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Dive into the research topics where Daniele Donati is active.

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Featured researches published by Daniele Donati.


Journal of The Chemical Society, Chemical Communications | 1994

Carbon–carbon bond formation at the C-4 position of an azetidin-2-one ring by intermolecular radical coupling reactions: a route to tribactams

Alessandro Padova; Stanley M. Roberts; Daniele Donati; Alcide Perboni; Tino Rossi

The β-lactam 4 was linked to the enones 8–10 using a radical reaction mediated by tri-n-butyltin hydride to give the 2,6-disubstituted cyclohexanones 11–16, respectively: 13 was converted into the protected tribactam 18 in two steps.


Archive | 1990

10-(1-Hydroxyethyl)-11-oxo-1-azatricyclo[7.2.0.0.3,8]undec-2-ene-2-carboxylic acid derivatives

Bruno Tamburini; Alcide Perboni; Tino Rossi; Daniele Donati; Daniele Andreotti; Giovanni Gaviraghi; Roberto Carlesso; Claudio Bismara


Archive | 1994

1,5-benzodiazepine derivatives useful as cck or gastrin antagonists

Daniele Donati; Antonella Ursini; Mauro Corsi


Archive | 1992

Antibacterial condensed carbapenemes

Alcide Glaxo Spa Perboni; Daniele Donati; Giorgio Tarzia


Archive | 1990

4-(1'-oxocyclohex-2'-yl)azetidin-2-one derivatives

Bruno Tamburini; Alcide Perboni; Tino Rossi; Daniele Donati; Daniele Andreotti; Giovanni Gaviraghi; Stefano Biondi; Claudio Bismara


Archive | 1990

4-(2-OXO-CYCLOHEXYL) AZETIDINONES

Bruno Tamburini; Alcide Perboni; Tino Rossi; Daniele Donati; Daniele Andreotti; Giovanni Gaviraghi; Stefano Biondi; Claudio Bismara


Archive | 1994

1,5-benzodiazepine derivatives

Daniele Donati; Antonella Ursini; Mauro Corsi


Archive | 1992

Esters of antibacterial condensed carbapenemederivatives.

Giovanni Gaviraghi; Daniele Donati; Giorgio Tarzia; Alcide Glaxo Spa Perboni; Antonella Ursini


Archive | 1990

Derivatives of 1-azatricyclo[7.2.03,8]undec-2-ene-2-carboxyclic acid

Bruno Tamburini; Alcide Perboni; Tino Rossi; Daniele Donati; Daniele Andreotti; Giovanni Gaviraghi; Roberto Carlesso; Claudio Bismara


ChemInform | 2010

Synthesis of a Novel Fluorotribactam Utilizing an N-Fluorosulfonimide in the Key Step.

Alessandro Padova; Stanley M. Roberts; Daniele Donati; C. Marchioro; Alcide Perboni

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