Luca Banfi
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Explore the profile of Luca Banfi including associated specialties, affiliations and a list of published articles.
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47
Citations
219
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Recent Articles
1.
Vitali Forconesi G, Basso A, Banfi L, Gugliotta D, Lambruschini C, Nola M, et al.
Molecules
. 2024 Apr;
29(8).
PMID: 38675534
Bengamide E is a bioactive natural product that was isolated from Jaspidae sponges by Crews and co-workers in 1989. It displays a wide range of biological activities, including antitumor, antibiotic,...
2.
Raboni F, Galatini A, Banfi L, Riva R, Pellis A
Chembiochem
. 2024 Jan;
25(6):e202300839.
PMID: 38265820
Switching from oil-based to bio-based feedstocks to ensure the green transition to a sustainable and circular future is one of the most pressing challenges faced by many industries worldwide. For...
3.
4.
Pinna A, Basso A, Lambruschini C, Moni L, Riva R, Rocca V, et al.
RSC Adv
. 2022 May;
10(2):965-972.
PMID: 35494435
Starting from easily accessible chiral enantiopure 1,2-amino alcohols and salicylaldehydes, a concise route to cyclic imines has been developed. These chiral cyclic imines undergo a highly diastereoselective Ugi-Joullié reaction to...
5.
Banfi L, Basso A, Lambruschini C, Moni L, Riva R
Chem Sci
. 2022 Jan;
12(47):15445-15472.
PMID: 35003575
This perspective aims at celebrating the 100th anniversary of the discovery of the Passerini three component reaction. After being nearly neglected for many years, now this reaction has become quite...
6.
Vitali Forconesi G, Banfi L, Basso A, Lambruschini C, Moni L, Riva R
Molecules
. 2020 Jul;
25(14).
PMID: 32679733
A chiral bio-based building block, prepared by the lipase-mediated desymmetrization of an erythritol derivative, was further functionalized and then submitted to stereoselective Passerini reactions, allowing the synthesis of a small...
7.
Tomaselli S, La Vitola P, Pagano K, Brandi E, Santamaria G, Galante D, et al.
ACS Chem Neurosci
. 2019 Oct;
10(11):4462-4475.
PMID: 31603646
In this study natural-based complex polyphenols, obtained through a smart synthetic approach, have been evaluated for their ability to inhibit the formation of Aβ oligomers, the most toxic species causing...
8.
Galante D, Banfi L, Baruzzo G, Basso A, DArrigo C, Lunaccio D, et al.
Molecules
. 2019 Jul;
24(14).
PMID: 31331116
While plant polyphenols possess a variety of biological properties, exploration of chemical diversity around them is still problematic. Here, an example of application of the Ugi multicomponent reaction to the...
9.
Lambruschini C, Basso A, Banfi L
Drug Discov Today Technol
. 2018 Nov;
29:3-9.
PMID: 30471671
While often multicomponent reactions (MCR) are used for the diversity-oriented synthesis of racemic (or achiral) molecular entities, this short review describes two alternative approaches for accessing enantiopure products exploiting the...
10.
Lambruschini C, Villa S, Banfi L, Canepa F, Morana F, Relini A, et al.
Beilstein J Nanotechnol
. 2018 May;
9:986-999.
PMID: 29719751
Magnetite-based magnetic nanoparticles have been successfully coupled to an organic system constituted of a fluorescent molecule, a tripeptide specifier and a spacer. The system is able to selectively release the...