1236068-33-9Relevant academic research and scientific papers
MgBr2-mediated opening of 2,3-three membered heterocyclic amines
Righi, Giuliana,Ciambrone, Simona,Esuperanzi, Evelina,Montini, Francesca,Pelagalli, Romina
, p. 564 - 568 (2010)
(Chemical Equation Presented) Regio- and stereo-controlled opening of 2,3-epoxy amines and 2,3-aziridine amines by the commercially available MgBr2 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.
New highly efficient stereoselective synthesis of d-threo-PDMP
Righi, Giuliana,Bovicelli, Paolo,Montini, Francesca,Meloni, Federica,Mandic, Emanuela,Pelagalli, Romina
, p. 3318 - 3322 (2011/11/30)
Starting from a suitably functionalized aziridine, a highly efficient stereoselective synthesis of (1R,2R)-phenyl-2-decanoyl-amino-3-morpholinopropan- 1-ol (d-threo-PDMP) is described. The approach, based on the ring expansion of the aziridine ring to oxa
