Renzo Luisi

6.0k total citations · 1 hit paper
179 papers, 4.6k citations indexed

About

Renzo Luisi is a scholar working on Organic Chemistry, Molecular Biology and Biomedical Engineering. According to data from OpenAlex, Renzo Luisi has authored 179 papers receiving a total of 4.6k indexed citations (citations by other indexed papers that have themselves been cited), including 163 papers in Organic Chemistry, 41 papers in Molecular Biology and 33 papers in Biomedical Engineering. Recurrent topics in Renzo Luisi's work include Synthesis and Catalytic Reactions (78 papers), Asymmetric Synthesis and Catalysis (57 papers) and Coordination Chemistry and Organometallics (39 papers). Renzo Luisi is often cited by papers focused on Synthesis and Catalytic Reactions (78 papers), Asymmetric Synthesis and Catalysis (57 papers) and Coordination Chemistry and Organometallics (39 papers). Renzo Luisi collaborates with scholars based in Italy, United Kingdom and Spain. Renzo Luisi's co-authors include Leonardo Degennaro, Saverio Florio, Vito Capriati, James A. Bull, Marco Colella, Piera Trinchera, Claudia Carlucci, Giuseppe Romanazzi, Arianna Tota and Marina Zenzola and has published in prestigious journals such as Chemical Reviews, Journal of the American Chemical Society and Chemical Society Reviews.

In The Last Decade

Renzo Luisi

168 papers receiving 4.5k citations

Hit Papers

Recent Advances in the Stereoselective Synthesis of Aziri... 2014 2026 2018 2022 2014 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Renzo Luisi Italy 35 4.0k 834 751 670 387 179 4.6k
Leonardo Degennaro Italy 30 2.7k 0.7× 649 0.8× 543 0.7× 508 0.8× 321 0.8× 100 3.2k
Jinhua J. Song United States 29 2.9k 0.7× 313 0.4× 665 0.9× 1.0k 1.5× 271 0.7× 89 3.4k
Xiu‐Qin Dong China 35 3.0k 0.7× 692 0.8× 687 0.9× 1.9k 2.9× 340 0.9× 131 3.6k
Tetsu Tsubogo Japan 20 1.6k 0.4× 514 0.6× 388 0.5× 850 1.3× 604 1.6× 34 2.2k
Ferdinando Pizzo Italy 40 3.5k 0.9× 454 0.5× 812 1.1× 478 0.7× 105 0.3× 115 3.9k
Jinxing Ye China 37 3.7k 0.9× 166 0.2× 642 0.9× 1.1k 1.6× 411 1.1× 114 4.2k
Joseph R. Martinelli United States 18 3.9k 1.0× 358 0.4× 669 0.9× 786 1.2× 135 0.3× 31 4.3k
Javier Magano United States 14 2.8k 0.7× 277 0.3× 971 1.3× 836 1.2× 127 0.3× 34 3.3k
Denis Sinou France 34 3.7k 0.9× 387 0.5× 1.2k 1.6× 1.5k 2.3× 279 0.7× 215 4.3k
Christine Fischer Germany 30 2.5k 0.6× 288 0.3× 506 0.7× 1.0k 1.5× 160 0.4× 154 3.0k

Countries citing papers authored by Renzo Luisi

Since Specialization
Citations

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

Fields of papers citing papers by Renzo Luisi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Renzo Luisi

This figure shows the co-authorship network connecting the top 25 collaborators of Renzo Luisi. A scholar is included among the top collaborators of Renzo Luisi 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 Renzo Luisi. Renzo Luisi 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.
Ford, Mark J., Katherine M. P. Wheelhouse, Philipp Natho, et al.. (2025). Towards greener-by-design fine chemicals. Part 1: synthetic frontiers. Chemical Society Reviews. 55(2). 619–674.
3.
Colella, Marco, et al.. (2025). Generation and Use of Bicyclo[1.1.0]butyllithium under Continuous Flow Conditions. Organic Letters. 27(13). 3344–3348. 3 indexed citations
4.
Natho, Philipp, Francesca Franco, Marco Colella, et al.. (2025). Novel Sulfonium Reagents for the Modular Synthesis of Spiro[2.3]Hexanes and Heteroatom‐Containing Analogues: Synthesis, Application, and Evaluation as Bioisosteres. Angewandte Chemie International Edition. 65(5). e21633–e21633.
5.
Ford, Mark J., Marco Uboldi, Alice Melocchi, et al.. (2025). Towards greener-by-design fine chemicals. Part 2: technological frontiers. Chemical Society Reviews. 55(2). 675–713.
7.
Andresini, Michael, et al.. (2024). Synthesis of Aza‐S(VI) Fluorides and Primary Sulfonimidamides from Sulfinylamines. Advanced Synthesis & Catalysis. 367(2). 6 indexed citations
8.
Natho, Philipp, Michael Andresini, Ernesto Mesto, et al.. (2024). 1‐Oxa‐2,6‐Diazaspiro[3.3]heptane as a New Potential Piperazine Bioisostere – Flow‐Assisted Preparation and Derivatisation by Strain‐Release of Azabicyclo[1.1.0]butanes. Advanced Synthesis & Catalysis. 366(18). 3894–3902. 6 indexed citations
9.
Luisi, Renzo, et al.. (2024). A Practical Guide to SuFEx Chemistry: An Overview of S(VI)-SuFEx Linkers and Their Reactivity. Synthesis. 57(9). 1569–1582. 8 indexed citations
10.
Luisi, Renzo & James A. Bull. (2023). Synthesis of Sulfoximines and Sulfonimidamides Using Hypervalent Iodine Mediated NH Transfer. Molecules. 28(3). 1120–1120. 27 indexed citations
11.
Luisi, Renzo, et al.. (2022). Synthesis and Characterization of Novel Heterocyclic Chalcones from 1-Phenyl-1H-pyrazol-3-ol. Molecules. 27(12). 3752–3752. 12 indexed citations
12.
13.
Takahashi, Yusuke, Yosuke Ashikari, Masahiro Takumi, et al.. (2019). Synthesis of Biaryls Having a Piperidylmethyl Group Based on Space Integration of Lithiation, Borylation, and Suzuki–Miyaura Coupling. European Journal of Organic Chemistry. 2020(5). 618–622. 18 indexed citations
14.
Colella, Marco, Claudia Carlucci, & Renzo Luisi. (2018). Supported Catalysts for Continuous Flow Synthesis. Topics in Current Chemistry. 376(6). 46–46. 40 indexed citations
15.
Romanazzi, Giuseppe, Leonardo Degennaro, Piero Mastrorilli, & Renzo Luisi. (2017). Chiral Switchable Catalysts for Dynamic Control of Enantioselectivity. ACS Catalysis. 7(6). 4100–4114. 60 indexed citations
16.
Parisi, Giovanna, Leonardo Degennaro, Claudia Carlucci, et al.. (2017). A greener and efficient access to substituted four- and six-membered sulfur-bearing heterocycles. Organic & Biomolecular Chemistry. 15(23). 5000–5015. 17 indexed citations
17.
Pisano, Luisa, Leonardo Degennaro, Massimo Carraro, et al.. (2016). Computational NMR as Useful Tool for Predicting Structure and Stereochemistry of Four‐Membered Sulfur Heterocycles. European Journal of Organic Chemistry. 2016(19). 3252–3258. 7 indexed citations
18.
Luisi, Renzo & Vito Capriati. (2014). Lithium compounds in organic synthesis : from fundamentals to applications. Wiley-VCH eBooks. 50 indexed citations
19.
Degennaro, Leonardo, et al.. (2014). External Trapping of Halomethyllithium Enabled by Flow Microreactors. Advanced Synthesis & Catalysis. 357(1). 21–27. 55 indexed citations
20.
Trinchera, Piera, Biagia Musio, Leonardo Degennaro, et al.. (2012). One-pot preparation of piperazines by regioselective ring-opening of non-activated arylaziridines. Organic & Biomolecular Chemistry. 10(10). 1962–1962. 14 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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