Fiorenza Viani

1.6k total citations
96 papers, 1.3k citations indexed

About

Fiorenza Viani is a scholar working on Organic Chemistry, Pharmaceutical Science and Molecular Biology. According to data from OpenAlex, Fiorenza Viani has authored 96 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 61 papers in Organic Chemistry, 52 papers in Pharmaceutical Science and 33 papers in Molecular Biology. Recurrent topics in Fiorenza Viani's work include Fluorine in Organic Chemistry (52 papers), Carbohydrate Chemistry and Synthesis (17 papers) and Chemical Synthesis and Analysis (17 papers). Fiorenza Viani is often cited by papers focused on Fluorine in Organic Chemistry (52 papers), Carbohydrate Chemistry and Synthesis (17 papers) and Chemical Synthesis and Analysis (17 papers). Fiorenza Viani collaborates with scholars based in Italy, Japan and Ukraine. Fiorenza Viani's co-authors include Pierfrancesco Bravo, Matteo Zanda, Cristina Pesenti, Vadim A. Soloshonok, Massimo Frigerio, Stefano V. Meille, Alberto Arnone, Alessandra Farina, Giuseppe Resnati and Walter Panzeri and has published in prestigious journals such as Biochemical and Biophysical Research Communications, Journal of Medicinal Chemistry and The Journal of Organic Chemistry.

In The Last Decade

Fiorenza Viani

90 papers receiving 1.3k citations

Peers

Fiorenza Viani
Luke Hunter Australia
Bruno Bernet Switzerland
Richard D. Tillyer United States
A. M. VAN LEUSEN Netherlands
David C. Blakemore United Kingdom
Luke Hunter Australia
Fiorenza Viani
Citations per year, relative to Fiorenza Viani Fiorenza Viani (= 1×) peers Luke Hunter

Countries citing papers authored by Fiorenza Viani

Since Specialization
Citations

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

Fields of papers citing papers by Fiorenza Viani

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fiorenza Viani

This figure shows the co-authorship network connecting the top 25 collaborators of Fiorenza Viani. A scholar is included among the top collaborators of Fiorenza Viani 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 Fiorenza Viani. Fiorenza Viani 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.
Pizzi, Andrea, et al.. (2023). Chalcogen Bonding (ChB) as a Robust Supramolecular Recognition Motif of Benzisothiazolinone Antibacterials. Chemistry - A European Journal. 29(32). e202300571–e202300571. 8 indexed citations
2.
Bellucci, Maria Cristina, Carlo Castellano, Fiorella Meneghetti, et al.. (2022). Synthesis and Conformational Analysis of Hydantoin-Based Universal Peptidomimetics. The Journal of Organic Chemistry. 88(15). 10381–10402. 7 indexed citations
3.
Bono, Nina, Federica Ponti, Maria Cristina Bellucci, et al.. (2021). Multifunctional Neomycin-Triazine-Based Cationic Lipids for Gene Delivery with Antibacterial Properties. Bioconjugate Chemistry. 32(4). 690–701. 11 indexed citations
4.
Falconi, Mattia, Sarah Ciccone, Paola D’Arrigo, et al.. (2013). Design of a novel LOX-1 receptor antagonist mimicking the natural substrate. Biochemical and Biophysical Research Communications. 438(2). 340–345. 31 indexed citations
5.
D’Arrigo, Paola, et al.. (2011). Overexpression of a bacterial chymotrypsin: Application for l-amino acid ester hydrolysis. Enzyme and Microbial Technology. 49(6-7). 560–566. 1 indexed citations
6.
Candiani, Gabriele, Fiorenza Viani, Chiara Verpelli, et al.. (2006). Dimerizable Redox‐Sensitive Triazine‐Based Cationic Lipids for in vitro Gene Delivery. ChemMedChem. 2(3). 292–296. 36 indexed citations
7.
Sani, Monica, et al.. (2006). Peptidyl Fluoro-Ketones as Proteolytic Enzyme Inhibitors. Current Topics in Medicinal Chemistry. 6(14). 1545–1566. 11 indexed citations
8.
Binkert, Christoph A., Andrew F. Jones, Solange Meyer, et al.. (2005). Replacement of Isobutyl by Trifluoromethyl in Pepstatin A Selectively Affects Inhibition of Aspartic Proteinases. ChemBioChem. 7(1). 181–186. 30 indexed citations
9.
Bravo, Pierfrancesco, Silvia C. Capelli, Marcello Crucianelli, et al.. (1999). Asymmetric synthesis of α-arylglycinols via additions of lithium methyl p-tolyl sulfoxide to N-(PMP)arylaldimines followed by “non oxidative” Pummerer reaction. Tetrahedron. 55(10). 3025–3040. 46 indexed citations
10.
Arnone, Alberto, Pierfrancesco Bravo, Massimo Frigerio, et al.. (1999). Synthesis of Enantiomerically Pure 2′,3′,5′-Trideoxy-4′-[(diethoxyphosphoryl)difluoromethyl]thymidine Analogues. European Journal of Organic Chemistry. 1999(9). 2149–2157. 7 indexed citations
11.
Arnone, Alberto, et al.. (1998). Synthesis of 3′-Arylsulfonyl-4′-[(diethoxyphosphoryl)difluoromethyl]thymidine. Synthesis. 1998(10). 1511–1518. 7 indexed citations
12.
Bravo, Pierfrancesco, Fiorenza Viani, Donata Favretto, & Pietro Traldi. (1996). Fast-atom Bombardment Mass Spectrometry of Some Nucleoside Analogs. Rapid Communications in Mass Spectrometry. 10(9). 1103–1106. 3 indexed citations
13.
Mele, Andrea, et al.. (1995). Synthesis of 4'-Fluoroalkyl Nucleoside Analogues. Gazzetta chimica italiana. 125. 295–303. 4 indexed citations
14.
Arnone, Alberto, Pierfrancesco Bravo, Massimo Frigerio, et al.. (1994). On the synthesis of optically pure monofluorocyclohexanol derivatives by the fluorinated sulfoxide chiron route. Tetrahedron. 50(43). 12361–12374. 6 indexed citations
15.
Arnone, Alberto, et al.. (1994). Synthetically useful C-4 fluorinated building blocks bearing a quaternary stereocentre. Tetrahedron. 50(47). 13485–13492. 12 indexed citations
16.
Bravo, Pierfrancesco, Massimo Frigerio, Giovanni Fronza, et al.. (1994). Stereoselective oxirane formation by reaction of diazomethane on 1-fluoro-3-[(4-methylphenyl)sulfinyl]-3-phenylpropan-2-one. Canadian Journal of Chemistry. 72(8). 1769–1779. 9 indexed citations
17.
Bravo, Pierfrancesco, Giuseppe Resnati, Piero Angeli, et al.. (1992). Synthesis and pharmacological evaluation of enantiomerically pure 4-deoxy-4-fluoromuscarines. Journal of Medicinal Chemistry. 35(17). 3102–3110. 35 indexed citations
18.
Frigerio, Mark, et al.. (1990). Total synthesis of homochiral 3-deoxy-3-fluoromuscarines.. Gazzetta chimica italiana. 120(4). 275–276. 11 indexed citations
19.
Bravo, Pierfrancesco, Giuseppe Resnati, & Fiorenza Viani. (1989). Synthesis of fluorinated analogues of acyclic nucleosides as potential antiviral agents. Journal of Fluorine Chemistry. 45(1). 119–119. 2 indexed citations
20.
Resnati, Giuseppe, et al.. (1986). A selective method for 3-monoalkylation of 4-hydroxypyran-2-ones and of 4-hydroxyquinolin-2(1H)-ones or their N-methyl derivatives by ketone Mannich bases. Journal of Chemical Research Synopses. 374–375.

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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