László Kürti

3.9k total citations
71 papers, 3.3k citations indexed

About

László Kürti is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, László Kürti has authored 71 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 65 papers in Organic Chemistry, 10 papers in Inorganic Chemistry and 9 papers in Molecular Biology. Recurrent topics in László Kürti's work include Catalytic C–H Functionalization Methods (25 papers), Synthesis and Catalytic Reactions (23 papers) and Asymmetric Synthesis and Catalysis (13 papers). László Kürti is often cited by papers focused on Catalytic C–H Functionalization Methods (25 papers), Synthesis and Catalytic Reactions (23 papers) and Asymmetric Synthesis and Catalysis (13 papers). László Kürti collaborates with scholars based in United States, China and Hungary. László Kürti's co-authors include Daniel H. Ess, Hongyin Gao, Muhammed Yousufuddin, Zhe Zhou, Zhiwei Ma, John R. Falck, Qing‐Long Xu, Craig Keene, E. J. Corey and Gongqiang Li and has published in prestigious journals such as Science, Journal of the American Chemical Society and Angewandte Chemie International Edition.

In The Last Decade

László Kürti

69 papers receiving 3.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
László Kürti United States 32 2.9k 497 474 467 210 71 3.3k
Françoise Colobert France 31 3.1k 1.0× 593 1.2× 506 1.1× 387 0.8× 200 1.0× 107 3.3k
Giorgio Bencivenni Italy 32 4.5k 1.5× 581 1.2× 624 1.3× 571 1.2× 193 0.9× 59 4.6k
Daniel R. Fandrick United States 24 2.4k 0.8× 486 1.0× 575 1.2× 477 1.0× 102 0.5× 48 2.7k
Dixit Parmar United Kingdom 11 2.7k 0.9× 413 0.8× 680 1.4× 331 0.7× 170 0.8× 15 2.9k
Vladimir B. Birman United States 32 3.1k 1.1× 311 0.6× 856 1.8× 944 2.0× 145 0.7× 55 3.4k
Jean Rodriguez France 34 3.8k 1.3× 980 2.0× 425 0.9× 691 1.5× 267 1.3× 108 3.9k
Xufeng Lin China 37 3.8k 1.3× 492 1.0× 567 1.2× 709 1.5× 218 1.0× 122 4.0k
Marco Bella Italy 34 4.1k 1.4× 504 1.0× 1.0k 2.1× 853 1.8× 194 0.9× 77 4.4k
Sadiya Raja Germany 13 2.8k 1.0× 420 0.8× 718 1.5× 352 0.8× 162 0.8× 15 3.0k
Aaron Aponick United States 30 2.6k 0.9× 164 0.3× 656 1.4× 464 1.0× 83 0.4× 74 3.0k

Countries citing papers authored by László Kürti

Since Specialization
Citations

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

Fields of papers citing papers by László Kürti

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of László Kürti

This figure shows the co-authorship network connecting the top 25 collaborators of László Kürti. A scholar is included among the top collaborators of László Kürti 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 László Kürti. László Kürti 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.
Mykhailiuk, Pavel K., et al.. (2025). Harnessing O -Vinylhydroxylamines for Ring-Annulation: A Scalable Approach to Azaindolines and Azaindoles. Journal of the American Chemical Society. 147(31). 27148–27154. 3 indexed citations
2.
Das, Tamal, et al.. (2024). Organocatalytic Electrophilic Arene Amination: Rapid Synthesis of 2‐Quinolones. Chemistry - A European Journal. 31(6). e202403524–e202403524. 2 indexed citations
3.
4.
Lin, Alex W. H., et al.. (2024). Oxidative Nitrogen Insertion into Silyl Enol Ether C═C Bonds. Journal of the American Chemical Society. 146(30). 21129–21136. 12 indexed citations
5.
Shah, Kush N., Parth N. Shah, Hongyin Gao, et al.. (2024). Antimicrobial activity of a natural compound and analogs against multi-drug-resistant Gram-positive pathogens. Microbiology Spectrum. 12(3). e0151522–e0151522. 6 indexed citations
6.
Elias, Welman C., Kimberly N. Heck, Bo Wang, et al.. (2023). Niobium Oxide Photocatalytically Oxidizes Ammonia in Water at Ambient Conditions. Journal of the Brazilian Chemical Society.
7.
Renard, David, Aaron Bayles, Benjamin D. Clark, et al.. (2022). Plasmon-Generated Solvated Electrons for Chemical Transformations. Journal of the American Chemical Society. 144(44). 20183–20189. 20 indexed citations
8.
Kattamuri, Padmanabha V., et al.. (2022). Aza-Quasi-Favorskii Reaction: Construction of Highly Substituted Aziridines through a Concerted Multibond Rearrangement Process. Journal of the American Chemical Society. 144(24). 10943–10949. 7 indexed citations
9.
Kürti, László, et al.. (2020). Synthesis of Highly Substituted Cyclopropanes via the Quasi-Favorskii Rearrangement of α,α-Dichlorocyclobutanols. Organic Letters. 22(15). 5715–5720. 8 indexed citations
10.
Kattamuri, Padmanabha V., et al.. (2020). Arylboronic Acid-Catalyzed C -Allylation of Unprotected Oximes: Total Synthesis of N -Me-Euphococcine. Organic Letters. 22(6). 2486–2489. 9 indexed citations
11.
Yousufuddin, Muhammed, et al.. (2020). Total synthesis of isatindigotindoline C. Organic & Biomolecular Chemistry. 18(11). 2051–2053. 11 indexed citations
12.
Paudyal, Mahesh P., Mingliang Wang, Yimin Hu, et al.. (2020). Intramolecular N–Me and N–H aminoetherification for the synthesis ofN-unprotected 3-amino-O-heterocycles. Organic & Biomolecular Chemistry. 19(3). 557–560. 12 indexed citations
13.
Lu, Shenci, Jun‐Yang Ong, Si Bei Poh, et al.. (2019). Practical access to axially chiral sulfonamides and biaryl amino phenols via organocatalytic atroposelective N-alkylation. Nature Communications. 10(1). 3061–3061. 102 indexed citations
14.
Kattamuri, Padmanabha V., et al.. (2019). Enantioselective Catalytic Allylation of Acyclic Ketiminoesters: Synthesis of α-Fully-Substituted Amino Esters. Organic Letters. 21(22). 9208–9211. 36 indexed citations
15.
Ma, Zhiwei, Zhe Zhou, & László Kürti. (2017). Direct and Stereospecific Synthesis of N‐H and N‐Alkyl Aziridines from Unactivated Olefins Using Hydroxylamine‐O‐Sulfonic Acids. Angewandte Chemie. 129(33). 10018–10022. 33 indexed citations
16.
Kattamuri, Padmanabha V., Jun Yin, Daniel H. Ess, et al.. (2017). Practical Singly and Doubly Electrophilic Aminating Agents: A New, More Sustainable Platform for Carbon–Nitrogen Bond Formation. Journal of the American Chemical Society. 139(32). 11184–11196. 70 indexed citations
17.
18.
Gao, Hongyin, Qing‐Long Xu, Craig Keene, et al.. (2015). Practical Organocatalytic Synthesis of Functionalized Non‐C2‐Symmetrical Atropisomeric Biaryls. Angewandte Chemie International Edition. 55(2). 566–571. 118 indexed citations
19.
Jat, Jawahar L., Mahesh P. Paudyal, Hongyin Gao, et al.. (2014). Direct Stereospecific Synthesis of Unprotected N-H and N-Me Aziridines from Olefins. Science. 343(6166). 61–65. 255 indexed citations
20.
Patel, Darshan C., Zachary S. Breitbach, Hongyin Gao, et al.. (2014). Enantiomeric separation of biaryl atropisomers using cyclofructan based chiral stationary phases. Journal of Chromatography A. 1357. 172–181. 37 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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