Michelle Tran‐Dubé

1.6k total citations
17 papers, 416 citations indexed

About

Michelle Tran‐Dubé is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, Michelle Tran‐Dubé has authored 17 papers receiving a total of 416 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Organic Chemistry, 2 papers in Inorganic Chemistry and 1 paper in Molecular Biology. Recurrent topics in Michelle Tran‐Dubé's work include Catalytic C–H Functionalization Methods (10 papers), Cyclopropane Reaction Mechanisms (8 papers) and Catalytic Cross-Coupling Reactions (6 papers). Michelle Tran‐Dubé is often cited by papers focused on Catalytic C–H Functionalization Methods (10 papers), Cyclopropane Reaction Mechanisms (8 papers) and Catalytic Cross-Coupling Reactions (6 papers). Michelle Tran‐Dubé collaborates with scholars based in United States, France and China. Michelle Tran‐Dubé's co-authors include Indrawan McAlpine, Steven M. Mennen, Scott J. Miller, Jarred T. Blank, Jason E. Imbriglio, Keary M. Engle, Fen Wang, Neal W. Sach, Ryan L. Patman and Shouliang Yang and has published in prestigious journals such as Angewandte Chemie International Edition, Nature Communications and Chemical Communications.

In The Last Decade

Michelle Tran‐Dubé

16 papers receiving 411 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michelle Tran‐Dubé United States 11 379 74 65 46 13 17 416
Guofeng Zhao China 13 383 1.0× 108 1.5× 57 0.9× 16 0.3× 3 0.2× 28 430
Fangnuo Zhao China 8 325 0.9× 96 1.3× 39 0.6× 9 0.2× 8 0.6× 11 354
Ernest E. Lee Canada 12 403 1.1× 89 1.2× 62 1.0× 27 0.6× 16 459
Franck Silva United Kingdom 6 386 1.0× 55 0.7× 54 0.8× 107 2.3× 8 426
Xing Gao China 14 635 1.7× 124 1.7× 92 1.4× 28 0.6× 1 0.1× 24 668
Lyman J. Feron United Kingdom 5 211 0.6× 114 1.5× 66 1.0× 13 0.3× 7 256
Christine M. M. Hendriks Germany 7 510 1.3× 25 0.3× 79 1.2× 50 1.1× 8 555
Chaosheng Luo United States 8 305 0.8× 104 1.4× 59 0.9× 116 2.5× 1 0.1× 10 364
Guolin Wu China 11 467 1.2× 70 0.9× 55 0.8× 17 0.4× 1 0.1× 20 521
Jorge Hernández‐Toribio Spain 7 378 1.0× 92 1.2× 105 1.6× 34 0.7× 7 391

Countries citing papers authored by Michelle Tran‐Dubé

Since Specialization
Citations

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

Fields of papers citing papers by Michelle Tran‐Dubé

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michelle Tran‐Dubé. 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 Michelle Tran‐Dubé. The network helps show where Michelle Tran‐Dubé may publish in the future.

Co-authorship network of co-authors of Michelle Tran‐Dubé

This figure shows the co-authorship network connecting the top 25 collaborators of Michelle Tran‐Dubé. A scholar is included among the top collaborators of Michelle Tran‐Dubé 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 Michelle Tran‐Dubé. Michelle Tran‐Dubé 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.
Li, Jian, Indrawan McAlpine, Sajiv K. Nair, et al.. (2025). Microwave-Assisted Synthesis of Heterocycles via Rhodium(III)-Catalyzed C–H Activation: Norbornadiene as an Acetylene Equivalent. Organic Letters. 27(3). 728–733. 1 indexed citations
2.
Nair, Sajiv K., Ryan L. Patman, Sylvie K. Sakata, et al.. (2024). Construction of Isoquinolone Scaffolds on DNA via Rhodium(III)-Catalyzed C–H Activation. Organic Letters. 26(16). 3338–3342. 7 indexed citations
3.
Wang, Fen, Michelle Tran‐Dubé, Haiwei Xu, et al.. (2024). A Disconnection for Rapid Access to Heterocyclic Benzylic Amines with Fully Substituted α-Carbons. The Journal of Organic Chemistry. 89(6). 3926–3930.
4.
Ni, Hui‐Qi, Phillippa Cooper, Shouliang Yang, et al.. (2022). Mapping Ambiphile Reactivity Trends in the Anti‐(Hetero)annulation of Non‐Conjugated Alkenes via PdII/PdIV Catalysis. Angewandte Chemie International Edition. 61(13). e202114346–e202114346. 17 indexed citations
5.
Ni, Hui‐Qi, Ilia Kevlishvili, Joyann S. Barber, et al.. (2020). Anti-selective [3+2] (Hetero)annulation of non-conjugated alkenes via directed nucleopalladation. Nature Communications. 11(1). 6432–6432. 52 indexed citations
6.
Barber, Joyann S., Michael R. Collins, Michelle Tran‐Dubé, et al.. (2020). Development of a Late-Stage Diversification Strategy for the 4- and 5-Positions of 4,5,6-Trisubstituted Indazoles. Organic Letters. 22(22). 9047–9052. 2 indexed citations
7.
Medina, Jose M., Taeho Kang, Huiling Shao, et al.. (2019). Cu-Catalyzed Hydroboration of Benzylidenecyclopropanes: Reaction Optimization, (Hetero)Aryl Scope, and Origins of Pathway Selectivity. ACS Catalysis. 9(12). 11130–11136. 30 indexed citations
8.
Barber, Joyann S., Michelle Tran‐Dubé, Fen Wang, et al.. (2019). Rhodium(III)-Catalyzed C–H Activation: Ligand-Controlled Regioselective Synthesis of 4-Methyl-Substituted Dihydroisoquinolones. Organic Letters. 21(14). 5689–5693. 31 indexed citations
9.
Derosa, Joseph, Miriam L. O’Duill, Matthew Holcomb, et al.. (2018). Copper-Catalyzed Chan–Lam Cyclopropylation of Phenols and Azaheterocycles. The Journal of Organic Chemistry. 83(7). 3417–3425. 29 indexed citations
10.
McAlpine, Indrawan, Michelle Tran‐Dubé, Fen Wang, et al.. (2015). Synthesis of Small 3-Fluoro- and 3,3-Difluoropyrrolidines Using Azomethine Ylide Chemistry. The Journal of Organic Chemistry. 80(14). 7266–7274. 50 indexed citations
11.
Bernier, Louise, Michael R. Collins, Indrawan McAlpine, et al.. (2015). Improved cyclization conditions to prepare 6-substituted pyrazolo[1,5- a ]pyridines and pyrazolo[1,5- a ]pyrazines using catalytic Ag(I) and Au(III) salts. Tetrahedron Letters. 56(42). 5757–5760. 4 indexed citations
12.
13.
Wang, Fen, et al.. (2013). A simple and convenient two-step, one-pot synthesis of hetero-imidazoles from nitroaminoaryls catalyzed by Ytterbium triflate. Tetrahedron Letters. 54(31). 4054–4057. 11 indexed citations
14.
Tran‐Dubé, Michelle, et al.. (2012). A two-step, one-pot procedure using acid chlorides and propargyl amines to form tri-substituted oxazoles via gold-catalyzed cyclization. Tetrahedron Letters. 54(3). 259–261. 12 indexed citations
15.
Sach, Neal W., Michelle Tran‐Dubé, Huichun Zhu, et al.. (2012). Synthesis of Aryl Ethers via a Sulfonyl Transfer Reaction. Organic Letters. 14(15). 3886–3889. 28 indexed citations
16.
Tran‐Dubé, Michelle, Neal W. Sach, Sacha Ninkovic, et al.. (2012). The Synthesis of 3-pyrazinyl-pyrazolo [1,5-a] pyridines from an enol ether. Tetrahedron Letters. 53(33). 4372–4375. 4 indexed citations
17.
Mennen, Steven M., Jarred T. Blank, Michelle Tran‐Dubé, Jason E. Imbriglio, & Scott J. Miller. (2004). A peptide-catalyzed asymmetric Stetter reaction. Chemical Communications. 195–197. 105 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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