Francesca Quartieri
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Explore the profile of Francesca Quartieri including associated specialties, affiliations and a list of published articles.
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9
Citations
121
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Recent Articles
1.
Brunelli F, Quartieri F, Miletto I, Pulici M, Papeo G, Tron G
Chemistry
. 2024 Aug;
30(50):e202402175.
PMID: 39166444
The facile generation of the α-acyloxy carboxamide radical is hereby reported for the first time, utilizing a photoredox catalyzed reaction of Passerini adducts synthesized using a 4-formyl-1,4-dihydropyridine as the carbonyl...
2.
Quartieri F, Nesi M, Avanzi N, Borghi D, Casale E, Corti E, et al.
Bioorg Med Chem Lett
. 2021 Aug;
51:128310.
PMID: 34416377
In this article we describe the identification of unprecedented ATP-competitive ChoKα inhibitors starting from initial hit NMS-P830 that binds to ChoKα in an ATP concentration-dependent manner. This result is confirmed...
3.
Papeo G, Avanzi N, Bettoni S, Leone A, Paolucci M, Perego R, et al.
J Biomol Screen
. 2014 Jun;
19(8):1212-9.
PMID: 24916412
PARP inhibitors are an exciting new class of antineoplastic drugs that have been proven to be efficacious as single agents in cancer settings with inherent DNA repair defects, as well...
4.
Piutti C, Quartieri F
Molecules
. 2013 Oct;
18(10):12290-312.
PMID: 24108396
Nearly forty years ago, at the University of Rome, Giovanni Piancatelli and co-workers discovered the acid-catalyzed water-mediated rearrangement of 2-furylcarbinols into 4-hydroxycyclopentenones. These motifs are core components of several pharmacologically...
5.
Caldarelli M, Angiolini M, Disingrini T, Donati D, Guanci M, Nuvoloni S, et al.
Bioorg Med Chem Lett
. 2011 Jul;
21(15):4507-11.
PMID: 21723120
The synthesis and SAR of a series of novel pyrazolo-quinazolines as potent and selective MPS1 inhibitors are reported. We describe the optimization of the initial hit, identified by screening the...
6.
Forte B, Malgesini B, Piutti C, Quartieri F, Scolaro A, Papeo G
Mar Drugs
. 2010 Jan;
7(4):705-53.
PMID: 20098608
In his most celebrated tale "The Picture of Dorian Gray", Oscar Wilde stated that "those who go beneath the surface do so at their peril". This sentence could be a...
7.
Brasca M, Amboldi N, Ballinari D, Cameron A, Casale E, Cervi G, et al.
J Med Chem
. 2009 Jul;
52(16):5152-63.
PMID: 19603809
The discovery of a novel class of inhibitors of cyclin dependent kinases (CDKs) is described. Starting from compound 1, showing good potency as inhibitor of CDKs but being poorly selective...
8.
Malgesini B, Forte B, Borghi D, Quartieri F, Gennari C, Papeo G
Chemistry
. 2009 Jun;
15(32):7922-7929.
PMID: 19562787
A total synthesis of the tripeptide alkaloid (-)-chaetominine (1) was achieved in 9.3% overall yield starting from commercially available D-tryptophan methyl ester, based on a short and straightforward (nine steps)...
9.
Trifluoroacetic anhydride-mediated solid-phase version of the Robinson-Gabriel synthesis of oxazoles
Pulici M, Quartieri F, Felder E
J Comb Chem
. 2005 May;
7(3):463-73.
PMID: 15877475
A traceless solid-phase synthesis of oxazoles 4 via Robinson-Gabriel reaction of solid-supported alpha-acylamino ketones 2 has been achieved. The reaction requires that the cyclization precursor be linked to a benzhydrylic-type...