Abstract
D - Arabinose was converted into new allylic furanosyl and pyranosyl glycosides by applying two different reaction conditions. The glycosides then were treated with sodium azide to get triazoline compounds via a 1,3-dipolar cycloaddition. The new glycosides and the triazoline compounds were identified by I.R, H-1 - and C-13 - N.M.R. spectroscopy.