Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Alessio Sferrazza"'
Autor:
Giacomo Paonessa, Giulia Siciliano, Rita Graziani, Cristiana Lalli, Ottavia Cecchetti, Cristina Alli, Roberto La Valle, Alessia Petrocchi, Alessio Sferrazza, Monica Bisbocci, Mario Falchi, Carlo Toniatti, Alberto Bresciani, Pietro Alano
Publikováno v:
Communications Biology, Vol 5, Iss 1, Pp 1-10 (2022)
High-throughput screening of 120,000 compounds followed by counter-screening and validation assays reveals candidate antimalarial drugs that kill Plasmodium falciparum sexual and asexual blood stages blocking parasite transmission through mosquito.
Externí odkaz:
https://doaj.org/article/59fe7c35684348d7a872e3a5b86d2bef
Autor:
Antonia Iazzetti, Giancarlo Fabrizi, Antonella Goggiamani, Federico Marrone, Alessio Sferrazza, Karim Ullah
Publikováno v:
Molecules, Vol 28, Iss 15, p 5831 (2023)
A gold-catalyzed protocol to obtain functionalized 3H-pyrrolo [1,2,3-de] quinoxalines from suitable substituted N-alkynyl indoles has been proposed. The mild reaction conditions were revealed to be compatible with different functional groups, includi
Externí odkaz:
https://doaj.org/article/de38fcc10537413a9e0f32b796ca363e
Autor:
Antonia Iazzetti, Dario Allevi, Andrea Calcaterra, Giancarlo Fabrizi, Antonella Goggiamani, Giulia Mazzoccanti, Alessio Sferrazza, Rosanna Verdiglione, Valeria Vergine
Publikováno v:
Molecules, Vol 28, Iss 1, p 300 (2022)
The gold-catalyzed cyclization of 2,2-bis(3-arylprop-2-yn1-yl)malonic acid has been proposed as an efficient approach to substituted 3,8-dibenzyl-2,7-dioxaspiro[4.4]nonane-1,6-diones. The reaction proceeds smoothly in mild reaction conditions to give
Externí odkaz:
https://doaj.org/article/4b5a7351ca5b4c988ff8acac65fedab9
Autor:
Antonia Iazzetti, Antonio Arcadi, Stefano Dessalvi, Giancarlo Fabrizi, Antonella Goggiamani, Federico Marrone, Andrea Serraiocco, Alessio Sferrazza, Karim Ullah
Publikováno v:
Catalysts, Vol 12, Iss 12, p 1516 (2022)
A straightforward assembly of polysubstituted 1,2-dihydro-3H-pyrrolo[1,2-a]indol-3-ones through a domino palladium-catalyzed reaction of indol-2-ylmethyl acetates with 1,3-dicarbonyl derivatives is described. The key role of the features of the 1,3-d
Externí odkaz:
https://doaj.org/article/fd3cb79630bb43318850898f29abad34
Autor:
Esther Torrente, Valentina Fodale, Alina Ciammaichella, Federica Ferrigno, Jesus M. Ontoria, Simona Ponzi, Ilaria Rossetti, Alessio Sferrazza, Jérôme Amaudrut, Antonino Missineo, Simone Esposito, Simone Palombo, Martina Nibbio, Mauro Cerretani, Monica Bisbocci, Antonella Cellucci, Annalise di Marco, Cristina Alli, Vincenzo Pucci, Carlo Toniatti, Alessia Petrocchi
Publikováno v:
ACS Medicinal Chemistry Letters. 14:156-162
Autor:
Antonella Goggiamani, Antonio Arcadi, Alessia Ciogli, Martina De Angelis, Stefano Dessalvi, Giancarlo Fabrizi, Federica Iavarone, Antonia Iazzetti, Alessio Sferrazza, Roberta Zoppoli
Publikováno v:
RSC Advances. 13:10090-10096
The synthesis of 2,3-dihydropyrazino[1,2-a]indol-4(1H)-ones through the in situ generation of 2-methide-2H-indole intermediate I starting from 2-indolylmethyl acetates under basic conditions/nucleophilic Michael addition/cyclization cascade reaction.
Autor:
Paola Fezzardi, Danilo Fabbrini, Nicola Relitti, Federica Ferrigno, Ilaria Rossetti, Alessio Sferrazza, Alessia Petrocchi, Christian Montalbetti
Publikováno v:
Tetrahedron Letters. 97:153789
Autor:
Alberto Bresciani, Alessio Sferrazza, Matteo Andreini, Steven J. Harper, Rita Graziani, Danilo Fabbrini, Emanuela Nizi, Giacomo Paonessa, Valentina Nardi, Nadia Gennari
Publikováno v:
Bioorganicmedicinal chemistry letters. 28(9)
Falcipain-2 (FP2) is an essential enzyme in the lifecycle of malaria parasites such as Plasmodium falciparum, and its inhibition is viewed as an attractive mechanism of action for new anti-malarial agents. Selective inhibition of FP2 with respect to
Publikováno v:
Current organic chemistry 19 (2015): 99–104. doi:10.2174/1385272819666141211221640
info:cnr-pdr/source/autori:Sferrazza, Alessio; Triolo, Alessandro; Migneco, Luisa M.; Caminiti, Ruggero/titolo:Synthesis and Small and Wide Angle X-Ray Scattering Characterization of L-Proline Based Chiral Ionic Liquids/doi:10.2174%2F1385272819666141211221640/rivista:Current organic chemistry/anno:2015/pagina_da:99/pagina_a:104/intervallo_pagine:99–104/volume:19
Scopus-Elsevier
info:cnr-pdr/source/autori:Sferrazza, Alessio; Triolo, Alessandro; Migneco, Luisa M.; Caminiti, Ruggero/titolo:Synthesis and Small and Wide Angle X-Ray Scattering Characterization of L-Proline Based Chiral Ionic Liquids/doi:10.2174%2F1385272819666141211221640/rivista:Current organic chemistry/anno:2015/pagina_da:99/pagina_a:104/intervallo_pagine:99–104/volume:19
Scopus-Elsevier
In this work we report the first small and wide-angle X-Ray diffraction study (S-WAXS) of L-proline ester based ionic liquids, a family of chiral ionic liquids (CILs) with several potential useful applications. Along the synthetic pathway that was fo
Publikováno v:
Angewandte Chemie International Edition. 49:4067-4070
The title compounds are alkynylated by a domino iododediazoniation/Sonogashira cross-coupling using various terminal alkynes and a variety of functionalities is tolerated for both types of substrates.