104283-67-2Relevant 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
HYDROXY SCHIFF BASE-OXAZOLIDINE TAUTOMERISM: APPARENT BREAKDOWN OF BALDWIN'S RULES
Astudillo, Mario E. Alva,Chokotho, Norris C. J.,Jarvis, Terence C.,Johnson, C. David,Lewis, Colin C.,McDonnell, Peter D.
, p. 5919 - 5928 (2007/10/02)
The tautomerism between hydroxy Schiff bases, X=C6H4CR=NCMe2CH2OH (R=H, Me, C6H5; X is a range of substituents) and X=C6H4CR=NC6H4(o-CH2OH), and the corresponding ring closed systems, oxazolidines and dihydrobenzoxazines, has been investigated.In all case
