Zobrazeno 1 - 10
of 305
pro vyhledávání: '"M. Capozzi"'
Autor:
Ivana Marino, Eugenia Pignataro, Donatella Danzi, Francesco Cellini, Cosimo Cardellicchio, Antonino Biundo, Isabella Pisano, Maria Annunziata M. Capozzi
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-8 (2022)
Abstract Production of value-added compounds from waste materials is of utmost importance for the development of a sustainable society especially regarding their use as catalysts in industrially relevant synthetic reactions. Herein, we show the produ
Externí odkaz:
https://doaj.org/article/01cc520984614f03b74f0f024ff94783
Publikováno v:
Molbank, Vol 2023, Iss 3, p M1695 (2023)
The complex structure of aminobenzylnaphthols can be easily obtained with the useful Betti reaction. These valuable compounds can give rise to chiral intermediates, that found wide application in asymmetric synthesis. 1-[(1S)-(4-Fluorophenyl)-((1′S
Externí odkaz:
https://doaj.org/article/1d47ef41c7be4d5ca8c3b88f9b040f5d
Publikováno v:
Molbank, Vol 2023, Iss 2, p M1631 (2023)
In the original publication [...]
Externí odkaz:
https://doaj.org/article/1d2808ec188147dfac68c43d6f29e0be
Autor:
Cosimo Cardellicchio, Valentino Laquintana, Rosa Maria Iacobazzi, Nunzio Denora, Antonio Scilimati, Maria Grazia Perrone, Maria Annunziata M. Capozzi
Publikováno v:
Applied Sciences, Vol 13, Iss 21, p 12002 (2023)
Sulindac is a well-known anti-inflammatory agent, sometimes employed as an adjuvant in antitumor therapy. Due to the recent interest in sulfoximine for its potential chemotherapeutics, we decided to transform sulindac and its methyl ester into the co
Externí odkaz:
https://doaj.org/article/0dc77d9710f24c47b89db3560d231821
Publikováno v:
Molbank, Vol 2022, Iss 4, p M1522 (2022)
The Betti reaction of 2-naphthol, benzaldehyde and (S)-1-(4-nitrophenyl)ethylamine without any solvent gave the corresponding aminobenzylnaphthol, that is the (S,S)-1-(phenyl((1′-4-nitrophenyl-ethyl)amino)methyl)-2-naphthol, in good yield (56%). Th
Externí odkaz:
https://doaj.org/article/4b8671705de54f2d9cb41d0212bcdee7
Publikováno v:
Molbank, Vol 2022, Iss 4, p M1528 (2022)
The solvent-free Betti reaction of 2-naphthol, 4-nitrobenzaldehyde and (S)-valine methyl ester gave the corresponding aminobenzylnaphthol of the (S,S)-2-(((hydroxynaphth-1-yl)(4′-nitrophenyl)methyl)amino)-3-methylbutanoic acid methyl ester in good
Externí odkaz:
https://doaj.org/article/653855619ae740b49944179491750ffc
Publikováno v:
Applied Sciences, Vol 12, Iss 15, p 7779 (2022)
Two aminobenzylnaphthols, which are representative items of the family of compounds synthesized with the Betti reaction, were investigated as antiproliferative agents against adenocarcinoma human colorectal (Caco-2) and human neuroblastoma (SH-SY5Y)
Externí odkaz:
https://doaj.org/article/d38d5b22d53f4c719613ddccf595e300
Autor:
Gianluigi Albano, Francesco Zinna, Andrea Taddeucci, Maria Annunziata M. Capozzi, Gennaro Pescitelli, Angela Punzi, Lorenzo Di Bari, Gianluca M. Farinola
We have studied the impact of achiral substituents on the chiral supramolecular architectures of diketopyrrolo[3,4-c]pyrrole-1,2,3-1H-triazole (DPP) dyes. We decorated the same chiral DPP motif with substituent groups on the nitrogen atoms of the lac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a03ee5a4730b33e41bbba5314fb75e2b
https://zenodo.org/record/7885354
https://zenodo.org/record/7885354
Publikováno v:
Green Chemistry. 24:1809-1894
A comprehensive and critical overview of the sustainable strategies for direct C–H bond arylation of (hetero)arenes, based on the use of recoverable catalysts, sustainable solvents and non-conventional energy sources, has been performed.
Autor:
Gianfranco Decandia, Gianluca M. Farinola, Angela Punzi, Gianluigi Albano, Maria Annunziata M. Capozzi, Nicola Zappimbulso
Publikováno v:
Chemsuschem
The increasing attention towards environmentally friendly synthetic protocols has boosted studies directed to the development of green and sustainable methods for direct C−H bond arylation of (hetero)arenes. In this context, here the infrared (IR)