L Gentilucci
Overview
Explore the profile of L Gentilucci including associated specialties, affiliations and a list of published articles.
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7
Citations
38
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Recent Articles
1.
Gentilucci L, Tolomelli A, De Marco R, Artali R
Curr Med Chem
. 2012 Mar;
19(11):1587-601.
PMID: 22376035
In the last years, molecular docking emerged as a powerful tool to investigate the interactions between opioid ligands and their receptors, thus driving the design and development of new selective...
2.
Buscicchio G, Gentilucci L, Baldini E, Giannubilo S, Tranquilli A
Gynecol Endocrinol
. 2009 Jun;
25(10):679-82.
PMID: 19544116
Objective: To investigate fetal heart rate (FHR) of fetuses whose mothers are under levothyroxin treatment for chronic hypothyroidism. Study Design: Sixty women under chronic therapy with levothyroxin and 180 controls...
3.
Cardillo G, Gentilucci L, Tolomelli A
Mini Rev Med Chem
. 2006 Mar;
6(3):293-304.
PMID: 16515468
This review covers our recent advances in the synthesis of unusual amino acids in optically pure form, and their introduction into naturally occurring peptides with specific biological properties, or into...
4.
Cardillo G, Gentilucci L, Gianotti M, PERCIACCANTE R, Tolomelli A
J Org Chem
. 2001 Dec;
66(25):8657-60.
PMID: 11735554
No abstract available.
5.
Cardillo G, Gentilucci L, Gianotti M, Tolomelli A
Org Lett
. 2001 May;
3(8):1165-7.
PMID: 11348185
[reaction: see text]. The 1,4-addition of O-benzylhydroxylamine to alpha,beta-unsaturated imide 1 in the presence of BF3.Et2O proceeds with the preferential attack of the nucleophile on the Cbeta-re face. To explain...
6.
Cardillo G, Gentilucci L, Melchiorre P, Spampinato S
Bioorg Med Chem Lett
. 2001 Jan;
10(24):2755-8.
PMID: 11133084
Endomorphin-1 (Tyr-Pro-Trp-PheNH2) has been proposed as the most potent endogenous ligand of the mu-opioid receptors. In this paper, we describe the synthesis of some endomorphin-1 based tetrapeptides in which a...
7.
Armaroli S, Cardillo G, Gentilucci L, Gianotti M, Tolomelli A
Org Lett
. 2000 May;
2(8):1105-7.
PMID: 10804565
[formula: see text] trans-Aziridine-2-carboxylic acid derivatives are useful intermediates for the synthesis of threonine or allo-threonine through ring expansion and SN2 displacement, respectively. We describe here the preparation of the...