Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Daniele Canestrari"'
Autor:
Andrea Aramini, Gianluca Bianchini, Samuele Lillini, Mara Tomassetti, Niccolò Pacchiarotti, Daniele Canestrari, Pasquale Cocchiaro, Rubina Novelli, Maria Concetta Dragani, Ferdinando Palmerio, Simone Mattioli, Simone Bordignon, Michele d’Angelo, Vanessa Castelli, Francesco d’Egidio, Sabatino Maione, Livio Luongo, Serena Boccella, Annamaria Cimini, Laura Brandolini, Michele Remo Chierotti, Marcello Allegretti
Publikováno v:
Biomedicine & Pharmacotherapy. 163:114845
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::04e2dcddb40baed21193afe28da74bda
https://doi.org/10.1016/j.biopha.2023.114845
https://doi.org/10.1016/j.biopha.2023.114845
Autor:
Samuele Lillini, Serena Gabrielli, Federico Vittorio Rossi, Andrea Aramini, Enrico Marcantoni, Gabriele Lupidi, Gianluca Bianchini, Mara Tomassetti, Daniele Canestrari
The aim of this opinion article is to highlight the trends in the development of efficient catalyst-free synthesis of the Hantzsch polysubstituted 1,3-thiazoles. They are heterocycles of particular importance in the pharmaceutical industry, and the s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::099f33f18fe49403855e9a32b576c9b1
https://doi.org/10.9734/bpi/cacb/v8/9618d
https://doi.org/10.9734/bpi/cacb/v8/9618d
Autor:
John E. O'Brien, Caterina Cioffi, Lorenza Ghisu, Manuel Ruether, Ilaria Biancofiore, Daniele Canestrari, Stefano Lancianesi, Mauro F. A. Adamo, Hasim Ibrahim
Publikováno v:
Chemical Science
Canestrari, Daniele ORCID: 0000-0002-3245-6630, Cioffi, Caterina, Biancofiore, Ilaria, Lancianesi, Stefano, Ghisu, Lorenza, Ruether, Manuel, O'Brien, John, Adamo, Mauro F.A. ORCID: 0000-0001-9072-3648 and Ibrahim, Hasim ORCID: 0000-0003-1386-3641 (2019) Sulphide as a leaving group: highly stereoselective bromination of alkyl phenyl sulphides. Chemical Science, 10 (39). ISSN 2041-6520
Canestrari, Daniele ORCID: 0000-0002-3245-6630
A conceptionally novel nucleophilic substitution approach to synthetically important alkyl bromides is presented. Using molecular bromine (Br2), readily available secondary benzyl and tertiary alkyl phenyl sulphides are converted into the correspondi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c10ef6e83d3dad3ccf2136d457ca2fc5
https://doi.org/10.1039/c9sc03560e
https://doi.org/10.1039/c9sc03560e
Autor:
Eider Badiola, Hasim Ibrahim, Mauro F. A. Adamo, Daniele Canestrari, Stefano Lancianesi, Chiara Strinna
Publikováno v:
Organic letters. 19(4)
The chlorination of readily available secondary and tertiary alkyl phenyl sulfides using (dichloroiodo)benzene (PhICl2) is reported. This mild and rapid nucleophilic chlorination is extended to sulfa-Michael derived sulfides, affording elimination-se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fe2b453084ea5c471225496bf5a7bce
https://pubmed.ncbi.nlm.nih.gov/28151676
https://pubmed.ncbi.nlm.nih.gov/28151676