REVUE ROUMAINE DE CHIMIE, vol.66, no.8-9, pp.719-723, 2021 (SCI-Expanded)
A series of condensation products were synthesized by treatment of some aryl-substituted 1,2-amino alcohols with various aromatic aldehydes in the catalyst-free medium in ethanol. The amino alcohols bearing NH group give rise to the 1,3-oxazolidines, while their NH2 group holding analogs lead to the formation of Schiff bases. Some advantages of this protocol are a simple work-up procedure, short reaction time, mild conditions, and good to high yields.