Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Maurizio Franciotti"'
Autor:
Rosanna Supino, Mario Bigioni, Amalia Cipollone, Michelandrea De Cesare, Claudia Caserini, Fabio Animati, Graziella Pratesi, Anna Maria Casazza, Edith Monteagudo, Marco Berettoni, Stefano Manzini, Franco Zunino, Andrea Madami, Paolo Lombardi, Federico Arcamone, Donatella Polizzi, Carmela Salvatore, Giovanni Capranico, Sabina C. Righetti, Maurizio Franciotti
Publikováno v:
Scopus-Elsevier
Background: Although doxorubicin re mains one of the most effective agent for the treatment of solid tumors, then is an intensive effort to synthesize doxo rubicin analogues (compounds with similar chemical structures) that may have improved antitumo
Publikováno v:
Tetrahedron Letters. 34:1355-1358
Allylsilanes preapared from α-aminoacids react with acyl chlorides in the presence of TiCl4 to give unsaturated amino ketones, easily transformed into pyrrolidine derivatives, whereas addition to aldehydes gave 2,6-disubstituted tetrahydropyridines.
Publikováno v:
ChemInform. 23
Publikováno v:
ChemInform. 23
Publikováno v:
ChemInform. 24
Autor:
Amalia Cipollone, Paolo Lombardi, Fabio Animati, Federico Arcamone, Maurizio Franciotti, Marco Berettoni
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :1327-1329
The synthesis of the new disaccharide anthracyclines 20, 21, 24 and 25, where the daunosamine moiety is separated from the aglycone by either a rhamnose or a fucose residue, performed following a convergent procedure, gives insight into the configura
2-Trimethylsilylethylidentriphenylphosphorane reacts stereoselectively with α-amino aldehydes giving the Cram chelation controlled product of vinylation of the carbonyl group. The olefinic 1,2-amino alcohols obtained with this reaction are important
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2e677acf693278bb9e10864c32da451
http://hdl.handle.net/11365/30959
http://hdl.handle.net/11365/30959