Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Antonella Ilenia Alfano"'
Autor:
Sveva Pelliccia, Antonella Ilenia Alfano, Beatriz Ramos Gomes Da Assunção, Luigia Turco, Francesca Lembo, Vincenzo Summa, Elisabetta Buommino, Margherita Brindisi
Publikováno v:
Frontiers in Chemistry, Vol 11 (2023)
The [1,2,3]-triazolo [1,5-a] quinoxalin-4(5H)-one scaffold and its analogues triazole-fused heterocyclic compounds are relevant structural templates in both natural and synthetic biologically active compounds. However, their medicinal chemistry appli
Externí odkaz:
https://doaj.org/article/6bf770e98cbd4144a7b6499ba99d96e3
Publikováno v:
Journal of Medicinal Chemistry. 65:3080-3097
Compelling new support has been provided for histone deacetylase isoform 6 (HDAC6) as a common thread in the generation of the dysregulated proinflammatory and fibrotic phenotype in cystic fibrosis (CF). HDAC6 also plays a crucial role in bacterial c
Autor:
Maria Grazia Ferraro, Antonella Ilenia Alfano, Angela Zampella, Heiko Lange, Elisabetta Buommino, Carlo Irace, Margherita Brindisi
Publikováno v:
ChemMedChem. 16:3795-3809
The generation of peptidomimetic substructures for medicinal chemistry purposes requires effective and divergent synthetic methods. We present in this work an efficient flow process that allows quick modulation of reagents for Joullié-Ugi multicompo
Publikováno v:
ChemSusChem. 15
Publikováno v:
ChemSusChem. 15
Formation of amide bonds is of immanent importance in organic and synthetic medicinal chemistry. Its presence in “traditional” small-molecule active pharmaceutical ingredients, in linear or cyclic oligo- and polypeptidic actives, including pseudo
Autor:
Fabiola Fanini, Alberto Luridiana, Daniele Mazzarella, Antonella Ilenia Alfano, Perry van der Heide, Juan A. Rincón, Pablo García-Losada, Carlos Mateos, Michael O. Frederick, Manuel Nuño, Timothy Noël
Publikováno v:
Tetrahedron Letters. 117:154380
Autor:
Antonella Ilenia Alfano, Davide Ravelli, Gian Cesare Tron, Sveva Pelliccia, Mariateresa Giustiniano, Ettore Novellino, Alberto Massarotti, Paolo Luciano
Publikováno v:
The Journal of Organic Chemistry. 85:1981-1990
A visible-light-promoted three-component isocyanide-based synthesis of iminofurans is herein reported. The reaction proved to be general in scope and proceeds through a triple domino process. Control experiments with 18O-labeled water and TEMPO provi
Privileged scaffolds as starting points toward biologically active molecules represent a neuralgic point in drug discovery. The ability of synthetic chemists concerned with their generation should be flanked by robust technologies enabling the effici
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96ce41e265f62fb75b5a9541ca34cd3c
http://hdl.handle.net/10281/316864
http://hdl.handle.net/10281/316864
A greener and sustainable flow chemistry protocol for the synthesis of 3,3-disubstituted indolenines through interrupted Fischer indolisation reaction is described. First, two model aldehydes were reacted with phenylhydrazine in order to explore the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e6fa77e7919ac054f8c68c24c915c34
http://hdl.handle.net/10281/316890
http://hdl.handle.net/10281/316890