A series of enantiopure aminoalcohols were synthesized from the corres
ponding diols by activation of the diols as cyclic carbonates, azide o
pening of the carbonates, and hydrogenation of the resulting azidoalco
hols. Factors affecting the azide opening of the carbonates, a simple
workup procedure, and a large scale synthesis of (1R,2S)-(-)-2-amino-1
,2-diphenylethanol are described. (C) 1996 Elsevier Science Ltd.