Oreste Livi

1.5k total citations
119 papers, 1.2k citations indexed

About

Oreste Livi is a scholar working on Organic Chemistry, Molecular Biology and Physiology. According to data from OpenAlex, Oreste Livi has authored 119 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 98 papers in Organic Chemistry, 43 papers in Molecular Biology and 26 papers in Physiology. Recurrent topics in Oreste Livi's work include Synthesis and Characterization of Heterocyclic Compounds (48 papers), Synthesis and Biological Evaluation (44 papers) and Click Chemistry and Applications (38 papers). Oreste Livi is often cited by papers focused on Synthesis and Characterization of Heterocyclic Compounds (48 papers), Synthesis and Biological Evaluation (44 papers) and Click Chemistry and Applications (38 papers). Oreste Livi collaborates with scholars based in Italy and United States. Oreste Livi's co-authors include Irene Giorgi, Valerio Scartoni, Giuliana Biagi, G. BIAGI, Vincenzo Calderone, Enrica Martinotti, Antonio Lucacchini, P. L. BARILI, Alma Martelli and Laura Betti and has published in prestigious journals such as Journal of Medicinal Chemistry, Tetrahedron and Journal of Pharmaceutical Sciences.

In The Last Decade

Oreste Livi

116 papers receiving 1.2k citations

Peers

Oreste Livi
Harriet W. Hamilton United States
C. John Blankley United States
Simon D. Guile United Kingdom
Anthony K. L. Fung United States
John P. Caldwell United States
Oreste Livi
Citations per year, relative to Oreste Livi Oreste Livi (= 1×) peers Irene Giorgi

Countries citing papers authored by Oreste Livi

Since Specialization
Citations

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

Fields of papers citing papers by Oreste Livi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Oreste Livi

This figure shows the co-authorship network connecting the top 25 collaborators of Oreste Livi. A scholar is included among the top collaborators of Oreste Livi 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 Oreste Livi. Oreste Livi 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.
Coi, Alessio, et al.. (2008). QSAR studies on BK channel activators. Bioorganic & Medicinal Chemistry. 17(1). 319–325. 12 indexed citations
2.
Calderone, Vincenzo, et al.. (2007). New amido derivatives as potential BKCa potassium channel activators. XI. European Journal of Medicinal Chemistry. 43(4). 792–799. 2 indexed citations
3.
Giorgi, Irene, Giuliana Biagi, Anna Maria Bianucci, et al.. (2007). N6-1,3-Diphenylurea derivatives of 2-phenyl-9-benzyladenines and 8-azaadenines: Synthesis and biological evaluation as allosteric modulators of A2A adenosine receptors. European Journal of Medicinal Chemistry. 43(8). 1639–1647. 21 indexed citations
4.
Biagi, Giuliana, Anna Maria Bianucci, Alessio Coi, et al.. (2005). 2,9-Disubstituted-N6-(arylcarbamoyl)-8-azaadenines as new selective A3 adenosine receptor antagonists: Synthesis, biochemical and molecular modelling studies. Bioorganic & Medicinal Chemistry. 13(15). 4679–4693. 17 indexed citations
5.
Biagi, Giuliana, Irene Giorgi, Michele Leonardi, et al.. (2003). New N6- or N(9)-hydroxyalkyl substituted 8-azaadenines or adenines as effective A1 adenosine receptor ligands. European Journal of Medicinal Chemistry. 38(9). 801–810. 7 indexed citations
6.
Biagi, Giuliana, Irene Giorgi, Oreste Livi, et al.. (2003). N6-Cycloalkyl-2-phenyl-3-deaza-8-azaadenines: a new class of A1 adenosine receptor ligands. A comparison with the corresponding adenines and 8-azaadenines. European Journal of Medicinal Chemistry. 38(11-12). 983–990. 12 indexed citations
7.
Biagi, Giuliana, Irene Giorgi, Oreste Livi, et al.. (2001). New 5-substituted-1-(2-hydroxybenzoyl)-benzotriazoles, potassium channel activators. IV. Il Farmaco. 56(11). 827–834. 20 indexed citations
8.
Biagi, Giuliana, et al.. (2001). New 2-(2′-phenyl-9′-benzyl-8′-azapurin-6′-ylamino)-carboxylic acid methylesters as ligands for A1 adenosine receptors. Il Farmaco. 56(12). 929–931. 4 indexed citations
9.
Biagi, Giuliana, et al.. (2001). 2-Alkyloxyalkylthiohypoxanthines as new potent inhibitors of xanthine oxidase. Il Farmaco. 56(11). 809–813. 20 indexed citations
10.
Biagi, Giuliana, Vincenzo Calderone, Irene Giorgi, et al.. (2000). 5-(4′-Substituted-2′-nitroanilino)-1,2,3-triazoles as new potential potassium channel activators. I. European Journal of Medicinal Chemistry. 35(7-8). 715–720. 41 indexed citations
11.
Baragatti, Barbara, Giuliana Biagi, Vincenzo Calderone, et al.. (2000). Triazolyl–benzimidazolones and triazolyl–benzotriazoles: new potential potassium channel activators. II. European Journal of Medicinal Chemistry. 35(10). 949–955. 27 indexed citations
12.
BIAGI, G., Irene Giorgi, Clementina Manera, et al.. (1998). 1,2,3-トリアゾロ[1,5-a]キノキサリン類 合成ならびにベンゾジアゼピンおよびアデノシン受容器への結合性. 33(2). 113–122. 30 indexed citations
13.
BIAGI, G., et al.. (1996). 1,2,3-Triazolo[1,5-a][1,3]benzodiazepine a new heterocyclic system: Synthesis, benzodiazepine receptor binding and theoretical calculations. Il Farmaco. 51(1). 13–18. 8 indexed citations
14.
BIAGI, G., Irene Giorgi, Oreste Livi, & Valerio Scartoni. (1995). Synthesis of new 3-benzyl-5-phenyl-7-alkylaminothiazolo [4,5-d]pyrimidine-2(3H)-thiones. Il Farmaco. 50(9). 579–586. 1 indexed citations
15.
BIAGI, G., Irene Giorgi, Oreste Livi, et al.. (1994). N(6)-substituted 2-N-butyl-9-benzyl-8-azaadenines. Affinity for adenosine A1 and A2 receptors. IV.. PubMed. 49(3). 183–6. 7 indexed citations
16.
BIAGI, G., et al.. (1992). An 1,2,3-triazole derivative bioisoster of a potent in vitro prostaglandin synthesis inhibitor: preparation and biological activity.. PubMed. 47(1). 91–8. 2 indexed citations
17.
BIAGI, G., Oreste Livi, & Antonio Lucacchini. (1985). 1-(4-SUBSTITUTED-BENZYL)-1,2,3-TRIAZOLES, INVITRO INHIBITORS OF PROSTAGLANDIN SYNTHESIS. 20(3). 267–271. 3 indexed citations
18.
Livi, Oreste, et al.. (1983). Synthesis and in vitro antiinflammatory activity of 4-phenyl-1,2,3-triazole derivatives. 18(5). 471–475. 5 indexed citations
19.
Livi, Oreste, et al.. (1979). [Synthesis and pharmacological activity of 1,2,3-triazole derivatives of naphthalene, quinoline and pyridine].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 34(3). 217–28. 3 indexed citations
20.
Livi, Oreste, et al.. (1972). 二,三の1,8-ナフチリジン誘導体のニトロ化. Gazzetta chimica italiana. 102(4). 253–264. 4 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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