The chemistry underlying how diazabicycloheptanes are assembled is described, subdivided according to chemical structure of two types, the 3,6 diazabicyclo[3.1.1]heptane and the 2,5-diazabicyclo[2.2.1]heptane ring system. Detailed information on myriad of activities of compounds derived from the two scaffolds are reported. © 2012 Bentham Science Publishers.

Synthesis of biologically active bridged diazabicycloheptanes / Murineddu, Gabriele; Asproni, Battistina; Curzu, Maria Michela; Pinna, G; Dore, A; Pau, Amedeo; Deligia, F; Pinna, Gerard Aime. - In: CURRENT MEDICINAL CHEMISTRY. - ISSN 0929-8673. - 19:31(2012), pp. 5342-5363. [10.2174/092986712803833317]

Synthesis of biologically active bridged diazabicycloheptanes

MURINEDDU, Gabriele;ASPRONI, Battistina;CURZU, Maria Michela;PAU, Amedeo;PINNA, Gerard Aime
2012

Abstract

The chemistry underlying how diazabicycloheptanes are assembled is described, subdivided according to chemical structure of two types, the 3,6 diazabicyclo[3.1.1]heptane and the 2,5-diazabicyclo[2.2.1]heptane ring system. Detailed information on myriad of activities of compounds derived from the two scaffolds are reported. © 2012 Bentham Science Publishers.
Synthesis of biologically active bridged diazabicycloheptanes / Murineddu, Gabriele; Asproni, Battistina; Curzu, Maria Michela; Pinna, G; Dore, A; Pau, Amedeo; Deligia, F; Pinna, Gerard Aime. - In: CURRENT MEDICINAL CHEMISTRY. - ISSN 0929-8673. - 19:31(2012), pp. 5342-5363. [10.2174/092986712803833317]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11388/156501
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