129687-65-6Relevant articles and documents
An anomeric effect drives the regiospecific ring-opening of 1,3-oxazolidines under acetylating conditions
Martinez, R. Fernando,Avalos, Martin,Babiano, Reyes,Cintas, Pedro,Jimenez, Jose L.,Light, Mark E.,Palacios, Juan C.,Perez, Esther M. S.
experimental part, p. 5263 - 5273 (2010/11/02)
A series of oxazolidines derived from tris(hydroxymethyl)-aminomethane (TRIS; 1), have been prepared efficiently. Geometries optimized at the B3LYP/6-31G* level of theory, along with the crystal data of compounds 9 and 12 and NOESY correlations
Genotoxicity in oxazolidine derivatives: influence of the nitro group
Vanelle, P,Meo, MP De,Maldonado, J,Nouguier, R,Crozet, MP,et al.
, p. 241 - 250 (2007/10/02)
Tris-(hydroxymethyl)-aminomethane reacts with various aromatic or heterocyclic aldehydes, leading to new mono- or bicyclic oxazolidine derivatives.The importance of molecular surroundings of the nitro group has been evaluated by the genotoxic study of syn