Manuel Gómez-Guillén

415 total citations
38 papers, 317 citations indexed

About

Manuel Gómez-Guillén is a scholar working on Organic Chemistry, Molecular Biology and Pharmaceutical Science. According to data from OpenAlex, Manuel Gómez-Guillén has authored 38 papers receiving a total of 317 indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Organic Chemistry, 21 papers in Molecular Biology and 10 papers in Pharmaceutical Science. Recurrent topics in Manuel Gómez-Guillén's work include Carbohydrate Chemistry and Synthesis (28 papers), Glycosylation and Glycoproteins Research (12 papers) and Fluorine in Organic Chemistry (9 papers). Manuel Gómez-Guillén is often cited by papers focused on Carbohydrate Chemistry and Synthesis (28 papers), Glycosylation and Glycoproteins Research (12 papers) and Fluorine in Organic Chemistry (9 papers). Manuel Gómez-Guillén collaborates with scholars based in Spain, Switzerland and United States. Manuel Gómez-Guillén's co-authors include Francisca Cabrera‐Escribano, José M. Lassaletta, Ana T. Carmona, Antonio Gómez-Sánchez, M. J. Diáñez, A. Lopéz-Castro, Juan A. Galbis, Francisco García González, F. Madrid and Antonio Franconetti and has published in prestigious journals such as Physical Chemistry Chemical Physics, Tetrahedron Letters and Carbohydrate Research.

In The Last Decade

Manuel Gómez-Guillén

36 papers receiving 306 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Manuel Gómez-Guillén Spain 12 274 150 58 22 16 38 317
Ian Shepperson United Kingdom 10 405 1.5× 81 0.5× 86 1.5× 36 1.6× 18 1.1× 11 500
Henning Lütjens Germany 11 404 1.5× 127 0.8× 41 0.7× 20 0.9× 13 0.8× 11 482
Paolo Zani Italy 13 354 1.3× 61 0.4× 34 0.6× 25 1.1× 7 0.4× 43 400
В. С. Мокрушин Russia 11 484 1.8× 129 0.9× 25 0.4× 22 1.0× 22 1.4× 85 552
Alexey V. Kletskov Belarus 12 303 1.1× 90 0.6× 34 0.6× 11 0.5× 10 0.6× 43 365
A. M. Moiseenkov Russia 7 211 0.8× 83 0.6× 15 0.3× 28 1.3× 29 1.8× 98 278
S. NISHII Japan 13 438 1.6× 161 1.1× 20 0.3× 26 1.2× 14 0.9× 21 483
Mark S. Cooper United Kingdom 5 275 1.0× 103 0.7× 16 0.3× 27 1.2× 21 1.3× 6 378
Andrzej Zarecki Poland 9 281 1.0× 84 0.6× 26 0.4× 15 0.7× 16 1.0× 14 319
Majid M. Sadeghi Iran 14 449 1.6× 123 0.8× 49 0.8× 24 1.1× 8 0.5× 37 512

Countries citing papers authored by Manuel Gómez-Guillén

Since Specialization
Citations

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

Fields of papers citing papers by Manuel Gómez-Guillén

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Manuel Gómez-Guillén. 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 Manuel Gómez-Guillén. The network helps show where Manuel Gómez-Guillén may publish in the future.

Co-authorship network of co-authors of Manuel Gómez-Guillén

This figure shows the co-authorship network connecting the top 25 collaborators of Manuel Gómez-Guillén. A scholar is included among the top collaborators of Manuel Gómez-Guillén 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 Manuel Gómez-Guillén. Manuel Gómez-Guillén 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.
Franconetti, Antonio, et al.. (2014). Electronically tunable anion−π interactions in pyrylium complexes: experimental and theoretical studies. Physical Chemistry Chemical Physics. 16(34). 18442–18442. 13 indexed citations
2.
Franconetti, Antonio, et al.. (2012). Synthesis of cyclically constrained sugar derived α/β- and α/γ-peptides. Organic & Biomolecular Chemistry. 11(4). 676–686. 8 indexed citations
3.
Cabrera‐Escribano, Francisca, et al.. (2010). Synthesis of Conformationally Restricted Glycoamino Acids using Fluorinating Agents. 381–381. 1 indexed citations
4.
Cabrera‐Escribano, Francisca, et al.. (2009). Easy Access to Configurationally Controlled C-Glycofuranoside-Based Building Blocks by Means of Formyl C-Glycofuranosides. Synlett. 2010(2). 271–275. 1 indexed citations
5.
Cabrera‐Escribano, Francisca, et al.. (2006). A Novel Approach to the Synthesis of N‐Substituted 1‐C‐Aminomethyl Glycofuranosides.. ChemInform. 37(20). 1 indexed citations
6.
Cabrera‐Escribano, Francisca, et al.. (2005). A short and highly stereoselective route to polyhydroxy-perhydroazaazulenes via a C-(d-galacto-pentopyranos-5-yl)isoxazolidine. Tetrahedron Asymmetry. 16(23). 3897–3907. 11 indexed citations
7.
Cabrera‐Escribano, Francisca, et al.. (2004). Fluorination of 2-hydroxy-hexopyranosides by DAST: towards formyl C-glycofuranosides from equatorial-2-OH methyl hexopyranosides. Tetrahedron Asymmetry. 15(3). 429–444. 19 indexed citations
8.
Cabrera‐Escribano, Francisca, et al.. (2004). Stereoselective synthesis of 3-glycosyl-5-methoxycarbonyl-isoxazolidines from d-galactose and d-glucose. Tetrahedron Letters. 45(25). 4835–4839. 2 indexed citations
9.
Cabrera‐Escribano, Francisca, et al.. (1997). Novel rearrangement reactions in the fluorination of methyl 3-C-methyl-3-nitro-α-l-hexopyranosides by the DAST reagent. Tetrahedron Letters. 38(7). 1231–1234. 15 indexed citations
10.
Cabrera‐Escribano, Francisca, et al.. (1996). 1,3-Dicarbonyl sugar derivatives from sugar nitro-olefins. Carbohydrate Research. 285. 49–58. 6 indexed citations
11.
Diáñez, M. J., et al.. (1995). Silica gel-catalysed addition of methyl nitroacetate to 1,2: 3,4--O--galacto- and 2,3-O-. Crystal structure of methyl 7--O--threo-α--galacto-. Carbohydrate Research. 271(1). 79–99. 5 indexed citations
12.
13.
Gómez-Guillén, Manuel & José M. Lassaletta. (1993). 5- and 4-(d-lyxofuranosyl)pyrazoles: a new type of pyrazole C-nucleoside. Carbohydrate Research. 239. 279–284. 2 indexed citations
14.
15.
Gómez-Guillén, Manuel, et al.. (1990). Cyclodehydration of 3-(d-manno-pentitol-1-yl)pyrazoles: Synthesis of 3-(d-arabinofuranosyl)pyrazoles. Carbohydrate Research. 201(2). 233–240. 6 indexed citations
16.
Gómez-Guillén, Manuel, et al.. (1982). Reaction of d-mannose arylhydrazones with dimethyl acetylenedicarboxylate: Synthesis of pentahydroxypentylpyrazoles. Carbohydrate Research. 108(1). 51–58. 2 indexed citations
17.
González, Francisco García, et al.. (1980). Reaction of 2-amino-2-deoxyheptoses with cyclic β-dicarbonyl compounds. Carbohydrate Research. 78(1). 17–23. 10 indexed citations
18.
González, Francisco García, et al.. (1980). Preparation of new C-nucleosides by intramolecular dehydration of 2-pentahydroxypentyl-4,5,6,7-tetrahydroindol-4-ones. Carbohydrate Research. 80(1). 37–43. 12 indexed citations
19.
Galbis, Juan A., et al.. (1979). Síntesis de 2-amin0-2-desoxi-heptosas por el método del aminonitrilo. 75. 387–391.
20.
Sánchez, Antonio, et al.. (1974). Synthesis of 1,5,6,7-tetrahydroindol-4-ones from amino-sugars and cyclohexane-1,3-diones. Journal of the Chemical Society Perkin Transactions 1. 1237–1243. 6 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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