Regio- and stereo-controlled opening of 2,3-epoxy amines and 2,3-aziridine amines by the commercially available MgBr(2) is described. As reported, this new method could represent a general and useful approach for the preparation of promising intermediates. Moreover, in particular cases, the reaction evolves toward an interesting oxazolidin-2-one structure.

MgBr2-Mediated Opening of 2,3-Three Membered Heterocyclic Amines

Righi G;
2010

Abstract

Regio- and stereo-controlled opening of 2,3-epoxy amines and 2,3-aziridine amines by the commercially available MgBr(2) is described. As reported, this new method could represent a general and useful approach for the preparation of promising intermediates. Moreover, in particular cases, the reaction evolves toward an interesting oxazolidin-2-one structure.
2010
Istituto di Chimica Biomolecolare - ICB - Sede Pozzuoli
METAL-HALIDES
ALPHA_BETA-EPOXY ESTERS
BIOLOGICAL-ACTIVITY
ALCOHOLS
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/162090
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