Fausta Ulgheri

527 total citations
24 papers, 408 citations indexed

About

Fausta Ulgheri is a scholar working on Organic Chemistry, Molecular Biology and Pharmaceutical Science. According to data from OpenAlex, Fausta Ulgheri has authored 24 papers receiving a total of 408 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Organic Chemistry, 14 papers in Molecular Biology and 2 papers in Pharmaceutical Science. Recurrent topics in Fausta Ulgheri's work include Carbohydrate Chemistry and Synthesis (12 papers), Chemical Synthesis and Analysis (6 papers) and Asymmetric Synthesis and Catalysis (5 papers). Fausta Ulgheri is often cited by papers focused on Carbohydrate Chemistry and Synthesis (12 papers), Chemical Synthesis and Analysis (6 papers) and Asymmetric Synthesis and Catalysis (5 papers). Fausta Ulgheri collaborates with scholars based in Italy, Netherlands and Brazil. Fausta Ulgheri's co-authors include Pietro Spanu, Gloria Rassu, Giovanni Casiraghi, Luigi Pinna, Oreste Piccolo, Mauro Marchetti, Antonio Saba, Davide Fabbri, Pietro D. Spanu and Giorgio Chelucci and has published in prestigious journals such as Journal of Medicinal Chemistry, The Journal of Organic Chemistry and Tetrahedron.

In The Last Decade

Fausta Ulgheri

24 papers receiving 386 citations

Peers

Fausta Ulgheri

SPECT

PHARM

Roman Davis United States

John S. Ng United States

Mark J. Ford Germany

Kan K. Eng United States

Yoshitaka Araki Japan

Jack Melton Germany

Gregory L. Karrick United States

Sudharshan Madapa India

Paul M. Herrinton United States

Pietro Spanu Italy

Roman Davis United States

Fausta Ulgheri

281 ×0.8

114 ×0.9

64 ×1.1

21 ×0.7

SPECT

26 ×0.9

PHARM

Citations per year, relative to Fausta Ulgheri Fausta Ulgheri (= 1×) peers Roman Davis

Countries citing papers authored by Fausta Ulgheri

Since Specialization

Citations

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

Fields of papers citing papers by Fausta Ulgheri

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fausta Ulgheri

This figure shows the co-authorship network connecting the top 25 collaborators of Fausta Ulgheri. A scholar is included among the top collaborators of Fausta Ulgheri 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 Fausta Ulgheri. Fausta Ulgheri is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Ulgheri, Fausta, Pietro D. Spanu, Giovanni Loriga, et al.. (2021). Design, synthesis and biological evaluation of 1,5-disubstituted α-amino tetrazole derivatives as non-covalent inflammasome-caspase-1 complex inhibitors with potential application against immune and inflammatory disorders. European Journal of Medicinal Chemistry. 229. 114002–114002. 6 indexed citations

Fuggetta, Maria Pia, Pietro D. Spanu, Fausta Ulgheri, et al.. (2019). A New Synthetic Spiroketal: Studies on Antitumor Activity on Murine Melanoma Model In Vivo and Mechanism of Action In Vitro. Anti-Cancer Agents in Medicinal Chemistry. 19(4). 567–578. 1 indexed citations

Fuggetta, Maria Pia, A. DE MICO, Andrea Cottarelli, et al.. (2016). Synthesis and Enantiomeric Separation of a Novel Spiroketal Derivative: A Potent Human Telomerase Inhibitor with High in Vitro Anticancer Activity. Journal of Medicinal Chemistry. 59(19). 9140–9149. 9 indexed citations

Spanu, Pietro, Alberto Mannu, & Fausta Ulgheri. (2014). An unexpected reaction of pyridine with acetyl chloride to give dihydropyridine and piperidine derivatives. Tetrahedron Letters. 55(11). 1939–1942. 6 indexed citations

Spanu, Pietro, et al.. (2010). 5-Trihydroxypropyl-dihydrouracil derivatives as precursors of 1-azasugars: application to the stereoselective synthesis of d-galacto-isofagomine. Tetrahedron Letters. 51(18). 2400–2402. 6 indexed citations

Marchetti, Mario, et al.. (2008). Synthesis of indole derivatives by domino hydroformylation/indolization of 2-nitrocinnamaldehydes. Journal of Molecular Catalysis A Chemical. 288(1-2). 103–108. 4 indexed citations

Spanu, Pietro & Fausta Ulgheri. (2008). Synthetic Approaches to Carbohydrate-Based Ureas. Current Organic Chemistry. 12(13). 1071–1092. 10 indexed citations

Ulgheri, Fausta, Daniela Giunta, & Pietro Spanu. (2008). Short and highly stereoselective total synthesis of d-ribo-configured ureido sugars. Tetrahedron. 64(51). 11768–11775. 8 indexed citations

Ulgheri, Fausta, Mauro Marchetti, & Oreste Piccolo. (2007). Enantioselective Synthesis of (S)- and (R)-Tolterodine by Asymmetric Hydrogenation of a Coumarin Derivative Obtained by a Heck Reaction. The Journal of Organic Chemistry. 72(16). 6056–6059. 85 indexed citations

10.

Ulgheri, Fausta, et al.. (2005). Advances in Asymmetric Synthesis of Biologically Active Molecules Using Heterocycles as Building Blocks. ChemInform. 36(47). 1 indexed citations

11.

Ulgheri, Fausta, et al.. (2003). Diastereoselective synthesis of 5-(alditol-1-C-yl)-hydantoins and their use as precursors of polyhydroxylated-α-amino acids. Tetrahedron Letters. 45(5). 1047–1050. 11 indexed citations

12.

Chelucci, Giorgio, Alessia Bacchi, Davide Fabbri, Antonio Saba, & Fausta Ulgheri. (1999). Enantiomerically pure 1-(2-methoxy-1-naphthyl) and 1-(2-methylthio-1-naphthyl)isoquinoline: two new axially chiral NO and NS ligands for asymmetric catalysis. Tetrahedron Letters. 40(3). 553–556. 29 indexed citations

13.

Chelucci, Giorgio, Daniela Berta, Davide Fabbri, et al.. (1998). Enantioselective addition of diethylzinc to benzaldehyde in the presence of sulfur-containing pyridine ligands. Tetrahedron Asymmetry. 9(11). 1933–1940. 23 indexed citations

14.

Spanu, Pietro, Gloria Rassu, Fausta Ulgheri, et al.. (1996). Divergent synthesis of 3-amino-3-deoxy- and 4-amino-4-deoxyhexoses. Tetrahedron. 52(13). 4829–4838. 12 indexed citations

15.

Casiraghi, Giovanni, Pietro Spanu, Gloria Rassu, Luigi Pinna, & Fausta Ulgheri. (1994). Total Syntheses of All Four Isomers of cis-1,2-Dihydroxypyrrolizidine. The Journal of Organic Chemistry. 59(10). 2906–2909. 42 indexed citations

16.

Rassu, Gloria, Luigi Pinna, Pietro Spanu, Fausta Ulgheri, & Giovanni Casiraghi. (1994). Total syntheses of N-boc-protected 3′-deoxy-4′-azathymidine and 4′-azauridine. Tetrahedron Letters. 35(23). 4019–4022. 42 indexed citations

17.

Rassu, Gloria, Giovanni Casiraghi, Luigi Pinna, et al.. (1993). Efficient total syntheses of (1R, 2R, 3R, 9R, 9aR)-1,2,3,9-tetrahydroxyquinolizidine and its enantiomer. Tetrahedron. 49(30). 6627–6636. 14 indexed citations

18.

Casiraghi, Giovanni, Luigi Pinna, Gloria Rassu, Pietro D. Spanu, & Fausta Ulgheri. (1993). Total synthesis of 2,3-dideoxy-C-methylheptose derivatives. Tetrahedron Asymmetry. 4(4). 681–686. 7 indexed citations

19.

Casiraghi, Giovanni, Fausta Ulgheri, Pietro Spanu, et al.. (1993). Selective reactions using N-(tert-butoxycarbonyl)-2-(tert-butyldimethylsiloxy)pyrrole: concise asymmetric syntheses of (+)-1-deoxy-8-epi-castanospermine and its enantiomer. Journal of the Chemical Society Perkin Transactions 1. 2991–2991. 21 indexed citations

20.

Rassu, Gloria, Luigi Pinna, Pietro Spanu, et al.. (1993). Asymmetric synthesis of 4-amino-2,3,4-trideoxyaldonic acids: novel gaba c-glycoconjugates. Tetrahedron. 49(29). 6489–6496. 10 indexed citations

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