Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Chiara Caneva"'
Autor:
Andrea Spallarossa, Matteo Lusardi, Chiara Caneva, Aldo Profumo, Camillo Rosano, Marco Ponassi
Publikováno v:
Molecules, Vol 26, Iss 3, p 557 (2021)
Pyrimido-pyrimidine derivatives have been developed as rigid merbarone analogues. In a previous study, these compounds showed potent antiproliferative activity and efficiently inhibited topoisomerase IIα. To further extend the structure–activity r
Externí odkaz:
https://doaj.org/article/7289d19e623f46bb9e6c0b4579899df0
Autor:
Aldo Profumo, Matteo Lusardi, Chiara Caneva, Marco Ponassi, Andrea Spallarossa, Camillo Rosano
Publikováno v:
Molecules
Volume 26
Issue 3
Molecules, Vol 26, Iss 557, p 557 (2021)
Volume 26
Issue 3
Molecules, Vol 26, Iss 557, p 557 (2021)
Pyrimido-pyrimidine derivatives have been developed as rigid merbarone analogues. In a previous study, these compounds showed potent antiproliferative activity and efficiently inhibited topoisomerase II&alpha
To further extend the structure&ndas
To further extend the structure&ndas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddbcede7f9d5ad93ad499cd88435dd1e
https://doi.org/10.3390/molecules26030557
https://doi.org/10.3390/molecules26030557
Autor:
Chiara Caneva, Roberta Loddo, Ilenia Delogu, Andrea Spallarossa, Cristina Ibba, Monica De Maria, Silvana Alfei
Publikováno v:
Molecular Diversity. 19:669-684
An unprecedented, highly convergent, high-yielding, one-pot synthesis of (acyl)hydrazones and thiosemicarbazones was carried out by the in situ condensation of isolable iminium chlorides of imidazolidin-2-(thio)one, tetrahydropyrimidin-2-thione and i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48b3ac4cc8acb843983d9fb9c722223c
https://doi.org/10.1007/s11030-015-9597-z
https://doi.org/10.1007/s11030-015-9597-z
Autor:
Margherita Brindisi, Silvana Alfei, Stefania Butini, Giuseppina Sanna, Sandra A. Bright, Sandra Gemma, Daniela M. Zisterer, Andrea Spallarossa, Matteo Caviglia, Giuseppe Campiani, Giovanni Maga, Chiara Caneva, Gabriella Collu, Emmanuele Crespan, Clive D. Williams, Roberta Loddo, Ilenia Delogu
A new series of indole-based analogues were recently identified as potential anticancer agents. The Knoevenagel-type indoles herein presented were prepared via a one-pot condensation of iminium salts with active methylene reagents and were isolated a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d59555a27804b7fa8466c9ee1b7b2e96
http://hdl.handle.net/11588/771076
http://hdl.handle.net/11588/771076
Autor:
Andrea Spallarossa, Chiara Caneva, Angelo Ranise, Matteo Caviglia, Francesco Lucchesini, Silvana Alfei
Publikováno v:
ChemInform. 45
Et3N-mediated condensation of preformed or in situ generated indole iminium salts with active methylene reagents provides stereoselectively Knoevenagel-type indoles in moderate to good yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0caf8a81a32e72691d7a98e891ab905
https://doi.org/10.1002/chin.201422124
https://doi.org/10.1002/chin.201422124
Autor:
Angelo Ranise, Francesco Lucchesini, Andrea Spallarossa, Silvana Alfei, Matteo Caviglia, Chiara Caneva
A simple one-pot procedure for the stereoselective synthesis of Knoevenagel-type indoles is described. The method is based on the in situ reaction of indole iminium salts (four of them are fully characterized) with acyclic symmetrical and unsymmetric
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3152c420a5970cd8758b90e8ab4f9f9c
http://hdl.handle.net/11567/644370
http://hdl.handle.net/11567/644370