Giada Moscatelli

444 total citations
12 papers, 387 citations indexed

About

Giada Moscatelli is a scholar working on Organic Chemistry, Pharmaceutical Science and Molecular Biology. According to data from OpenAlex, Giada Moscatelli has authored 12 papers receiving a total of 387 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Organic Chemistry, 3 papers in Pharmaceutical Science and 1 paper in Molecular Biology. Recurrent topics in Giada Moscatelli's work include Cyclopropane Reaction Mechanisms (8 papers), Click Chemistry and Applications (4 papers) and Synthesis and Biological Evaluation (4 papers). Giada Moscatelli is often cited by papers focused on Cyclopropane Reaction Mechanisms (8 papers), Click Chemistry and Applications (4 papers) and Synthesis and Biological Evaluation (4 papers). Giada Moscatelli collaborates with scholars based in Italy and Greece. Giada Moscatelli's co-authors include Gianfranco Favi, Orazio A. Attanasi, Fabio Mantellini, Paolino Fïlippone, Stefania Santeusanio, Gianluca Giorgi, Francesca R. Perrulli, Lucia De Crescentini, Mohamed S. Behalo and Athina Geronikaki and has published in prestigious journals such as The Journal of Organic Chemistry, Organic Letters and Advanced Synthesis & Catalysis.

In The Last Decade

Giada Moscatelli

12 papers receiving 381 citations

Peers

Giada Moscatelli
Giada Moscatelli
Citations per year, relative to Giada Moscatelli Giada Moscatelli (= 1×) peers Kenji Azechi

Countries citing papers authored by Giada Moscatelli

Since Specialization
Citations

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

Fields of papers citing papers by Giada Moscatelli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Giada Moscatelli

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

All Works

12 of 12 papers shown
4.
Attanasi, Orazio A., Gianfranco Favi, Gianluca Giorgi, et al.. (2013). Synthesis of Tetrahydropyridazine Amino Acid Derivatives by a Formal [4+2] Cycloaddition Reaction of 1,2-Diaza-1,3-dienes with Dehydroalanine Esters.. Current Organic Synthesis. 10(5). 803–811. 4 indexed citations
5.
Attanasi, Orazio A., Stefano Menichetti, Gianfranco Favi, et al.. (2012). Synthesis of Highly Functionalized 1,3-Oxathioles via an Unusual [4+1] Annulation of α,α'-Dioxothione with 1,2-Diaza-1,3-dienes. Synlett. 23(20). 2947–2950. 5 indexed citations
6.
Attanasi, Orazio A., Gianfranco Favi, Fabio Mantellini, Giada Moscatelli, & Stefania Santeusanio. (2011). A Novel Assembly of Substituted Pyrroles by Acid‐Catalyzed Sequential Three‐Component Reaction of Amines, Alkynoates, and 1,2‐Diaza‐1,3‐dienes. Advanced Synthesis & Catalysis. 353(9). 1519–1524. 32 indexed citations
7.
Attanasi, Orazio A., Gianfranco Favi, Fabio Mantellini, Giada Moscatelli, & Stefania Santeusanio. (2011). Synthesis of Functionalized Pyrroles via Catalyst- and Solvent-Free Sequential Three-Component Enamine−Azoene Annulation. The Journal of Organic Chemistry. 76(8). 2860–2866. 68 indexed citations
8.
Attanasi, Orazio A., Gianfranco Favi, Paolino Fïlippone, et al.. (2009). Copper(II)/Copper(I)-Catalyzed Aza-Michael Addition/Click Reaction of in Situ Generated α-Azidohydrazones: Synthesis of Novel Pyrazolone−Triazole Framework. Organic Letters. 12(3). 468–471. 59 indexed citations
9.
Attanasi, Orazio A., Lucia De Crescentini, Gianfranco Favi, et al.. (2009). An Efficient One-Pot, Three-Component Synthesis of 5-Hydrazinoalkylidene Rhodanines from 1,2-Diaza-1,3-dienes. Organic Letters. 11(11). 2265–2268. 58 indexed citations
10.
Attanasi, Orazio A., Gianfranco Favi, Paolino Fïlippone, et al.. (2008). Flexible Protocol for the Chemo- and Regioselective Building of Pyrroles and Pyrazoles by Reactions of Danishefsky’s Dienes with 1,2-Diaza-1,3-butadienes. Organic Letters. 10(10). 1983–1986. 35 indexed citations
11.
Attanasi, Orazio A., Paolo Davoli, Gianfranco Favi, et al.. (2007). Azavinyl Azomethine Ylides from Thermal Ring Opening of α-Aziridinohydrazones:  Unprecedented 1,5-Electrocyclization to Imidazoles. Organic Letters. 9(17). 3461–3464. 30 indexed citations
12.
Attanasi, Orazio A., Gianfranco Favi, Paolino Fïlippone, et al.. (2006). Tetrabromo Hydrogenated Cardanol:  Efficient and Renewable Brominating Agent. Organic Letters. 8(19). 4291–4293. 38 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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