Zobrazeno 1 - 10
of 78
pro vyhledávání: '"Francesco, Fini"'
Autor:
Maria Luisa Introvigne, Trevor J. Beardsley, Micah C. Fernando, David A. Leonard, Bradley J. Wallar, Susan D. Rudin, Magdalena A. Taracila, Philip N. Rather, Jennifer M. Colquhoun, Shaina Song, Francesco Fini, Kristine M. Hujer, Andrea M. Hujer, Fabio Prati, Rachel A. Powers, Robert A. Bonomo, Emilia Caselli
Publikováno v:
Antibiotics, Vol 12, Iss 4, p 644 (2023)
Acinetobacter baumannii is a Gram-negative organism listed as an urgent threat pathogen by the World Health Organization (WHO). Carbapenem-resistant A. baumannii (CRAB), especially, present therapeutic challenges due to complex mechanisms of resistan
Externí odkaz:
https://doaj.org/article/0bf39937c44f473185677dc4d7075b7e
Autor:
Samuele Peppoloni, Eva Pericolini, Bruna Colombari, Diego Pinetti, Claudio Cermelli, Francesco Fini, Fabio Prati, Emilia Caselli, Elisabetta Blasi
Publikováno v:
Frontiers in Microbiology, Vol 11 (2020)
Pseudomonas aeruginosa is a Gram-negative nosocomial pathogen, often causative agent of severe device-related infections, given its great capacity to form biofilm. P. aeruginosa finely regulates the expression of numerous virulence factors, including
Externí odkaz:
https://doaj.org/article/dc14461cda4f4fa4b42eaaf71e00de45
Autor:
Giuliana Giorgianni, Luca Bernardi, Francesco Fini, Fabio Pesciaioli, Francesco Secci, Armando Carlone
Enantioselective organocatalysis has quickly established itself as the third pillar of asymmetric catalysis. It is a powerful technology platform, and it has a tremendous impact in both academic and industrial settings. By focusing on pregabalin, as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a05e52d299b659809be51c541a24028
https://hdl.handle.net/11380/1287646
https://hdl.handle.net/11380/1287646
Autor:
Mattia Stucchi, Alessandro Zanni, Maria Luisa Introvigne, Francesco Fini, Emilia Caselli, Fabio Prati
Publikováno v:
Organicbiomolecular chemistry. 19(30)
A straightforward concise synthesis of chiral non-racemic aliphatic α-boryl isocyanides, relay intermediates for boron-based bioactive molecules in multicomponent reactions, is presented. The short synthetic sequence comprises as key steps copper-ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8a0ff2c4887e59be274b8577d0340ef
https://pubmed.ncbi.nlm.nih.gov/34286797
https://pubmed.ncbi.nlm.nih.gov/34286797
Autor:
Fabio Pesciaioli, Francesco Fini, Francesca Della Penna, Arianna Sinibaldi, Marco Ponzetti, Silvia Marchesan, Armando Carlone, Andrea Baschieri
Self-assembling minimalistic peptides embedded with an organocatalytic moiety were designed. By controlling the formation of fibrils via external intervention, it was shown that the activation is accelerated when the organocatalyst is in its supramol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::179dea0be3ddeb6ab3677c6ef4f561b7
https://hdl.handle.net/11368/2997541
https://hdl.handle.net/11368/2997541
Autor:
Giovanni Filippo Palmieri, Luca Casettari, Alessandra Cambriani, Mattia Tiboni, Marco Cespi, Diego Romano Perinelli, Giulia Bonacucina, Francesco Fini
PLGA-PEG-PLGA are copolymers, able to form temperature-dependent hydrogels or sol dispersions at selective conditions. A general overview about the rheological characterization of their aqueous dispersions, focusing how the structural characteristics
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fc5863f20d8ebb46b0501b0136728d8
https://www.sciencedirect.com/science/article/pii/S0032386120310417
https://www.sciencedirect.com/science/article/pii/S0032386120310417
Publikováno v:
Methodologies in Amine Synthesis
This chapter covers the emerging utilization of organocatalytic methodologies in industrial settings directed at the large-scale preparation of enantioenriched amines and N-heterocycles. First, some selected manufacturing processes, based on organoca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8744191fb78872dfa2389bd1ea8415eb
http://hdl.handle.net/11585/852140
http://hdl.handle.net/11585/852140
Autor:
Emilia, Caselli, Francesco, Fini, Maria Luisa, Introvigne, Mattia, Stucchi, Magdalena A, Taracila, Erin R, Fish, Kali A, Smolen, Philip N, Rather, Rachel A, Powers, Bradley J, Wallar, Robert A, Bonomo, Fabio, Prati
Publikováno v:
ACS Infectious Diseases
Boronic acid transition state inhibitors (BATSIs) are known reversible covalent inhibitors of serine β-lactamases. The selectivity and high potency of specific BATSIs bearing an amide side chain mimicking the β-lactam’s amide side chain are an es
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::34812069af6eb8723aac7345f8bab6e1
https://pubmed.ncbi.nlm.nih.gov/32502340
https://pubmed.ncbi.nlm.nih.gov/32502340