Lucio Pellacani

1.6k total citations
97 papers, 1.2k citations indexed

About

Lucio Pellacani is a scholar working on Organic Chemistry, Molecular Biology and Pharmaceutical Science. According to data from OpenAlex, Lucio Pellacani has authored 97 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 89 papers in Organic Chemistry, 29 papers in Molecular Biology and 22 papers in Pharmaceutical Science. Recurrent topics in Lucio Pellacani's work include Synthesis and Catalytic Reactions (54 papers), Chemical Synthesis and Analysis (22 papers) and Fluorine in Organic Chemistry (21 papers). Lucio Pellacani is often cited by papers focused on Synthesis and Catalytic Reactions (54 papers), Chemical Synthesis and Analysis (22 papers) and Fluorine in Organic Chemistry (21 papers). Lucio Pellacani collaborates with scholars based in Italy, New Zealand and Spain. Lucio Pellacani's co-authors include Paolo A. Tardella, Stefania Fioravanti, M. Antonietta Loreto, Fabio Sciubba, Sergio Lociuro, Roberto Ballini, Alessandro Canella, Paola Bergamini, R. Berni and Riccardo Gavioli and has published in prestigious journals such as Journal of Molecular Biology, Inorganic Chemistry and The Journal of Organic Chemistry.

In The Last Decade

Lucio Pellacani

94 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lucio Pellacani Italy 19 1.1k 273 222 115 63 97 1.2k
Paolo A. Tardella Italy 19 1.1k 1.0× 248 0.9× 144 0.6× 103 0.9× 12 0.2× 95 1.2k
Daniel Zimmerli Switzerland 10 580 0.5× 275 1.0× 474 2.1× 146 1.3× 39 0.6× 17 883
Saverio Florio Italy 26 2.0k 1.8× 370 1.4× 111 0.5× 261 2.3× 49 0.8× 136 2.2k
Stefania Fioravanti Italy 19 941 0.8× 241 0.9× 274 1.2× 116 1.0× 10 0.2× 78 1.1k
François Trécourt France 27 1.5k 1.3× 242 0.9× 111 0.5× 228 2.0× 24 0.4× 52 1.7k
Johannes A. Burkhard Switzerland 13 998 0.9× 354 1.3× 145 0.7× 102 0.9× 16 0.3× 17 1.2k
Matthew Brichacek United States 11 1.2k 1.0× 284 1.0× 142 0.6× 222 1.9× 71 1.1× 20 1.4k
А. Г. Ибрагимов Russia 19 1.5k 1.4× 306 1.1× 86 0.4× 315 2.7× 45 0.7× 220 1.6k
U. K. PANDIT Netherlands 18 761 0.7× 414 1.5× 82 0.4× 72 0.6× 43 0.7× 111 1.1k
Etsuji Okada Japan 17 811 0.7× 158 0.6× 447 2.0× 54 0.5× 19 0.3× 94 901

Countries citing papers authored by Lucio Pellacani

Since Specialization
Citations

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

Fields of papers citing papers by Lucio Pellacani

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lucio Pellacani

This figure shows the co-authorship network connecting the top 25 collaborators of Lucio Pellacani. A scholar is included among the top collaborators of Lucio Pellacani 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 Lucio Pellacani. Lucio Pellacani 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.
2.
Fioravanti, Stefania, et al.. (2015). Trifluoromethyl syn- or anti-γ-amino alcohols by one-pot solvent-free Mannich-type reactions under temperature control. RSC Advances. 5(37). 29312–29318. 7 indexed citations
3.
Fioravanti, Stefania, et al.. (2015). New Synthesis of Trifluoromethyl Aldimines Containing L‐α‐Amino Ester Moieties and Their Use in Mannich‐Type Reactions. Chirality. 27(9). 571–575. 8 indexed citations
4.
Fioravanti, Stefania, et al.. (2014). Trifluoromethyl-modified dipeptides by ZrCl4-promoted aza-Henry reactions. Amino Acids. 46(8). 1961–1970. 16 indexed citations
5.
Fioravanti, Stefania, et al.. (2013). Selective Amination Reactions of α-Nitro Aryl and Heteroaryl Enoates. The Journal of Organic Chemistry. 78(16). 8203–8207. 10 indexed citations
6.
Fioravanti, Stefania, et al.. (2013). Desymmetrization of α-diimines: synthesis of new 3-(diaziridin-3-yl)oxaziridines. Tetrahedron Letters. 54(34). 4574–4576. 3 indexed citations
7.
Fioravanti, Stefania, et al.. (2012). Fluorinated β-nitro amines by a selective ZrCl4-catalyzed aza-Henry reaction of (E)-trifluoromethyl aldimines. Organic & Biomolecular Chemistry. 10(41). 8207–8207. 19 indexed citations
8.
Fioravanti, Stefania, et al.. (2011). Domino reactions for the synthesis of various α-substituted nitro alkenes. Organic & Biomolecular Chemistry. 10(3). 524–528. 21 indexed citations
9.
Fioravanti, Stefania, et al.. (2008). Solution-phase synthesis of 2-cyano and 2-amido aziridinyl peptides. Tetrahedron. 64(14). 3204–3211. 12 indexed citations
10.
Fioravanti, Stefania, et al.. (2008). Stereoselective aza-MIRC reactions on optically active (E)-nitro alkenes. Tetrahedron Asymmetry. 19(2). 231–236. 22 indexed citations
11.
Fioravanti, Stefania, et al.. (2005). Can functionalized N-acyloxy aziridines be easily deprotected?. Comptes Rendus Chimie. 8(5). 845–847. 6 indexed citations
12.
Fioravanti, Stefania, et al.. (2003). Functionalised enones as starting materials for the construction of aziridine scaffolds. Molecular Diversity. 6(3-4). 177–180. 3 indexed citations
13.
Fioravanti, Stefania, et al.. (2002). Diastereoselective Aziridination of Chiral α-Carbonyl Enoates1. The Journal of Organic Chemistry. 67(14). 4972–4974. 21 indexed citations
14.
Fioravanti, Stefania, et al.. (2001). Direct amination of β-oxo esters. Tetrahedron Letters. 42(6). 1171–1173. 15 indexed citations
15.
Santis, Marco De, Stefania Fioravanti, Lucio Pellacani, & Paolo A. Tardella. (1999). Optically Pure 3,6-Dioxazocan-2-one Derivatives by Intramolecular Cycloaddition of Azidoformates and their Opening to Substituted α-Amino Ketones. European Journal of Organic Chemistry. 1999(11). 2709–2711. 2 indexed citations
16.
Fioravanti, Stefania, M. Antonietta Loreto, Lucio Pellacani, & Paolo A. Tardella. (1990). Asymmetric addition of ethyl azidoformate to optically active enamines. Reversal of facial selectivity compared with (ethoxycarbonyl)nitrene. Tetrahedron Asymmetry. 1(12). 931–936. 18 indexed citations
17.
Loreto, M. Antonietta, et al.. (1985). Reaction of 2,2-dichlorocyclobutanones with pyridinium chloride.. Journal of Chemical Research Synopses. 158–159.
18.
Pellacani, Lucio, et al.. (1979). Regioselectivity of the (ethoxycarbonyl)nitrene insertion reaction on monochloro- and dichloroalkanes and cycloalkanes. The Journal of Organic Chemistry. 44(21). 3605–3607. 4 indexed citations
19.
Loreto, M. Antonietta, Lucio Pellacani, & Paolo A. Tardella. (1979). Synthesis of N‐ethoxycarbonyl‐7‐azabicyclo[4.2.1]nonane and N‐ethoxycarbonyl‐9‐azabicyclo[4.2.1]nonane. Journal of Heterocyclic Chemistry. 16(6). 1233–1234. 4 indexed citations
20.
Tardella, Paolo A. & Lucio Pellacani. (1975). Synthesis and reductive ring cleavage of N‐carbethoxy‐8‐azatricyclo[4.3.0.07,9]nonane. Journal of Heterocyclic Chemistry. 12(2). 449–450. 2 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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