Michael Rubin

5.6k total citations · 1 hit paper
137 papers, 4.6k citations indexed

About

Michael Rubin is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, Michael Rubin has authored 137 papers receiving a total of 4.6k indexed citations (citations by other indexed papers that have themselves been cited), including 130 papers in Organic Chemistry, 15 papers in Molecular Biology and 10 papers in Inorganic Chemistry. Recurrent topics in Michael Rubin's work include Cyclopropane Reaction Mechanisms (54 papers), Catalytic C–H Functionalization Methods (31 papers) and Catalytic Alkyne Reactions (25 papers). Michael Rubin is often cited by papers focused on Cyclopropane Reaction Mechanisms (54 papers), Catalytic C–H Functionalization Methods (31 papers) and Catalytic Alkyne Reactions (25 papers). Michael Rubin collaborates with scholars based in United States, Russia and Japan. Michael Rubin's co-authors include Vladimir Gevorgyan, Marina Rubina, Yoshinori Yamamoto, Todd Schwier, William M. Sherrill, А. В. Аксенов, Nicolai A. Aksenov, Дмитрий А. Аксенов, Andrew Edwards and Jianxiu Liu and has published in prestigious journals such as Chemical Reviews, Journal of the American Chemical Society and SHILAP Revista de lepidopterología.

In The Last Decade

Michael Rubin

136 papers receiving 4.6k citations

Hit Papers

Transition Metal Chemistry of Cyclopropenes and Cycloprop... 2007 2026 2013 2019 2007 250 500 750 1000

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michael Rubin United States 30 4.4k 808 547 173 134 137 4.6k
Tomoya Miura Japan 47 6.4k 1.4× 1.1k 1.3× 645 1.2× 295 1.7× 152 1.1× 160 6.7k
Jonathan T. Reeves United States 33 3.1k 0.7× 872 1.1× 788 1.4× 283 1.6× 154 1.1× 84 3.5k
Zhenghu Xu China 40 3.9k 0.9× 589 0.7× 513 0.9× 265 1.5× 165 1.2× 109 4.3k
Bertrand Carboni France 32 3.3k 0.8× 440 0.5× 1.0k 1.9× 122 0.7× 231 1.7× 165 3.7k
Jean-François Marcoux United States 22 4.5k 1.0× 695 0.9× 597 1.1× 230 1.3× 266 2.0× 35 4.9k
H. Lebel Canada 34 4.7k 1.1× 908 1.1× 444 0.8× 211 1.2× 94 0.7× 91 5.0k
Davide Audisio France 32 2.0k 0.5× 373 0.5× 785 1.4× 373 2.2× 142 1.1× 93 2.7k
Masamichi Ogasawara Japan 41 5.5k 1.2× 2.6k 3.2× 728 1.3× 166 1.0× 132 1.0× 142 5.8k
Steven T. Diver United States 28 3.5k 0.8× 539 0.7× 1.3k 2.4× 54 0.3× 138 1.0× 75 3.9k
Renhua Fan China 30 2.9k 0.6× 314 0.4× 410 0.7× 105 0.6× 96 0.7× 101 3.1k

Countries citing papers authored by Michael Rubin

Since Specialization
Citations

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

Fields of papers citing papers by Michael Rubin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michael Rubin. 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 Michael Rubin. The network helps show where Michael Rubin may publish in the future.

Co-authorship network of co-authors of Michael Rubin

This figure shows the co-authorship network connecting the top 25 collaborators of Michael Rubin. A scholar is included among the top collaborators of Michael Rubin 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 Michael Rubin. Michael Rubin 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.
Aksenov, Nicolai A., А. В. Аксенов, И. В. Аксенова, et al.. (2023). Synthesis of β-Carbolines with Electrocyclic Cyclization of 3-Nitrovinylindoles. International Journal of Molecular Sciences. 24(17). 13107–13107. 3 indexed citations
2.
Аксенов, Дмитрий А., et al.. (2022). Improved Method for Preparation of 3-(1H-Indol-3-yl)benzofuran-2(3H)-ones. Molecules. 27(6). 1902–1902. 3 indexed citations
3.
Аксенов, А. В., et al.. (2021). Electrophilically Activated Nitroalkanes in Synthesis of 3,4-Dihydroquinozalines. Molecules. 26(14). 4274–4274. 5 indexed citations
4.
Аксенов, А. В., et al.. (2021). Direct Conversion of 3-(2-Nitroethyl)-1H-Indoles into 2-(1H-Indol-2-yl)Acetonitriles. Molecules. 26(20). 6132–6132. 7 indexed citations
5.
Аксенов, А. В., Дмитрий А. Аксенов, Nicolai A. Aksenov, et al.. (2021). [3 + 2]-Annulation of pyridinium ylides with 1-chloro-2-nitrostyrenes unveils a tubulin polymerization inhibitor. Organic & Biomolecular Chemistry. 19(33). 7234–7245. 20 indexed citations
6.
Аксенов, Дмитрий А., et al.. (2020). Synthesis of imidazo[1,5-a]pyridines via cyclocondensation of 2-(aminomethyl)pyridines with electrophilically activated nitroalkanes. Beilstein Journal of Organic Chemistry. 16. 2903–2910. 7 indexed citations
8.
Аксенов, А. В., et al.. (2018). Unexpected cyclization of 2-(2-aminophenyl)indoles with nitroalkenes to furnish indolo[3,2-c]quinolines. Organic & Biomolecular Chemistry. 16(23). 4325–4332. 18 indexed citations
9.
Edwards, Andrew, Marina Rubina, & Michael Rubin. (2017). Directed RhI‐Catalyzed Asymmetric Hydroboration of Prochiral 1‐Arylcycloprop‐2‐Ene‐1‐Carboxylic Acid Derivatives. Chemistry - A European Journal. 24(6). 1394–1403. 45 indexed citations
10.
Dubovtsev, Alexey Yu., М. В. Дмитриев, А. Н. Масливец, & Michael Rubin. (2017). Regiodivergent condensation of 5-alkoxycarbonyl-1H-pyrrol-2,3-diones with cyclic ketazinones en route to spirocyclic scaffolds. Beilstein Journal of Organic Chemistry. 13. 2179–2185. 2 indexed citations
11.
Аксенов, А. В., Дмитрий А. Аксенов, Nicolai A. Aksenov, et al.. (2017). One-Pot, Three-Component Assembly of Indoloquinolines: Total Synthesis of Isocryptolepine. The Journal of Organic Chemistry. 82(6). 3011–3018. 26 indexed citations
12.
Аксенов, А. В., et al.. (2014). Highly efficient modular metal-free synthesis of 3-substituted 2-quinolones. Organic & Biomolecular Chemistry. 12(48). 9786–9788. 22 indexed citations
13.
Аксенов, А. В., А. Н. Смирнов, Nicolai A. Aksenov, et al.. (2013). Metal-free transannulation reaction of indoles with nitrostyrenes: a simple practical synthesis of 3-substituted 2-quinolones. Chemical Communications. 49(81). 9305–9305. 40 indexed citations
14.
Lewis, Frederick D., et al.. (2006). Solvent dependent photocyclization and photophysics of some 2-ethynylbiphenyls. Photochemical & Photobiological Sciences. 5(4). 369–375. 9 indexed citations
15.
Gevorgyan, Vladimir, Michael Rubin, & Marina Rubina. (2006). Recent Advances in Cyclopropene Chemistry. Synthesis. 2006(8). 1221–1245. 35 indexed citations
16.
Lewis, Frederick D., et al.. (2005). Ring-Closing Photoisomerization of Some 2,6-Diarylstyrenes†. Photochemistry and Photobiology. 82(1). 119–119. 3 indexed citations
17.
Chuprakov, Stepan, Michael Rubin, & Vladimir Gevorgyan. (2005). Direct Palladium-Catalyzed Arylation of Cyclopropenes. Journal of the American Chemical Society. 127(11). 3714–3715. 54 indexed citations
18.
Rubin, Michael, et al.. (1998). Diastereoselective palladium(0)-catalyzed azidation of 1-alkenylcyclopropyl esters: asymmetric synthesis of (−)-(1R,2S)-norcoronamic acid. Tetrahedron Asymmetry. 9(7). 1131–1135. 26 indexed citations
20.
Mokyr, Margalit B., et al.. (1993). Involvement of TCR-V beta 8.3+ cells in the cure of mice bearing a large MOPC-315 tumor by low dose melphalan.. The Journal of Immunology. 151(9). 4838–4846. 17 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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