Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Gianluca Pardi"'
Autor:
Laura Gatti, Elisabetta Corna, Gianluca Pardi, Cecilia Allievi, Nicoli Paola, Franco Zunino, N. Carenini, Stefano Di Giovine, Jack W. Singer, Mario Grugni, Sergio De Munari, P Apostoli, Marco Natangelo, Gabriella Pezzoni, Paola Perego, Roberto Leone, Ulla Bastrup
Publikováno v:
Molecular Pharmaceutics. 7:207-216
Multinuclear platinum complexes are characterized by a peculiar DNA binding mode and higher cytotoxic potency than the mononuclear complexes, and efficacy against a wide range of preclinical tumor models. To reduce the high irreversible plasma protei
Autor:
Gianluca Pardi, Wayland E. Noland
Publikováno v:
Journal of Heterocyclic Chemistry. 42:1149-1154
Diels-Alder reaction of 2-(E-2-nitroethenyl)-1H-pyrrole (2a) with 1,4-benzoquinone gave the desired benzo[e]indole-6, 9(3H)-dione (4a) in 10% yield versus a 26% yield (lit. 86% [5]) of the known N-methyl compound (4b) from the N-(or 1)-methyl compoun
Autor:
Federico Da Settimo, Giampaolo Primofiore, Francesca Simorini, Antonio Da Settimo, Anna Maria Marini, Gianluca Pardi
Publikováno v:
Scopus-Elsevier
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The synthetic potential of the title compounds benzimidazo[1,2-a]quinazoline-5(7H)-one 2a and 5,7-dihydro-5-oxopyrido[3′,2′:5,6]pyrimido[1,2-a]benzimidazole 2b for the construction of novel polyhetero-cyclic frameworks is reported. Compounds 2a,b
Autor:
Francesca Simorini, Gianluca Pardi, D. Bertini, Giampaolo Primofiore, Anna Maria Marini, Concettina La Motta, Federico Da Settimo, Silvia Salerno, Antonio Da Settimo
Publikováno v:
Journal of Heterocyclic Chemistry. 39:1001-1006
The synthesis of new pyrido[3′,2′:5,6]thiopyrano[3,2-b]indol-5(6H)-ones was accomplished by the Fischer-indole cyclization of some 2,3-dihydro-3-phenylhydrazonothiopyrano[2,3-b]pyridin-4(4H)-ones, obtained from the 2,3-dihydro-3-hydroxymethylenet
Autor:
Anna Maria Marini, Federico Da Settimo, Pier Luigi Ferrarini, Claudio Mori, Antonio Da Settimo, Silvia Salerno, Concettina La Motta, Giampaolo Primofiore, Gianluca Pardi
Publikováno v:
Journal of Heterocyclic Chemistry. 37:379-382
The synthesis of the title compounds 5H, 11H-pyrido[2′,3′:2,3]thiopyrano[4,3-b]indoles was accomplished by the Fischer indole cyclization of some 2,3-dihydrothiopyrano[2,3-b]pyridin-4(4H)-one phenylhydrazones and 7-methyl-2,3-dihydrothiopyrano[2,
Autor:
Silvia Salerno, Antonio Da Settimo, Giampaolo Primofiore, Claudio Mori, Gianluca Pardi, Anna Maria Marini, Pier Luigi Ferrarini, Federico Da Settimo, Concettina La Motta
Publikováno v:
ChemInform. 31
The synthesis of the title compounds 5H, 11H-pyrido[2′,3′:2,3]thiopyrano[4,3-b]indoles was accomplished by the Fischer indole cyclization of some 2,3-dihydrothiopyrano[2,3-b]pyridin-4(4H)-one phenylhydrazones and 7-methyl-2,3-dihydrothiopyrano[2,
Autor:
Silvia Salerno, Gianluca Pardi, Federico Da Settimo, Giampaolo Primofiore, Francesca Simorini, Anna Maria Marini
Publikováno v:
ChemInform. 32
A new synthetic route to build the [1,2,4]triazino[3,4- f]purine nucleus is described. The novel [1,2,4]-triazino[3,4- f]purine-4,6,8(l H,7 H,9 H)-trione derivatives were obtained by condensation of 8-hydrazinotheophylline with appropriate glyoxylic
Publikováno v:
Tetrahedron Letters. 41:7419-7421
A 1,3,5,7-tetraphenyladamantane derivative having three arms terminating with carboxylic acids and a fourth substituted with a 9,10-phenanthrolinyl ligand was prepared as a new kind of molecular linkage to study dynamics of electron injection at the
Autor:
Wayland E. Noland, Gianluca Pardi
Publikováno v:
ChemInform. 37
Autor:
Silvia Salerno, Giampaolo Primofiore, Federico Da Settimo, Anna Maria Marini, Francesca Simorini, Gianluca Pardi
Publikováno v:
Scopus-Elsevier
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A new synthetic route to build the [1,2,4]triazino[3,4- f]purine nucleus is described. The novel [1,2,4]-triazino[3,4- f]purine-4,6,8(l H,7 H,9 H)-trione derivatives were obtained by condensation of 8-hydrazinotheophylline with appropriate glyoxylic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7afd7dee4718146f49582242230196e6
http://hdl.handle.net/11568/177240
http://hdl.handle.net/11568/177240