Jaume Vilarrasa

4.8k total citations
171 papers, 3.7k citations indexed

About

Jaume Vilarrasa is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, Jaume Vilarrasa has authored 171 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 139 papers in Organic Chemistry, 62 papers in Molecular Biology and 25 papers in Inorganic Chemistry. Recurrent topics in Jaume Vilarrasa's work include Chemical Synthesis and Analysis (41 papers), Synthetic Organic Chemistry Methods (39 papers) and Asymmetric Synthesis and Catalysis (35 papers). Jaume Vilarrasa is often cited by papers focused on Chemical Synthesis and Analysis (41 papers), Synthetic Organic Chemistry Methods (39 papers) and Asymmetric Synthesis and Catalysis (35 papers). Jaume Vilarrasa collaborates with scholars based in Spain, France and Switzerland. Jaume Vilarrasa's co-authors include Fèlix Urpı́, Anna M. Costa, Pedro Romea, Jordi García, Xavier Ariza, Alejandro Castro‐Álvarez, Jaume Farràs, Jordi Burés, Ramon Berenguer and Santiago Olivella and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Nucleic Acids Research.

In The Last Decade

Jaume Vilarrasa

170 papers receiving 3.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jaume Vilarrasa Spain 34 2.7k 1.4k 371 224 209 171 3.7k
G. Sudhakar Reddy India 27 2.4k 0.9× 936 0.7× 404 1.1× 153 0.7× 292 1.4× 102 3.3k
Jacques Lebreton France 31 2.3k 0.9× 1.7k 1.2× 290 0.8× 167 0.7× 105 0.5× 175 3.7k
Willem A. L. van Otterlo South Africa 32 2.8k 1.0× 1.1k 0.8× 351 0.9× 352 1.6× 117 0.6× 147 3.8k
Kang Zhao China 46 4.8k 1.8× 1.1k 0.8× 445 1.2× 391 1.7× 132 0.6× 202 6.6k
M. Luísa Jimeno Spain 31 1.5k 0.6× 995 0.7× 191 0.5× 292 1.3× 175 0.8× 180 3.1k
Ian D. Jenkins Australia 27 1.9k 0.7× 901 0.6× 360 1.0× 129 0.6× 76 0.4× 165 2.6k
James L. Gleason Canada 28 2.4k 0.9× 1.0k 0.7× 471 1.3× 254 1.1× 75 0.4× 79 3.1k
Robert S. Coleman United States 36 2.3k 0.9× 1.8k 1.3× 121 0.3× 307 1.4× 84 0.4× 106 3.5k
L. Todaro United States 29 1.2k 0.4× 788 0.6× 422 1.1× 228 1.0× 141 0.7× 74 2.2k
Daniel Bur Switzerland 32 1.0k 0.4× 1.5k 1.0× 179 0.5× 138 0.6× 161 0.8× 88 2.9k

Countries citing papers authored by Jaume Vilarrasa

Since Specialization
Citations

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

Fields of papers citing papers by Jaume Vilarrasa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jaume Vilarrasa

This figure shows the co-authorship network connecting the top 25 collaborators of Jaume Vilarrasa. A scholar is included among the top collaborators of Jaume Vilarrasa 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 Jaume Vilarrasa. Jaume Vilarrasa 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.
Vilarrasa, Jaume, et al.. (2017). Computer-Aided Insight into the Relative Stability of Enamines. Synthesis. 49(24). 5285–5306. 17 indexed citations
2.
Gómez, Alex Joffre Quimis, et al.. (2014). A synthetic approach to palmerolides via Negishi cross coupling. The challenge of the C15–C16 bond formation. Tetrahedron Letters. 55(33). 4623–4627. 8 indexed citations
3.
Mouscadet, Jean‐François, et al.. (2010). Synthesis of benzo-, pyrido-, thieno- and imidazo-fused N-hydroxy-4-oxopyrimidine-2-carboxylic acid derivatives. Tetrahedron Letters. 52(7). 753–756. 1 indexed citations
4.
Vendeix, Franck A. P., Richard Guenther, Andrzej Małkiewicz, et al.. (2009). The structure of the human tRNALys3 anticodon bound to the HIV genome is stabilized by modified nucleosides and adjacent mismatch base pairs. Nucleic Acids Research. 37(10). 3342–3353. 41 indexed citations
5.
Burés, Jordi, et al.. (2008). Seebach’s oxazolidinone is a good catalyst for aldol reactions. Tetrahedron Letters. 49(37). 5414–5418. 42 indexed citations
6.
Vilarrasa, Jaume, et al.. (2007). Cu2(OTf)2‐Catalyzed and Microwave‐Controlled Preparation of Tetrazoles from Nitriles and Organic Azides under Mild, Safe Conditions. Angewandte Chemie International Edition. 46(21). 3926–3930. 94 indexed citations
7.
Jensen, Søren Skov, Xavier Ariza, Poul Nielsen, Jaume Vilarrasa, & Finn Kirpekar. (2006). Collision‐induced dissociation of cytidine and its derivatives. Journal of Mass Spectrometry. 42(1). 49–57. 34 indexed citations
8.
Pineda, Oriol, Jaume Farràs, Laura Maccari, et al.. (2004). Computational comparison of microtubule-stabilising agents laulimalide and peloruside with taxol and colchicine. Bioorganic & Medicinal Chemistry Letters. 14(19). 4825–4829. 54 indexed citations
9.
Ariza, Xavier, et al.. (2000). 1,2-ジオールの新しい保護基(Boc-およびMoc-エチリデン) アセタールの塩基による開裂. Organic Letters. 2(18). 2809–2811. 1 indexed citations
10.
Ariza, Xavier, et al.. (2000). New Protecting Groups for 1,2-Diols (Boc- and Moc-ethylidene). Cleavage of Acetals with Bases. Organic Letters. 2(18). 2809–2811. 22 indexed citations
11.
Serra, Carmen, Jaume Farràs, & Jaume Vilarrasa. (1999). Cyclic sulfates as synthetic equivalents of α-epoxynucleosides. Tetrahedron Letters. 40(51). 9111–9113. 6 indexed citations
12.
Serra, Carmen, et al.. (1998). Stabilisation of pyrimidine nucleoside triflates by N-nitro groups. Tetrahedron Letters. 39(41). 7575–7578. 13 indexed citations
13.
Ariza, Xavier, Jaume Farràs, Carmen Serra, & Jaume Vilarrasa. (1997). N-Nitration, 15N-Labeling, and N-to-N Linking of Hydroxyl-Silylated Pyrimidine Nucleosides. The Journal of Organic Chemistry. 62(5). 1547–1549. 20 indexed citations
14.
Ariza, Xavier, et al.. (1995). A New Route to 15N-Labeled, N-Alkyl, and N-Amino Nucleosides via N-Nitration of Uridines and Inosines. Journal of the American Chemical Society. 117(13). 3665–3673. 57 indexed citations
15.
Ariza, Xavier, et al.. (1992). Azide- or fluorine-containing 2′ & 3′-azolyluridines by regioselective opening of 1-(2′,3′-anhydro-β-d-lyxofuranosyl)uracils. Tetrahedron Letters. 33(28). 4069–4072. 10 indexed citations
16.
Sanz, Javier Fdez., et al.. (1989). ChemInform Abstract: AM1 Study of the Protonation of Pteridine‐Related Tetraazanaphthalenes.. ChemInform. 20(4). 1 indexed citations
17.
Farràs, Jaume, et al.. (1986). 4-31G ab initio and MNDO semi-empirical calculations on bicyclic CN7–and N8species, and n.m.r. and i.r. studies on15N-labelled CN7–. Journal of the Chemical Society Chemical Communications. 959–961. 12 indexed citations
18.
Farràs, Jaume & Jaume Vilarrasa. (1986). Nitrene-like behaviour of diazoazoles?. Journal of the Chemical Society Chemical Communications. 1127–1129. 2 indexed citations
19.
Granell, Jaume, Joaquim Sales, & Jaume Vilarrasa. (1984). Reactivity of dimetallated benzalazines. Transition Metal Chemistry. 9(6). 203–205. 9 indexed citations
20.
García, Jordi, et al.. (1984). Nitrosation of peptide bonds. Cleavage of nitrosated peptides by pyrrolidine and α-amino esters. Tetrahedron. 40(16). 3121–3127. 26 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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