P. SCHENONE
Impact in
- Organic Chemistry top 2%
- Synthesis and biological activity
- Synthesis and Reactions of Organic Compounds
- Synthesis of heterocyclic compounds
- Synthesis and Biological Evaluation
- Multicomponent Synthesis of Heterocycles
- Synthesis and Characterization of Heterocyclic Compounds
- Organic Chemistry Cycloaddition Reactions
- Toxicology top 5%
Papers in
-
- Synthesis and Reactions of Organic Compounds 66
- Synthesis of heterocyclic compounds 40
- Synthesis and biological activity 33
- Synthesis and Characterization of Heterocyclic Compounds 21
- Synthesis and Biological Evaluation 20
- Organic Chemistry Cycloaddition Reactions 19
- Synthesis and Reactivity of Sulfur-Containing Compounds 13
- Co-authors
- Luisa Mosti (56 shared papers)Giulia Menozzi (53 shared papers)A. BARGAGNA (31 shared papers)Gaetano Bignardi (10 shared papers)Francesco Bondavalli (38 shared papers)Angelo Ranise (32 shared papers)E Marmo (33 shared papers)Michele D’Amico (15 shared papers)
- Journals
- Journal of the Chemical Society Perkin Transactions 1 (7 papers)Journal of Heterocyclic Chemistry (46 papers)International Journal of Cosmetic Science (2 papers)European Journal of Medicinal Chemistry (2 papers)Synthesis (1 paper)
- Partner nations
- ItalySwitzerlandAustralia
In The Last Decade
P. SCHENONE
120 papers receiving 890 citations
Peers
Comparison fields: 5 of 76
- Organic Chemistry 795
- Toxicology 39
- Pharmacology 125
- Pharmaceutical Science 35
- Molecular Biology 211
Countries citing papers authored by P. SCHENONE
This map shows the geographic impact of P. SCHENONE'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 P. SCHENONE with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites P. SCHENONE more than expected).
Fields of papers citing papers by P. SCHENONE
This network shows the impact of papers produced by P. SCHENONE. 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 P. SCHENONE. The network helps show where P. SCHENONE may publish in the future.
Co-authors
The 25 scholars most cited alongside P. SCHENONE, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 132 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1982 | 74 | |
| 2 | 1987 | 53 | |
| 3 | 1973 | 44 | |
| 4 | 1990 | 34 | |
| 5 | 3,5-diphenyl-1H-pyrazole derivatives. XI. N-aryl-5(3)-phenyl-4-(3,5- diphenyl-1-pyrazolyl)-3(5)-pyrazole amines, 5-substituted 4,5-dihydro-3-phenyl-4-(3,5-diphenyl-1-pyrazolyl)-1H-pyrazoles and 2,6-disubstituted 1,6-dihydro-4- phenyl-5-(3,5-diphenyl-1-pyrazolyl)pyrimidines with antipyretic, antiinflammatory and other activities. | 1993 | 32 |
| 6 | 1989 | 32 | |
| 7 | 1972 | 31 | |
| 8 | 3,5-Diphenyl-1H-pyrazole derivatives. V--1-Acetyl-4-hydroxy-3,5-diphenyl-2-pyrazoline esters, 4-hydroxy-3,5-diphenyl-1H-pyrazole esters and N-substituted 4-(3-amino-2-hydroxy-1-propoxy)-1-methyl-3,5-diphenyl-1H-pyrazoles with antiarrhythmic, sedative and platelet antiaggregating activities. | 1990 | 28 |
| 9 | 2H-[1]benzothiepino [5,4-b]pyran derivatives with local anesthetic and antiarrhythmic activities. | 1990 | 28 |
| 10 | 1993 | 27 | |
| 11 | 4-substituted 1-methyl-1H-indazoles with analgesic, antiinflammatory and antipyretic activities. | 1992 | 24 |
| 12 | 1985 | 23 | |
| 13 | 1983 | 20 | |
| 14 | 1972 | 20 | |
| 15 | 1-phenyl-1H-pyrazole derivatives with antiinflammatory, analgesic and antipiretic activities. | 1990 | 19 |
| 16 | 1983 | 17 | |
| 17 | 1979 | 16 | |
| 18 | Synthesis and cardiotonic activity of 2-substituted 5-cyano-1,6-dihydro-6-oxo-3-pyridinecarboxylic acids and their methyl or ethyl esters. | 1992 | 16 |
| 19 | 2H,5H-[1]benzothiopyrano [4,3-b]pyran derivatives with platelet antiaggregating activity. | 1990 | 13 |
| 20 | 1979 | 12 |
About P. SCHENONE
P. SCHENONE is a scholar working on Organic Chemistry, Molecular Biology, Pharmacology, Spectroscopy and Pharmaceutical Science, having authored 132 papers that have together received 951 indexed citations. Recurring topics across this work include Synthesis and Reactions of Organic Compounds (66 papers), Synthesis of heterocyclic compounds (40 papers), Synthesis and biological activity (33 papers), Synthesis and Characterization of Heterocyclic Compounds (21 papers), Synthesis and Biological Evaluation (20 papers), Organic Chemistry Cycloaddition Reactions (19 papers), Synthesis of Organic Compounds (15 papers) and Synthesis and Reactivity of Sulfur-Containing Compounds (13 papers). The work is most often cited by research in Organic Chemistry (795 citations), Toxicology (39 citations), Pharmacology (125 citations), Pharmaceutical Science (35 citations) and Molecular Biology (211 citations). P. SCHENONE has collaborated with scholars based in Italy, Switzerland and Australia. Frequent co-authors include Luisa Mosti, Giulia Menozzi, A. BARGAGNA, Gaetano Bignardi, Francesco Bondavalli, Angelo Ranise, E Marmo, Michele D’Amico, Olga Bruno and Filippo Evangelisti. Their work appears in journals such as Journal of the Chemical Society Perkin Transactions 1, Journal of Heterocyclic Chemistry, International Journal of Cosmetic Science, European Journal of Medicinal Chemistry and Synthesis.
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.