Franco Zarini

421 total citations
28 papers, 272 citations indexed

About

Franco Zarini is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, Franco Zarini has authored 28 papers receiving a total of 272 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Organic Chemistry, 10 papers in Molecular Biology and 7 papers in Pharmacology. Recurrent topics in Franco Zarini's work include Synthesis and Catalytic Reactions (6 papers), Synthesis and Reactions of Organic Compounds (6 papers) and Synthesis of β-Lactam Compounds (6 papers). Franco Zarini is often cited by papers focused on Synthesis and Catalytic Reactions (6 papers), Synthesis and Reactions of Organic Compounds (6 papers) and Synthesis of β-Lactam Compounds (6 papers). Franco Zarini collaborates with scholars based in Italy. Franco Zarini's co-authors include Angelo Bedeschi, Walter Cabri, Ilaria Candiani, Ettore Perrone, Marco Alpegiani, Giovanni Franceschi, Nicola Mongelli, Maria Chiara Fagnola, C Battistini and Federico Arcamone and has published in prestigious journals such as Journal of Antimicrobial Chemotherapy, Tetrahedron Letters and Pure and Applied Chemistry.

In The Last Decade

Franco Zarini

27 papers receiving 229 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Franco Zarini Italy 9 195 116 49 20 20 28 272
Ettore Perrone Italy 11 247 1.3× 123 1.1× 63 1.3× 29 1.4× 14 0.7× 58 352
M. ESSIZ France 9 210 1.1× 135 1.2× 74 1.5× 45 2.3× 30 1.5× 18 323
P. DI CESARE France 10 229 1.2× 142 1.2× 45 0.9× 12 0.6× 9 0.5× 21 298
William V. Curran United States 10 269 1.4× 148 1.3× 40 0.8× 8 0.4× 15 0.8× 34 359
Thomas W. Hudyma United States 10 170 0.9× 105 0.9× 63 1.3× 7 0.3× 7 0.3× 18 287
T. MIYAMOTO Japan 11 279 1.4× 174 1.5× 74 1.5× 33 1.6× 16 0.8× 21 390
C. L. Viswanathan India 10 265 1.4× 125 1.1× 19 0.4× 15 0.8× 25 1.3× 19 380
Sigmond G. Johnson United States 8 342 1.8× 164 1.4× 40 0.8× 20 1.0× 59 3.0× 10 471
Takenari Nakagome Japan 8 154 0.8× 82 0.7× 40 0.8× 26 1.3× 13 0.7× 39 228
Giovanni Franceschi Italy 11 304 1.6× 163 1.4× 93 1.9× 38 1.9× 14 0.7× 53 440

Countries citing papers authored by Franco Zarini

Since Specialization
Citations

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

Fields of papers citing papers by Franco Zarini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Franco Zarini

This figure shows the co-authorship network connecting the top 25 collaborators of Franco Zarini. A scholar is included among the top collaborators of Franco Zarini 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 Franco Zarini. Franco Zarini 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.
Fagnola, Maria Chiara, Ilaria Candiani, Walter Cabri, et al.. (1997). Solid-phase synthesis of indoles using the palladium-catalysed coupling of alkynes with iodoaniline derivatives. Tetrahedron Letters. 38(13). 2307–2310. 92 indexed citations
2.
Candiani, Ilaria, Angelo Bedeschi, Walter Cabri, et al.. (1997). Synthesis and cytotoxic activity of alkylidene- and alkyl-substituted camptothecins. Bioorganic & Medicinal Chemistry Letters. 7(7). 847–850. 2 indexed citations
3.
Bedeschi, Angelo, Franco Zarini, Walter Cabri, et al.. (1996). Synthesis and antitumor activity of a new class of water soluble camptothecin derivatives. Bioorganic & Medicinal Chemistry Letters. 6(6). 671–674. 8 indexed citations
4.
Cabri, Walter, Ilaria Candiani, Franco Zarini, Sergio Penco, & Angelo Bedeschi. (1995). A new high yield semisynthetic approach to (20s)-9-NH2-camptothecin based on a sequence of palladium-catalysed reductions. Tetrahedron Letters. 36(50). 9197–9200. 11 indexed citations
5.
Candiani, Ilaria, Walter Cabri, Franco Zarini, Angelo Bedeschi, & Sergio Penco. (1995). The Ligand Effect in Copper(I)-Catalyzed Chemoselective Amide Carbamoylation in Cabergoline Synthesis. Synlett. 1995(6). 605–606. 4 indexed citations
6.
Cabri, Walter, Ilaria Candiani, Franco Zarini, & Angelo Bedeschi. (1994). Zinc halides-mediated nucleophilic attack of thioacid salts in non protic media. A key step in the total synthesis of penems. Tetrahedron Letters. 35(20). 3379–3382. 1 indexed citations
7.
Jabés, Daniela, Rosaria Rossi, Ettore Perrone, et al.. (1993). Activity of new penems against defined MRSA strains. Bioorganic & Medicinal Chemistry Letters. 3(11). 2165–2170. 4 indexed citations
8.
Alpegiani, Marco, Angelo Bedeschi, Franco Zarini, et al.. (1992). Synthesis and biologicalproperties of FCE 25199, a new oral penem.. The Journal of Antibiotics. 45(5). 797–801. 3 indexed citations
9.
Bedeschi, Angelo, et al.. (1990). Synthesis and structure-activity relations in the class of 2-(pyridyl)penems.. The Journal of Antibiotics. 43(3). 306–313. 1 indexed citations
10.
Franceschi, Giovanni, et al.. (1990). 2-(Heteroatom-substituted)methyl Penems. IV. Oxygen Derivatives. Heterocycles. 30(2). 799–799. 9 indexed citations
11.
Franceschi, Giovanni, et al.. (1990). Reactivity Parameters of the Metal Assisted 1,2-Cleavage of Penicillins. Heterocycles. 31(4). 617–617.
12.
FRANCESCHI, G., Ettore Perrone, Marco Alpegiani, et al.. (1989). Synthesis and antimicrobial spectrum of FCE 22101 and its orally available ester FCE 22891. Journal of Antimicrobial Chemotherapy. 23(suppl C). 1–6. 13 indexed citations
13.
Franceschi, Giovanni, Marco Alpegiani, Angelo Bedeschi, Ettore Perrone, & Franco Zarini. (1988). 2-(Heteroaroma-substituted)methyl Penems. III. Nitrogen Derivatives. Heterocycles. 27(6). 1329–1329. 5 indexed citations
14.
Perrone, Ettore, Marco Alpegiani, Angelo Bedeschi, et al.. (1987). Novel quaternary ammonium penems: The ((pyridinio)methyl)phenyl derivatives.. The Journal of Antibiotics. 40(11). 1636–1639. 4 indexed citations
15.
Franceschi, Giovanni, Marco Alpegiani, C Battistini, et al.. (1987). Penems: some recent advances. Pure and Applied Chemistry. 59(3). 467–474. 8 indexed citations
16.
Perrone, Ettore, Marco Alpegiani, Angelo Bedeschi, et al.. (1986). 2-(Quaternary ammonio)-methyl penems.. The Journal of Antibiotics. 39(9). 1351–1355. 2 indexed citations
17.
Perrone, Ettore, Marco Alpegiani, Angelo Bedeschi, Franco Zarini, & Giovanni Franceschi. (1985). 2-(Heteroatom-substituted)methyl Penems. I. Sulphur Derivatives. Heterocycles. 23(9). 2255–2255. 9 indexed citations
18.
Battistini, C, et al.. (1983). Synthesis of New Orally Absorbed Penem Esters, Structurally Related to Thienamycin and Cephamycins. Heterocycles. 20(8). 1491–1491. 7 indexed citations
19.
Franceschi, Giovanni, et al.. (1982). Synthesis of Optically Active 6-Hydroxyethyl Penems. Heterocycles. 19(3). 485–485. 4 indexed citations
20.
Sanfilippo, A, Daniela Jabés, Giovanni Franceschi, et al.. (1982). Biological activity of (5R,6S,8R)-6-.ALPHA.-hydroxyethyl-2-acetoxymethyl-2-penem-3-carboxylate.. The Journal of Antibiotics. 35(9). 1248–1251. 8 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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