Josep Font

3.7k total citations
179 papers, 3.0k citations indexed

About

Josep Font is a scholar working on Organic Chemistry, Molecular Biology and Pharmaceutical Science. According to data from OpenAlex, Josep Font has authored 179 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 147 papers in Organic Chemistry, 44 papers in Molecular Biology and 22 papers in Pharmaceutical Science. Recurrent topics in Josep Font's work include Asymmetric Synthesis and Catalysis (43 papers), Organic Chemistry Cycloaddition Reactions (41 papers) and Oxidative Organic Chemistry Reactions (27 papers). Josep Font is often cited by papers focused on Asymmetric Synthesis and Catalysis (43 papers), Organic Chemistry Cycloaddition Reactions (41 papers) and Oxidative Organic Chemistry Reactions (27 papers). Josep Font collaborates with scholars based in Spain, United Kingdom and United States. Josep Font's co-authors include Marta Figueredo, Pedro de March, Rosa M. Ortuño, Ramón Alibés, J.L. Bourdelande, Félix Busquè, Teodor Parella, Ángel Álvarez‐Larena, Pau Bayón and Pelayo Camps and has published in prestigious journals such as Journal of the American Chemical Society, SHILAP Revista de lepidopterología and Journal of Materials Chemistry.

In The Last Decade

Josep Font

177 papers receiving 2.9k citations

Peers

Josep Font

BIOCH

Rick Danheiser United States

Willi M. Amberg Switzerland

Yoo Tanabe Japan

Michael Chaykovsky United States

Derrick L. J. Clive Canada

Masazumi Ikeda Japan

Harold W. Moore United States

Sigeru Torii Japan

Tse‐Lok Ho Canada

Russell J. Linderman United States

Rick Danheiser United States

Josep Font

4.7k ×1.9

689 ×1.0

241 ×0.9

185 ×0.7

127 ×0.6

BIOCH

Citations per year, relative to Josep Font Josep Font (= 1×) peers Rick Danheiser

Countries citing papers authored by Josep Font

Since Specialization

Citations

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

Fields of papers citing papers by Josep Font

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Josep Font

This figure shows the co-authorship network connecting the top 25 collaborators of Josep Font. A scholar is included among the top collaborators of Josep Font 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 Josep Font. Josep Font is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Flores, Ramón, Félix Busquè, Marta Figueredo, et al.. (2012). Synthesis, Anti‐HIV Activity Studies, and in silico Rationalization of Cyclobutane‐Fused Nucleosides. ChemMedChem. 7(6). 1044–1056. 7 indexed citations

Alibés, Ramón, et al.. (2011). Divergent Approach to Gabosines and Anhydrogabosines: Enantioselective Syntheses of (+)‐Epiepoformin, (+)‐EpoKformin, (+)‐Gabosine A, and Gabosines B and F. European Journal of Organic Chemistry. 2011(8). 1534–1543. 28 indexed citations

Alibés, Ramón & Josep Font. (2007). Cyclobutanes and cyclobutenes through [2+2] photocycloadditions to &, B- unsaturated y-lactones. Afinidad. 64(528). 189–197. 2 indexed citations

Alibés, Ramón, Pau Bayón, Pedro de March, et al.. (2005). An Effective Enantioselective Approach to the Securinega Alkaloids: Total Synthesis of (−)-Norsecurinine. Organic Letters. 7(22). 5107–5109. 43 indexed citations

Busquè, Félix, et al.. (2004). A Study of the Conjugate Addition of Thionucleophiles to 2(5H)‐Furanones. European Journal of Organic Chemistry. 2004(7). 1492–1499. 21 indexed citations

March, Pedro de, et al.. (2003). C₂-Symmetric Enantiopure Ethanotethered Bis(α,β-butenolides) as Templates for Asymmetric Synthesis. Application to the Synthesis of (+)-Grandisol¹. The Journal of Organic Chemistry. 68(6). 2437–2447. 40 indexed citations

Alibés, Ramón, Pedro de March, Marta Figueredo, et al.. (2003). Photochemical [2 + 2] Cycloaddition of Acetylene to Chiral 2(5H)-Furanones. The Journal of Organic Chemistry. 68(4). 1283–1289. 19 indexed citations

Alibés, Ramón, Félix Busquè, Pedro de March, et al.. (2001). Acetals of γ-oxo-α,β-unsaturated esters in nitrone cycloadditions. Regio- and stereochemical implications. Tetrahedron Asymmetry. 12(12). 1747–1756. 6 indexed citations

Prat, Ferran, Cristina Martí, Santi Nonell, et al.. (2001). C60 Fullerene-based materials as singlet oxygen O2(1Δg) photosensitizers: a time-resolved near-IR luminescence and optoacoustic study. Physical Chemistry Chemical Physics. 3(9). 1638–1643. 36 indexed citations

10.

March, Pedro de, et al.. (2000). New, highly efficient syntheses of rac-, (R)- and (S)-4-hydroxy-2-cyclohexenone. Tetrahedron Asymmetry. 11(22). 4473–4483. 24 indexed citations

11.

Bayón, Pau, Pedro de March, M. A. Espinosa, Marta Figueredo, & Josep Font. (2000). Use of chiral Ti(IV) complexes in the cycloaddition of C,N-diphenylnitrone to tert-butyl vinyl ether. Tetrahedron Asymmetry. 11(8). 1757–1765. 15 indexed citations

12.

Busquè, Félix, et al.. (1998). Diastereofacial Selectivity in the Cycloaddition of Nitrones to (E)-γ-Oxygenated α,β-Unsaturated Esters. The Journal of Organic Chemistry. 63(6). 2052–2052. 2 indexed citations

13.

March, Pedro de, et al.. (1998). First examples of nitrile ylid cycloadditions to α,β-unsaturated lactones. Tetrahedron. 54(38). 11613–11622. 9 indexed citations

14.

Domingo, C., Josep Font, C. Baixeras, & F. Fernández. (1996). Source abundances of ultra heavy elements derived from UHCRE measurements. Radiation Measurements. 26(6). 825–832. 4 indexed citations

15.

Bourdelande, J.L., et al.. (1996). Photophysical studies on solid C60 using diffuse reflectance laser flash photolysis (DRLFP). Journal of Photochemistry and Photobiology A Chemistry. 98(3). 127–128. 4 indexed citations

16.

Rauter, Amélia P., et al.. (1995). Synthetic, Fungicidal Unsaturated-γ-lactones Attached to Furanosidic Systems. Configurational Determination by Nuclear Overhauser Effect ¹. Journal of Carbohydrate Chemistry. 14(7). 929–948. 13 indexed citations

17.

Font, Josep, et al.. (1992). ChemInform Abstract: Synthesis of Bromobutenolides. An Approach to the Synthesis of Fimbrolides. ChemInform. 23(19). 1 indexed citations

18.

Font, Josep, et al.. (1982). Studies on structurally simple α,β-butenolides—I. Tetrahedron. 38(15). 2377–2394. 52 indexed citations

19.

Font, Josep, et al.. (1969). An approach to the synthesis of 1,2-dialkoxyacetylenes benzyne intermediates. Tetrahedron Letters. 10(54). 4743–4744. 5 indexed citations

20.

Strausz, O. P., et al.. (1968). Formation and reactions of monovalent carbon intermediates. II. Further studies on the decomposition of diethyl mercurybisdiazoacetate. Journal of the American Chemical Society. 90(7). 1930–1931. 35 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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