T. Yamazaki et al., DIASTEREOSPECIFIC CYCLIZATION OF OPTICALLY-ACTIVE TRIFLUOROMETHYLATEDEPOXYCARBAMATES, Tetrahedron : asymmetry, 5(9), 1994, pp. 1823-1830
Optically active trifluoromethylated propargylic alcohol was prepared
by enzymatic asymmetric hydrolysis and was transformed into chiral ami
noalcohol derivatives in a diastereospecific fashion, whose results we
re qualitatively supported by semiempirical molecular orbital calculat
ions.