Tommaso Marcelli

2.8k total citations
34 papers, 2.5k citations indexed

About

Tommaso Marcelli is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, Tommaso Marcelli has authored 34 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Organic Chemistry, 12 papers in Molecular Biology and 8 papers in Inorganic Chemistry. Recurrent topics in Tommaso Marcelli's work include Asymmetric Synthesis and Catalysis (16 papers), Chemical Synthesis and Analysis (12 papers) and Asymmetric Hydrogenation and Catalysis (8 papers). Tommaso Marcelli is often cited by papers focused on Asymmetric Synthesis and Catalysis (16 papers), Chemical Synthesis and Analysis (12 papers) and Asymmetric Hydrogenation and Catalysis (8 papers). Tommaso Marcelli collaborates with scholars based in Italy, Netherlands and United Kingdom. Tommaso Marcelli's co-authors include Henk Hiemstra, Jan H. van Maarseveen, Fahmi Himo, Richard N. S. van der Haas, Peter Hammar, Jonathan Clayden, Jordi Solà, Martin Lutz, Anthony L. Spek and Robert A. Brown and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and ACS Catalysis.

In The Last Decade

Tommaso Marcelli

33 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tommaso Marcelli Italy 22 2.2k 719 600 260 122 34 2.5k
Tomotaka Okino Japan 11 4.1k 1.9× 1.1k 1.5× 1.2k 2.0× 317 1.2× 199 1.6× 11 4.3k
Stephan J. Zuend United States 14 1.4k 0.6× 387 0.5× 511 0.9× 146 0.6× 58 0.5× 16 1.7k
Mark D. Levin United States 22 2.5k 1.2× 569 0.8× 602 1.0× 191 0.7× 290 2.4× 40 3.1k
Yoshihiro Sohtome Japan 27 2.0k 0.9× 662 0.9× 675 1.1× 206 0.8× 81 0.7× 66 2.4k
Tummanapalli Satyanarayana India 11 2.3k 1.0× 647 0.9× 440 0.7× 219 0.8× 60 0.5× 21 2.5k
Boris J. Nachtsheim Germany 34 4.0k 1.8× 481 0.7× 945 1.6× 175 0.7× 208 1.7× 84 4.3k
Henrik Sundén Sweden 39 4.0k 1.8× 923 1.3× 920 1.5× 147 0.6× 110 0.9× 92 4.5k
Jerry A. Murry United States 28 2.4k 1.1× 526 0.7× 571 1.0× 159 0.6× 85 0.7× 53 2.7k
Carlos Valdés Spain 40 5.4k 2.5× 446 0.6× 485 0.8× 162 0.6× 272 2.2× 109 5.6k
Travis Dudding Canada 32 3.0k 1.4× 727 1.0× 961 1.6× 149 0.6× 260 2.1× 121 3.4k

Countries citing papers authored by Tommaso Marcelli

Since Specialization
Citations

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

Fields of papers citing papers by Tommaso Marcelli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tommaso Marcelli

This figure shows the co-authorship network connecting the top 25 collaborators of Tommaso Marcelli. A scholar is included among the top collaborators of Tommaso Marcelli 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 Tommaso Marcelli. Tommaso Marcelli 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.
Liao, Rong‐Zhen, et al.. (2016). Origins of Stereoselectivity in Peptide-Catalyzed Kinetic Resolution of Alcohols. ACS Catalysis. 6(2). 1165–1171. 21 indexed citations
2.
Yuan, Bo, Tommaso Marcelli, Simon C. Willies, et al.. (2014). Enzymatic Desymmetrising Redox Reactions for the Asymmetric Synthesis of Biaryl Atropisomers. Chemistry - A European Journal. 20(41). 13084–13088. 53 indexed citations
3.
Byrne, Liam, Jordi Solà, Thomas Boddaert, et al.. (2013). Foldamer‐Mediated Remote Stereocontrol: >1,60 Asymmetric Induction. Angewandte Chemie International Edition. 53(1). 151–155. 105 indexed citations
4.
Volonterio, Alessandro, et al.. (2013). Multicomponent Synthesis of N-Carbamoyl Hydantoin Derivatives. Synlett. 24(6). 727–732. 6 indexed citations
5.
Brown, Robert A., Tommaso Marcelli, Matteo De Poli, Jordi Solà, & Jonathan Clayden. (2012). Induction of Unexpected Left‐Handed Helicity by an N‐Terminal L‐Amino Acid in an Otherwise Achiral Peptide Chain. Angewandte Chemie International Edition. 51(6). 1395–1399. 80 indexed citations
6.
Marcelli, Tommaso & Henk Hiemstra. (2012). Cinchona Alkaloids in Asymmetric Organocatalysis. Synthesis. 44(13). 2114–2114. 5 indexed citations
7.
Coppo, Paolo & Tommaso Marcelli. (2012). On the emission of bis-arylacetylide trinuclear Cu(I) complexes. Journal of Organometallic Chemistry. 710. 86–89. 5 indexed citations
8.
Bellucci, Maria Cristina, et al.. (2012). Regioselective multicomponent sequential synthesis of hydantoins. Organic & Biomolecular Chemistry. 10(48). 9538–9538. 22 indexed citations
9.
Marcelli, Tommaso, et al.. (2011). Domino synthesis of 1,3,5-trisubstituted hydantoins: a DFT study. Organic & Biomolecular Chemistry. 9(14). 5156–5156. 21 indexed citations
10.
Marcelli, Tommaso. (2011). Organocatalysis: Cinchona catalysts. Wiley Interdisciplinary Reviews Computational Molecular Science. 1(1). 142–152. 39 indexed citations
11.
Marcelli, Tommaso. (2010). Mechanistic Insights into Direct Amide Bond Formation Catalyzed by Boronic Acids: Halogens as Lewis Bases. Angewandte Chemie. 122(38). 6992–6995. 22 indexed citations
12.
Marcelli, Tommaso. (2010). Mechanistic Insights into Direct Amide Bond Formation Catalyzed by Boronic Acids: Halogens as Lewis Bases. Angewandte Chemie International Edition. 49(38). 6840–6843. 103 indexed citations
13.
Marcelli, Tommaso, Peter Hammar, & Fahmi Himo. (2008). Phosphoric Acid Catalyzed Enantioselective Transfer Hydrogenation of Imines: A Density Functional Theory Study of Reaction Mechanism and the Origins of Enantioselectivity. Chemistry - A European Journal. 14(28). 8562–8571. 136 indexed citations
14.
Marcelli, Tommaso, et al.. (2007). Construction of Adjacent Quaternary and Tertiary Stereocenters via an Organocatalytic Allylic Alkylation of Morita–Baylis–Hillman Carbonates. Advanced Synthesis & Catalysis. 349(3). 281–286. 132 indexed citations
15.
Hammar, Peter, Tommaso Marcelli, Henk Hiemstra, & Fahmi Himo. (2007). Density Functional Theory Study of the Cinchona Thiourea‐ Catalyzed Henry Reaction: Mechanism and Enantioselectivity. Advanced Synthesis & Catalysis. 349(17-18). 2537–2548. 86 indexed citations
16.
Marcelli, Tommaso, Richard N. S. van der Haas, Jan H. van Maarseveen, & Henk Hiemstra. (2006). Asymmetric Organocatalytic Henry Reaction. Angewandte Chemie International Edition. 45(6). 929–931. 282 indexed citations
17.
Marcelli, Tommaso, Jan H. van Maarseveen, & Henk Hiemstra. (2006). Cupreines and Cupreidines: An Emerging Class of Bifunctional Cinchona Organocatalysts. Angewandte Chemie International Edition. 45(45). 7496–7504. 316 indexed citations
18.
Marcelli, Tommaso, Richard N. S. van der Haas, Jan H. van Maarseveen, & Henk Hiemstra. (2006). Cinchona Derivatives as Bifunctional Organocatalysts for the Direct Asymmetric Nitroaldol (Henry) Reaction.. ChemInform. 37(14). 3 indexed citations
19.
Marcelli, Tommaso, Jan H. van Maarseveen, & Henk Hiemstra. (2006). Cupreine und Cupreidine: eine außergewöhnliche Klasse von bifunktionalen Cinchona‐Organokatalysatoren. Angewandte Chemie. 118(45). 7658–7666. 119 indexed citations
20.
Hiemstra, Henk, et al.. (2005). Cinchona Derivatives as Bifunctional Organocatalysts for the Direct Asymmetric Nitroaldol (Henry) Reaction. Synlett. 2817–2819. 4 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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