Development of a family of beta-amino alcohol ligands with two stereocenters for highly efficient enantioselective trimethylsilylcyanation of aldehydes
Js. You et al., Development of a family of beta-amino alcohol ligands with two stereocenters for highly efficient enantioselective trimethylsilylcyanation of aldehydes, CHEM COMMUN, (19), 2000, pp. 1963-1964
The asymmetric addition of Me3SiCN to aldehydes catalyzed by titanium(iv) c
omplexes of N-sulfonylated derivatives of beta-amino alcohols gave excellen
t ee's up to 96% ee.