Gianluca Papeo

1.2k total citations
34 papers, 858 citations indexed

About

Gianluca Papeo is a scholar working on Organic Chemistry, Molecular Biology and Oncology. According to data from OpenAlex, Gianluca Papeo has authored 34 papers receiving a total of 858 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Organic Chemistry, 16 papers in Molecular Biology and 7 papers in Oncology. Recurrent topics in Gianluca Papeo's work include Chemical Synthesis and Analysis (7 papers), PARP inhibition in cancer therapy (6 papers) and Synthetic Organic Chemistry Methods (5 papers). Gianluca Papeo is often cited by papers focused on Chemical Synthesis and Analysis (7 papers), PARP inhibition in cancer therapy (6 papers) and Synthetic Organic Chemistry Methods (5 papers). Gianluca Papeo collaborates with scholars based in Italy, Canada and Switzerland. Gianluca Papeo's co-authors include Francesca Quartieri, Alessandra Scolaro, Beatrice Malgesini, Barbara Forte, Claudia Piutti, Daniela Borghi, Massimo Sisti, Rita Annunziata, Helena Posteri and Giovanni Palmisano and has published in prestigious journals such as Journal of the American Chemical Society, Cancer Research and The Journal of Organic Chemistry.

In The Last Decade

Gianluca Papeo

33 papers receiving 830 citations

Peers

Gianluca Papeo
Pierre J. De Clercq Belgium
Kristopher M. Depew United States
Kabirul Islam United States
Ange Pancrazi France
Dennis X. Hu United States
Shyam Krishnan United States
F. GUIBE France
Ravi S. Garigipati United States
Chad Bennett United States
Valeria Di Bussolo Italy
Pierre J. De Clercq Belgium
Gianluca Papeo
Citations per year, relative to Gianluca Papeo Gianluca Papeo (= 1×) peers Pierre J. De Clercq

Countries citing papers authored by Gianluca Papeo

Since Specialization
Citations

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

Fields of papers citing papers by Gianluca Papeo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gianluca Papeo

This figure shows the co-authorship network connecting the top 25 collaborators of Gianluca Papeo. A scholar is included among the top collaborators of Gianluca Papeo 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 Gianluca Papeo. Gianluca Papeo 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.
Casuscelli, Francesco, Elena Ardini, Nilla Avanzi, et al.. (2022). Stereoselective synthesis of 3,4‐dihydropyrrolo[1,2‐a]pyrazin‐1(2H)‐one derivatives as PIM kinase inhibitors inspired from marine alkaloids. Chirality. 34(11). 1437–1452. 3 indexed citations
2.
3.
Montagnoli, Alessia, Sonia Rainoldi, Antonella Ciavolella, et al.. (2016). Abstract 1223: NMS-P293, a novel potent and selective PARP-1 inhibitor with high antitumor efficacy and tolerability. Cancer Research. 76(14_Supplement). 1223–1223. 4 indexed citations
4.
Papeo, Gianluca, Nilla Avanzi, Serena Bettoni, et al.. (2014). Insights into PARP Inhibitors’ Selectivity Using Fluorescence Polarization and Surface Plasmon Resonance Binding Assays. SLAS DISCOVERY. 19(8). 1212–1219. 18 indexed citations
5.
Papeo, Gianluca, Elena Casale, Alessia Montagnoli, & Alessandra Cirla. (2013). PARP inhibitors in cancer therapy: an update. Expert Opinion on Therapeutic Patents. 23(4). 503–514. 39 indexed citations
6.
Casuscelli, Francesco, Elena Ardini, Nilla Avanzi, et al.. (2013). Discovery and optimization of pyrrolo[1,2-a]pyrazinones leads to novel and selective inhibitors of PIM kinases. Bioorganic & Medicinal Chemistry. 21(23). 7364–7380. 28 indexed citations
7.
Papeo, Gianluca & Maurizio Pulici. (2013). Italian Chemists’ Contributions to Named Reactions in Organic Synthesis: An Historical Perspective. Molecules. 18(9). 10870–10900. 16 indexed citations
8.
Quartieri, Francesca, et al.. (2011). Total Synthesis of (+)‐7,11‐Helianane and (+)‐5‐Chloro‐7,11‐helianane through Stereoselective Aromatic Claisen Rearrangement. European Journal of Organic Chemistry. 2011(33). 6802–6802. 1 indexed citations
9.
Malgesini, Beatrice, Barbara Forte, Daniela Borghi, et al.. (2009). A Straightforward Total Synthesis of (−)‐Chaetominine. Chemistry - A European Journal. 15(32). 7922–7929. 43 indexed citations
10.
Papeo, Gianluca, Barbara Forte, Paolo Orsini, et al.. (2009). Poly(ADP-ribose) polymerase inhibition in cancer therapy: are we close to maturity?. Expert Opinion on Therapeutic Patents. 19(10). 1377–1400. 34 indexed citations
11.
Forte, Barbara, Beatrice Malgesini, Claudia Piutti, et al.. (2009). A Submarine Journey: The Pyrrole-Imidazole Alkaloids. Marine Drugs. 7(4). 705–753. 190 indexed citations
12.
Malgesini, Beatrice, Eduard Felder, Nicola Mongelli, & Gianluca Papeo. (2008). Improved synthesis of polyfluorinated l-lysine for 19F NMR-based screening. Molecular Diversity. 13(1). 53–56. 2 indexed citations
13.
Papeo, Gianluca, Patrizia Giordano, Maria Gabriella Brasca, et al.. (2007). Polyfluorinated Amino Acids for Sensitive 19F NMR-Based Screening and Kinetic Measurements. Journal of the American Chemical Society. 129(17). 5665–5672. 39 indexed citations
14.
Papeo, Gianluca, Helena Posteri, Daniela Borghi, & Mario Varasi. (2005). A New Glycociamidine Ring Precursor:  Syntheses of (Z)-Hymenialdisine, (Z)-2-Debromohymenialdisine, and (±)-endo-2-Debromohymenialdisine. Organic Letters. 7(25). 5641–5644. 37 indexed citations
15.
Papeo, Gianluca, Helena Posteri, Paola Vianello, & Mario Varasi. (2004). Nicotinoyl Azide (NCA)-Mediated Mitsunobu Reaction: An Expedient One-Pot Transformation of Alcohols into Azides. Synthesis. 2004(17). 2886–2892. 19 indexed citations
16.
Hanessian, Stephen, et al.. (2004). Synthesis of 310-Helix-Inducing Constrained Analogues of l-Proline. The Journal of Organic Chemistry. 69(15). 4891–4899. 26 indexed citations
17.
Forte, Barbara, et al.. (2003). Facile Synthesis of 7-Amino-1,2,3,4-tetrahydro-β-carboline. Synthetic Communications. 33(21). 3707–3716.
18.
Palmisano, Giovanni, Rita Annunziata, Gianluca Papeo, & Massimo Sisti. (1996). Oxindole alkaloids. A novel non-biomimetic entry to (−)-Horsfiline.. Tetrahedron Asymmetry. 7(1). 1–4. 88 indexed citations
19.
Colombo, Lino, Marcello Di Giacomo, Gianluca Papeo, et al.. (1994). Synthesis of 7,5-fused bicyclic lactams by stereoselective radical cyclization. Tetrahedron Letters. 35(23). 4031–4034. 20 indexed citations
20.
Giacomo, Marcello Di, et al.. (1993). Synthesis of a preclavulones analogous : (±) 8,12-trans-(5Z, 14Z)-9-oxo-prosta-5,10,14-trienoic acid methyl ester via its 10-11 dihydroprecursor from allyl 2-oxo-cyclopentanecarboxylate. Il Farmaco. 48(1). 117–126. 3 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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