Publication Date:
2018
abstract:
[Figure not available: see fulltext.] A convenient synthesis of 2- and/or 3-oxazolines has been developed depending on the structure and stereochemistry of the starting amino alcohol. PhI(OAc)2acted as oxidant on the intermediate imine, as supported by NMR investigation. The findings demonstrate a new route providing access to unusual 3-oxazolines.
Iris type:
1.1 Articolo in rivista
Keywords:
2-oxazolines; 3-oxazolines; hypervalent iodine; NMR studies; stereoselective synthesis; Organic Chemistry
List of contributors:
Carlucci, Claudia; Tota, Arianna; Colella, Marco; Ronamazzi, Giuseppe; Clarkson, Guy J.; Luisi, Renzo; Degennaro, Leonardo
Published in: