Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Elisabetta Piga"'
Autor:
Luigi Lay, Elisabetta Piga, Sergio Castoldi, Giovanni Russo, Massimiliano Cravini, Fabrizio Micheli, Pierfausto Seneci
Publikováno v:
European Journal of Organic Chemistry. 2004:2853-2862
Two tetravalent lactosidic scaffolds have been synthesised in solution from commercial lactose. Careful manipulation of the protecting groups allowed us to orthogonally protect four OH groups for their use as diversity sites for the development of br
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 7:2061-2066
The synthesis and antibacterial activity of some trinems having a sulfur atom in various positions of ring C are presented.
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 6:2791-2794
This article describes studies carried out on the synthesis and biological activity of 4-ureido trinems 1 obtained by the condensation of various isocyanates and the intermedite 6. Among others, 4-N-methyl-N-alkyl ureido trinems showed a promising an
Autor:
David Noble, Stanley M. Roberts, Graham Webb, Tino Rossi, Hugh Marley, Michael J. Dawson, Yam To Ip, Paul Stead, Elisabetta Piga, Mahmoud Mahmoudian
Publikováno v:
Tetrahedron: Asymmetry. 7:2247-2250
Enzymatic and chemical resolution methods suitable for preparation of multi-kg quantities of (+)-(1S,2S)-2-methoxycyclohexanol from (+/−) trans-2-methoxycyclohexanol have been developed. The enzymatic resolution was found to offer a particularly si
Autor:
Daniele Andreotti, Stefano Biondi, Daniele Donati, Tino Rossi, Romano Di Fabio, Elisabetta Piga
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 6:2019-2024
Synthesis of new 4-alkoxy substituted trinems 4, 5, 6, 7 and 8 together with their antibacterial profiles compared to imipenem and GV104326 ( 2 ) are described. The good antibacterial profile observed for derivatives 4–7 encouraged further explorat
Publikováno v:
Tetrahedron Letters. 37:3891-3894
By modulating the reactivity of the Lewis acid promoter it was possible to obtain, in a single stereoselective condensation step, the methoxyketone 7, an advanced intermediate in the synthesis of Sanfetrinem GV104326.
Publikováno v:
ChemInform. 28
This article describes studies carried out on the synthesis and biological activity of 4-ureido trinems 1 obtained by the condensation of various isocyanates and the intermedite 6. Among others, 4-N-methyl-N-alkyl ureido trinems showed a promising an
Publikováno v:
ChemInform. 27
Publikováno v:
ChemInform. 27
By modulating the reactivity of the Lewis acid promoter it was possible to obtain, in a single stereoselective condensation step, the methoxyketone 7, an advanced intermediate in the synthesis of Sanfetrinem GV104326.
Publikováno v:
ChemInform. 28
The synthesis and antibacterial activity of some trinems having a sulfur atom in various positions of ring C are presented.