Esther Lete

2.3k total citations
109 papers, 1.9k citations indexed

About

Esther Lete is a scholar working on Organic Chemistry, Molecular Biology and Cancer Research. According to data from OpenAlex, Esther Lete has authored 109 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 93 papers in Organic Chemistry, 23 papers in Molecular Biology and 8 papers in Cancer Research. Recurrent topics in Esther Lete's work include Asymmetric Synthesis and Catalysis (28 papers), Chemical synthesis and alkaloids (26 papers) and Coordination Chemistry and Organometallics (25 papers). Esther Lete is often cited by papers focused on Asymmetric Synthesis and Catalysis (28 papers), Chemical synthesis and alkaloids (26 papers) and Coordination Chemistry and Organometallics (25 papers). Esther Lete collaborates with scholars based in Spain, Belgium and United States. Esther Lete's co-authors include Nuria Sotomayor, Sonia Arrasate, Esther Domı́nguez, Asier Gómez‐SanJuan, Humberto González‐Díaz, María‐Jesús Villa, Iñaki Osante, M. Isabel Collado, Eva Garcı́a and Javier Ruiz‐Sanz and has published in prestigious journals such as The Journal of Organic Chemistry, Tetrahedron and Molecules.

In The Last Decade

Esther Lete

103 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Esther Lete Spain 26 1.6k 442 209 191 179 109 1.9k
Nuria Sotomayor Spain 25 1.4k 0.9× 394 0.9× 198 0.9× 171 0.9× 142 0.8× 102 1.7k
Colin M. Tice United States 19 1.4k 0.9× 630 1.4× 109 0.5× 96 0.5× 46 0.3× 38 2.0k
Yong Seo Cho South Korea 22 809 0.5× 578 1.3× 73 0.3× 191 1.0× 60 0.3× 92 1.3k
János Wölfling Hungary 26 1.5k 1.0× 1.1k 2.4× 91 0.4× 59 0.3× 65 0.4× 156 2.2k
Jean‐François Peyrat France 28 1.6k 1.0× 559 1.3× 148 0.7× 64 0.3× 55 0.3× 70 2.1k
Sergey V. Ryabukhin Ukraine 24 1.5k 1.0× 415 0.9× 196 0.9× 98 0.5× 53 0.3× 146 1.8k
Nagaswamy Kumaragurubaran India 18 1.5k 1.0× 577 1.3× 426 2.0× 197 1.0× 57 0.3× 26 1.9k
Jean‐Yves Mérour France 26 2.0k 1.3× 775 1.8× 146 0.7× 43 0.2× 44 0.2× 98 2.3k
Oleksandr O. Grygorenko Ukraine 28 2.8k 1.8× 1.0k 2.3× 330 1.6× 272 1.4× 61 0.3× 253 3.4k
Aaron B. Beeler United States 24 1.2k 0.8× 583 1.3× 112 0.5× 45 0.2× 34 0.2× 59 1.7k

Countries citing papers authored by Esther Lete

Since Specialization
Citations

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

Fields of papers citing papers by Esther Lete

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Esther Lete

This figure shows the co-authorship network connecting the top 25 collaborators of Esther Lete. A scholar is included among the top collaborators of Esther Lete 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 Esther Lete. Esther Lete 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.
Ramis, Rafael, Aritz Leonardo, Sonia Arrasate, et al.. (2024). Identification of Riluzole derivatives as novel calmodulin inhibitors with neuroprotective activity by a joint synthesis, biosensor, and computational guided strategy. Biomedicine & Pharmacotherapy. 174. 116602–116602. 6 indexed citations
2.
Arrasate, Sonia, Cristian R. Munteanu, Carlos Fernández-Lozano, et al.. (2024). MATEO: intermolecular α-amidoalkylation theoretical enantioselectivity optimization. Online tool for selection and design of chiral catalysts and products. Journal of Cheminformatics. 16(1). 9–9. 1 indexed citations
3.
Sotomayor, Nuria, et al.. (2023). Directed C−H Allylation of Aromatic Carboxamides with Allyl Aryl Ethers under Cp*Co(III)‐Catalysis. European Journal of Organic Chemistry. 27(1). 1 indexed citations
4.
Arrasate, Sonia, Elvira Garza‐González, Verónica M. Rivas-Galindo, et al.. (2021). Molecular docking, SAR analysis and biophysical approaches in the study of the antibacterial activity of ceramides isolated from Cissus incisa. Bioorganic Chemistry. 109. 104745–104745. 7 indexed citations
5.
Arrasate, Sonia, et al.. (2021). Palladium-mediated synthesis and biological evaluation of C-10b substituted Dihydropyrrolo[1,2-b]isoquinolines as antileishmanial agents. European Journal of Medicinal Chemistry. 220. 113458–113458. 14 indexed citations
6.
Sotomayor, Nuria, et al.. (2021). Pd(II)-Catalyzed Fujiwara–Moritani Reactions for the Synthesis and Functionalization of Substituted Coumarins. ACS Omega. 6(44). 29483–29494. 9 indexed citations
7.
Fernández-Lozano, Carlos, Georgia Tsiliki, Haralambos Sarimveis, et al.. (2019). MCDCalc: Markov Chain Molecular Descriptors Calculator for Medicinal Chemistry. Current Topics in Medicinal Chemistry. 20(4). 305–317. 2 indexed citations
8.
Dı́ez-Alarcia, Rebeca, et al.. (2019). Big Data Challenges Targeting Proteins in GPCR Signaling Pathways; Combining PTML-ChEMBL Models and [35S]GTPγS Binding Assays. ACS Chemical Neuroscience. 10(11). 4476–4491. 34 indexed citations
9.
González‐Díaz, Humberto, Sonia Arrasate, A. Juan, et al.. (2014). Matrix Trace Operators: From Spectral Moments of Molecular Graphs and Complex Networks to Perturbations in Synthetic Reactions, Micelle Nanoparticles, and Drug ADME Processes. Current Drug Metabolism. 15(4). 470–488. 22 indexed citations
10.
González‐Díaz, Humberto, Sonia Arrasate, Asier Gómez‐SanJuan, et al.. (2013). General Theory for Multiple Input-Output Perturbations in Complex Molecular Systems. 1. Linear QSPR Electronegativity Models in Physical, Organic, and Medicinal Chemistry. Current Topics in Medicinal Chemistry. 13(14). 1713–1741. 84 indexed citations
11.
Gómez‐SanJuan, Asier, Nuria Sotomayor, & Esther Lete. (2013). Inter- and intramolecular enantioselective carbolithiation reactions. Beilstein Journal of Organic Chemistry. 9. 313–322. 31 indexed citations
12.
González‐Díaz, Humberto, Sonia Arrasate, Nuria Sotomayor, et al.. (2013). MIANN Models in Medicinal, Physical and Organic Chemistry. Current Topics in Medicinal Chemistry. 13(5). 619–641. 26 indexed citations
13.
Gómez‐SanJuan, Asier, et al.. (2009). Stereocontrolled conjugate additions to dihydroindolizinone systems. Synthesis of enantiopure polysubstituted tetrahydropyrrolo[2,1-a]isoquinolones. Tetrahedron. 65(29-30). 5787–5798. 8 indexed citations
14.
15.
Garcı́a, Eva, et al.. (2001). Enantioselective synthesis of pyrrolo[2,1-a]isoquinolones via stereocontrolled N-acyliminium ion cyclisations. Tetrahedron Letters. 42(8). 1511–1513. 31 indexed citations
16.
17.
Collado, M. Isabel, Esther Lete, Nuria Sotomayor, & María‐Jesús Villa. (1995). Synthesis of 5-arylpyrrolo[2,1-a]isoquinolin-3(2H)-ones from N-phenethylsuccinimides and organolithium reagents. Tetrahedron. 51(16). 4701–4710. 18 indexed citations
18.
Lete, Esther, et al.. (1993). Synthesis of PyrroloisoquinolonesviaOrganolithium Additions toN-Phenethylsuccinimides. Synlett. 1993(1). 41–42. 23 indexed citations
19.
Domı́nguez, Esther, Esther Lete, G. Germain, et al.. (1991). N-2-(2-Bromo-4,5-dimethoxyphenyl)-1-(2,3,4-trimethoxyphenyl)ethylformamide. Acta Crystallographica Section C Crystal Structure Communications. 47(10). 2115–2118.
20.
Lete, Esther, et al.. (1982). (E)-1-(2-Bromo-4,5-dimethoxyphenyl)-2-(3,4-dimethoxyphenyl)ethylene. Acta Crystallographica Section B. 38(12). 3155–3157. 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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