H. Akita et al., LIPASE-CATALYZED RESOLUTION OF (+ -)-2-SUBSTITUTED 1-PROPANOL DERIVATIVES POSSESSING AN AROMATIC RING/, Biocatalysis, 9(1-4), 1994, pp. 79-87
For the purpose of the chiral synthesis of natural products, lipase-ca
talyzed kinetic resolutions of three types of 2-substituted 1-propanol
derivatives (each having an aromatic ring) was investigated. In every
case, chiral recognition of the primary alcohol unit took place to pr
ovide the corresponding alcohols and the acetates in high optical puri
ty. The (2S,3S)-5-aryl-2-methyl-3-hydroxy-4E-pentenol 5 was formally c
onverted into the antibiotic, (-)-oudemansin X.