Josep Bonjoch

4.8k total citations
177 papers, 4.0k citations indexed

About

Josep Bonjoch is a scholar working on Organic Chemistry, Pharmacology and Molecular Biology. According to data from OpenAlex, Josep Bonjoch has authored 177 papers receiving a total of 4.0k indexed citations (citations by other indexed papers that have themselves been cited), including 161 papers in Organic Chemistry, 48 papers in Pharmacology and 27 papers in Molecular Biology. Recurrent topics in Josep Bonjoch's work include Chemical synthesis and alkaloids (60 papers), Asymmetric Synthesis and Catalysis (41 papers) and Advanced Synthetic Organic Chemistry (40 papers). Josep Bonjoch is often cited by papers focused on Chemical synthesis and alkaloids (60 papers), Asymmetric Synthesis and Catalysis (41 papers) and Advanced Synthetic Organic Chemistry (40 papers). Josep Bonjoch collaborates with scholars based in Spain, Switzerland and United Kingdom. Josep Bonjoch's co-authors include Daniel Solé, Joan Bosch, Ben Bradshaw, Fai͏̈za Diaba, Nativitat Valls, Josefina Quirante, Emma Peidró, L. Vallverdu, Silvina García-Rubio and Núria Casamitjana and has published in prestigious journals such as Chemical Reviews, Journal of the American Chemical Society and Angewandte Chemie International Edition.

In The Last Decade

Josep Bonjoch

172 papers receiving 3.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Josep Bonjoch Spain 37 3.6k 843 618 334 274 177 4.0k
Joan Bosch Spain 37 5.4k 1.5× 1.3k 1.6× 1.1k 1.8× 323 1.0× 223 0.8× 318 5.8k
David Y.‐K. Chen Singapore 37 4.1k 1.2× 499 0.6× 939 1.5× 755 2.3× 761 2.8× 99 4.9k
Noritaka Chida Japan 40 3.9k 1.1× 569 0.7× 1.5k 2.4× 513 1.5× 346 1.3× 170 4.3k
Yanxing Jia China 36 3.2k 0.9× 526 0.6× 657 1.1× 425 1.3× 422 1.5× 118 3.8k
Chihiro Kibayashi Japan 40 3.8k 1.1× 287 0.3× 1.1k 1.7× 399 1.2× 365 1.3× 150 4.2k
Christopher D. Vanderwal United States 36 2.8k 0.8× 362 0.4× 791 1.3× 388 1.2× 443 1.6× 105 3.5k
Thomas R. R. Pettus United States 33 3.2k 0.9× 266 0.3× 676 1.1× 461 1.4× 394 1.4× 79 3.7k
Kozo Shishido Japan 35 3.4k 1.0× 219 0.3× 854 1.4× 370 1.1× 355 1.3× 219 4.0k
A. Chiaroni France 33 2.6k 0.7× 280 0.3× 1.2k 1.9× 382 1.1× 214 0.8× 208 3.5k
James H. Rigby United States 34 2.9k 0.8× 260 0.3× 482 0.8× 198 0.6× 195 0.7× 124 3.1k

Countries citing papers authored by Josep Bonjoch

Since Specialization
Citations

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

Fields of papers citing papers by Josep Bonjoch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Josep Bonjoch

This figure shows the co-authorship network connecting the top 25 collaborators of Josep Bonjoch. A scholar is included among the top collaborators of Josep Bonjoch 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 Bonjoch. Josep Bonjoch 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.
Bonjoch, Josep, et al.. (2025). Merging carboxylic acids with metal-catalyzed hydrogen atom transfer (MHAT) chemistry via alkene-functionalized redox-active esters. Chemical Science. 16(34). 15478–15485. 1 indexed citations
2.
Bonjoch, Josep, et al.. (2024). Metal-Catalyzed Hydrogen Atom Transfer (MHAT) Hydroalkylation with Electron-Deficient Alkynes. Organic Letters. 26(49). 10553–10558. 3 indexed citations
3.
Bonjoch, Josep, et al.. (2023). Synthesis of Alkaloids and Compounds Containing the 3,4‐Benzomorphan Scaffold. European Journal of Organic Chemistry. 27(1). 2 indexed citations
4.
Ciudad, Carlos J., et al.. (2022). Base-Mediated Nitrophenyl Reductive Cyclization for the Synthesis of Hexahydro-2,6-methano-1-benzazocines. The Journal of Organic Chemistry. 87(22). 15693–15702. 3 indexed citations
5.
Bonjoch, Josep, et al.. (2019). Iron Hydride Radical Reductive Alkylation of Unactivated Alkenes. Organic Letters. 22(2). 684–688. 27 indexed citations
6.
Bradshaw, Ben, et al.. (2014). A gram-scale route to phlegmarine alkaloids: rapid total synthesis of (−)-cermizine B. Chemical Communications. 50(54). 7099–7102. 36 indexed citations
7.
8.
Marín, M. Luisa, Ramón J. Zaragozá, Miguel A. Miranda, Fai͏̈za Diaba, & Josep Bonjoch. (2011). Translocation versus cyclisation in radicals derived from N-3-alkenyl trichloroacetamides. Organic & Biomolecular Chemistry. 9(9). 3180–3180. 5 indexed citations
9.
Bonjoch, Josep, et al.. (2009). Synthesis and structure–activity relationships of γ-carboline derivatives as potent and selective cysLT1 antagonists. Bioorganic & Medicinal Chemistry Letters. 19(15). 4299–4302. 16 indexed citations
10.
Bradshaw, Ben, et al.. (2008). Fischer indolization of octahydroindol-6-one derivatives revisited: diastereoisomerization and racemization processes. Tetrahedron Asymmetry. 19(18). 2130–2134. 1 indexed citations
11.
Diaba, Fai͏̈za, et al.. (2006). Synthesis of enantiopure 1-azaspiro[4.5]dec-6-en-8-ones from l-proline derivatives. Tetrahedron Asymmetry. 17(9). 1437–1443. 11 indexed citations
12.
Solé, Daniel, L. Vallverdu, Xavier Soláns, Mercè Font-Bardı́a, & Josep Bonjoch. (2003). Intramolecular Pd-Mediated Processes of Amino-Tethered Aryl Halides and Ketones:  Insight into the Ketone α-Arylation and Carbonyl-Addition Dichotomy. A New Class of Four-Membered Azapalladacycles. Journal of the American Chemical Society. 125(6). 1587–1594. 147 indexed citations
13.
Valls, Nativitat, et al.. (2003). Syntheses of Both the Putative and Revised Structures of Aeruginosin EI461 Bearing a New Bicyclic α-Amino Acid. Organic Letters. 5(4). 447–450. 42 indexed citations
14.
Bonjoch, Josep, et al.. (2003). A new synthetic entry to the tricyclic skeleton of FR901483 by palladium-catalyzed cyclization of vinyl bromides with ketone enolates. Tetrahedron Letters. 44(46). 8387–8390. 36 indexed citations
15.
16.
Bonjoch, Josep, Josefina Quirante, Carmen Escolano, & Fai͏̈za Diaba. (1999). A Radical Route to Morphans. Synthesis and Spectroscopic Data of the 2-Azabicyclo[3.3.1]nonane. Heterocycles. 50(2). 731–731. 10 indexed citations
17.
18.
Bonjoch, Josep, et al.. (1996). Synthesis of the octahydroindole core of aeruginosins: a new bicyclic α-amino acid. Tetrahedron Asymmetry. 7(7). 1899–1902. 28 indexed citations
19.
Casamitjana, Núria, Jordi Gracia Gracia, Josep Bonjoch, & Joan Bosch. (1992). Studies on the Synthesis of Strychnos Indole Alkaloids. An Efficient Stereocontrolled Synthetic Route to 2,4,8- and 2,8,9-Trisubstituted 2-Azabicyclo[3.3.1]nonan-7-ones. Tetrahedron Letters. 33(15). 2055–2058. 2 indexed citations
20.
Bonjoch, Josep, et al.. (1984). 1,2,3,5,6,10b‐ヘキサヒドロピロロ〔2,1‐a〕イソキノリン類 3‐ベンジル誘導体の調製と立体化学. Heterocycles. 22(4). 767–772. 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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