Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Elisa Piga"'
Autor:
Daniele Donati, Stefano Biondi, Alfredo Paio, Stjepan Mutak, Sergio Lociuro, Elisa Piga, Francesca Cardullo, Dražen Pavlović, Daniele Andreotti
Publikováno v:
ACS Medicinal Chemistry Letters. 5:1133-1137
An efficient synthesis of α-amino-γ-lactone ketolide (3) was developed, which provided a versatile intermediate for the incorporation of a variety of aryl and heteroaryl groups onto the C-21 position of clarithromycin via HBTU-mediated amidation. T
Autor:
Daniele Andreotti, Luca Tarsi, Elisa Piga, Roberto Profeta, Simone Spada, Mario Mattioli, Fabrizio Micheli
Publikováno v:
Synlett. 2008:2283-2286
A novel high-yielding and regioselective method to prepare N-methylpyrazole derivative is reported, by reaction of an N-Boc- and N-Me-substituted hydrazone with an aromatic alkyl ester.
Autor:
Sophie Huss, Araceli Mallo, Alfredo Paio, Jose M. Bueno, Paola Zarantonello, Silvestre Garcı́a-Ochoa, Fabrizio Micheli, Elisa Piga, Esther Fernández
Publikováno v:
Tetrahedron Letters. 43:4741-4745
Herein we describe a straightforward solid-phase synthesis directed towards the preparation of families of asymmetrically disubstituted furazano[3,4-b]pyrazines by stepwise displacement of the two chlorine atoms in 5,6-dichlorofurazano[3,4-b]pyrazine
Publikováno v:
Tetrahedron Letters. 33:2053-2054
Two benzyl groups can be assembled with a chiral shape in the 6 H , 12 H -Dibenzo[ b,f ][1,5]dithiocine structure which can be resolved into its antipods via enantioselective oxidation to the bissulfoxide. The latter affords one single diastereoisome
Autor:
Mohd Hanafiah, Khayriyyah1,2,3 kye@usm.my, Garcia, Mary L.1 Mary.garcia@burnet.edu.au, Barnes, Nadine C.1 Nadine.barnes@burnet.edu.au, Anderson, David A.1,4 David.anderson@burnet.edu.au
Publikováno v:
BMC Research Notes. 10/1/2018, Vol. 11 Issue 1, pN.PAG-N.PAG. 1p. 3 Graphs.
Autor:
Profeta, Roberto, Mattioli, Mario, Micheli, Fabrizio, Piga, Elisa, Spada, Simone, Tarsi, Luca, Andreotti, Daniele
Publikováno v:
Synlett; 2008, Issue 15, p2283-2286, 4p