Richard R. Schrock, Elizabeth S. Sattely, Tony Muchamuel, Jennifer A. Dabrowski and Dustin L. McMinn and has published in prestigious journals such as Journal of the American Chemical Society, Journal of Medicinal Chemistry and Organic Letters.

In The Last Decade

David C. Moebius

11 papers receiving 641 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David C. Moebius United States 10 464 176 92 68 58 12 648
Jung‐Nyoung Heo South Korea 18 653 1.4× 256 1.5× 26 0.3× 62 0.9× 50 0.9× 41 874
Taradas Sarkar United States 14 431 0.9× 206 1.2× 25 0.3× 76 1.1× 27 0.5× 21 626
Emmanuel Bertounesque France 17 511 1.1× 333 1.9× 31 0.3× 53 0.8× 47 0.8× 37 725
Darin J. Gustin United States 15 253 0.5× 267 1.5× 27 0.3× 133 2.0× 20 0.3× 20 548
Shende Jiang China 15 430 0.9× 265 1.5× 18 0.2× 72 1.1× 39 0.7× 50 617
Marı́a Ruiz Spain 17 408 0.9× 254 1.4× 31 0.3× 29 0.4× 59 1.0× 41 549
Bainian Feng China 14 282 0.6× 181 1.0× 28 0.3× 19 0.3× 28 0.5× 38 477
Akihiro Ogura Japan 14 424 0.9× 337 1.9× 22 0.2× 24 0.4× 20 0.3× 41 631
Mateusz Daśko Poland 12 406 0.9× 206 1.2× 15 0.2× 54 0.8× 54 0.9× 30 630
Joseph Sandoval United States 13 268 0.6× 132 0.8× 17 0.2× 77 1.1× 19 0.3× 17 404

Countries citing papers authored by David C. Moebius

Since Specialization
Citations

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

Fields of papers citing papers by David C. Moebius

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David C. Moebius. 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 David C. Moebius. The network helps show where David C. Moebius may publish in the future.

Co-authorship network of co-authors of David C. Moebius

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

All Works

12 of 12 papers shown
2.
Johnson, Henry W. B., Janet L. Anderl, Erin K. Bradley, et al.. (2017). Discovery of Highly Selective Inhibitors of the Immunoproteasome Low Molecular Mass Polypeptide 2 (LMP2) Subunit. ACS Medicinal Chemistry Letters. 8(4). 413–417. 32 indexed citations
3.
Sparling, Brian A., et al.. (2015). Total Synthesis of (−)-Nemorosone and (+)-Secohyperforin. Organic Letters. 17(14). 3398–3401. 36 indexed citations
4.
Moebius, David C., et al.. (2014). Catalysis of Diazoalkane–Carbonyl Homologation. How New Developments in Hydrazone Oxidation Enable the Carbon Insertion Strategy for Synthesis. Topics in current chemistry. 111–162. 36 indexed citations
5.
Sparling, Brian A., David C. Moebius, & Matthew D. Shair. (2012). Enantioselective Total Synthesis of Hyperforin. Journal of the American Chemical Society. 135(2). 644–647. 104 indexed citations
6.
Moebius, David C., et al.. (2011). An Enantioselective Synthesis of 2-Aryl Cycloalkanones by Sc-Catalyzed Carbon Insertion. Organic Letters. 13(8). 2004–2007. 84 indexed citations
8.
Moebius, David C. & Jason S. Kingsbury. (2009). Catalytic Homologation of Cycloalkanones with Substituted Diazomethanes. Mild and Efficient Single-Step Access to α-Tertiary and α-Quaternary Carbonyl Compounds. Journal of the American Chemical Society. 131(3). 878–879. 90 indexed citations
9.
Wommack, Andrew J., et al.. (2009). Sc(OTf)3-Catalyzed Carbon Insertion into FormylC-H Bond of Aldehydes. Synfacts. 2009(10). 1141–1141. 1 indexed citations
10.
Wommack, Andrew J., et al.. (2009). Diverse Alkanones by Catalytic Carbon Insertion into the Formyl C−H Bond. Concise Access to the Natural Precursor of Achyrofuran. Organic Letters. 11(15). 3202–3205. 53 indexed citations
11.
Sattely, Elizabeth S., et al.. (2005). Enantioselective Synthesis of Cyclic Amides and Amines through Mo-Catalyzed Asymmetric Ring-Closing Metathesis. Journal of the American Chemical Society. 127(23). 8526–8533. 77 indexed citations
12.
Sattely, Elizabeth S., et al.. (2005). Enantioselective Synthesis of Cyclic Amides and Amines Through Mo‐Catalyzed Asymmetric Ring‐Closing Metathesis.. ChemInform. 36(42). 1 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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