The possibilities of synthetic utilization of enantioselective reductions of prochiral ketones catalyzed by 1,2,3-oxazaborolidines are shown on a series of representative pattern reactions. The presented reactions are evaluated from the point of view of reaction conditions, i.e. type and amount of the used catalyst, reduction agent (BH₃.THF, BH₃.SMe₃, catecholborane), solvent (THF, toluene, CH₂Cl₂, i.a.) or activator (simple alcohols or ethanolamine).