Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Arianna Amenta"'
Autor:
Antonia I. Antoniou, Giulia Nordio, Maria Luisa Di Paolo, Eleonora Colombo, Beatrice Gaffuri, Laura Polito, Arianna Amenta, Pierfausto Seneci, Lisa Dalla Via, Dario Perdicchia, Daniele Passarella
Publikováno v:
Pharmaceuticals, Vol 16, Iss 5, p 722 (2023)
A potent nontoxic antitumor drug, 2-hydroxyoleic acid (6, 2OHOA) used for membrane lipid therapy, was selected as a self-assembly inducer due to its ability to form nanoparticles (NPs) in water. For this purpose, it was conjugated with a series of an
Externí odkaz:
https://doaj.org/article/989a683bcee348109029a8979ddd23b4
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 24, p 15960 (2022)
In the panorama of sustainable chemistry, the use of green solvents is increasingly emerging for the optimization of more eco-friendly processes which look to a future of biocompatibility and recycling. The green solvent Cyrene, obtained from biomass
Externí odkaz:
https://doaj.org/article/2d3bb69c384b4565900857eb54e8a443
Autor:
Sabrina Giofrè, Antonio Renda, Silvia Sesana, Beatrice Formicola, Barbara Vergani, Biagio Eugenio Leone, Vanna Denti, Giuseppe Paglia, Serena Groppuso, Valentina Romeo, Luca Muzio, Andrea Balboni, Andrea Menegon, Antonia Antoniou, Arianna Amenta, Daniele Passarella, Pierfausto Seneci, Sara Pellegrino, Francesca Re
Publikováno v:
Pharmaceutics, Vol 14, Iss 11, p 2402 (2022)
Dual functionalized liposomes were developed to cross the blood–brain barrier (BBB) and to release their cargo in a pathological matrix metalloproteinase (MMP)-rich microenvironment. Liposomes were surface-functionalized with a modified peptide der
Externí odkaz:
https://doaj.org/article/c466099e0aa34384bb4a567dc44eff87
Publikováno v:
Molecules, Vol 24, Iss 19, p 3551 (2019)
The Pd-catalyzed intramolecular carbene C−H insertion of α-diazo-α-(methoxycarbonyl)acetamides to prepare oxindoles as well as β-lactams was studied. In order to identify what factors influence the selectivity of the processes, we explored how t
Externí odkaz:
https://doaj.org/article/034e1ef697134edb88a3b0fc412cc2db
Publikováno v:
Dipòsit Digital de la UB
Universidad de Barcelona
Universidad de Barcelona
A synthetic method to prepare tetrahydroquinoline-4-carboxylic acid esters has been developed through the transition-metal-catalyzed intramolecular aromatic C-H functionalization of α-diazoesters. Both [{Pd(IMes)(NQ)}2 ] (IMes=1,3-dimesitylimidazol-
Publikováno v:
Chemical Communications. 55:1160-1163
Grubbs catalysts are described as a useful alternative to promote intramolecular carbene C-H insertion from α-diazoesters. Moreover, no competition arises from the possible metathesis reactions on substrates bearing alkene and alkyne moieties. DFT c
Publikováno v:
Molecules
E-Prints Complutense: Archivo Institucional de la UCM
Universidad Complutense de Madrid
Volume 24
Issue 19
Dipòsit Digital de la UB
Universidad de Barcelona
E-Prints Complutense. Archivo Institucional de la UCM
instname
Molecules, Vol 24, Iss 19, p 3551 (2019)
E-Prints Complutense: Archivo Institucional de la UCM
Universidad Complutense de Madrid
Volume 24
Issue 19
Dipòsit Digital de la UB
Universidad de Barcelona
E-Prints Complutense. Archivo Institucional de la UCM
instname
Molecules, Vol 24, Iss 19, p 3551 (2019)
The Pd-catalyzed intramolecular carbene C&ndash
H insertion of &alpha
diazo-&alpha
(methoxycarbonyl)acetamides to prepare oxindoles as well as &beta
lactams was studied. In order to identify what factors influence the selectivity
H insertion of &alpha
diazo-&alpha
(methoxycarbonyl)acetamides to prepare oxindoles as well as &beta
lactams was studied. In order to identify what factors influence the selectivity
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 25(43)
A synthetic method to prepare tetrahydroquinoline-4-carboxylic acid esters has been developed through the transition-metal-catalyzed intramolecular aromatic C-H functionalization of α-diazoesters. Both [{Pd(IMes)(NQ)}
Publikováno v:
Dipòsit Digital de la UB
Universidad de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
instname
Universidad de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
instname
The use of Pd‐, Rh(II)‐ and Ru(II)‐based catalysts has been explored in the transition metal‐catalysed intramolecular carbenoid C−H insertion of α‐diazoesters leading to pyrrolidines. Although the outcome of the reaction was highly subst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d32d4b997352d361dd6b3fa5fd20c95
http://hdl.handle.net/2445/127844
http://hdl.handle.net/2445/127844