Ei. Fukusaki et al., Lipase-catalyzed kinetic resolution of 2,3-epoxy-1-tridecanol and its application to facile synthesis of (+)-Disparlure, J BIOSCI BI, 87(1), 1999, pp. 103-104
Acylation of (+/-)-2,3-epoxy-1-tridecanol with acetic anhydride in diisopro
pyl ether by porcine pancreatic lipase yielded (2R, 3S)-2,3-epoxy-1-trideca
nol as the remaining substrate with an optical purity of over 99% ee. (+)-D
isparlure was synthesized in two steps from this optically active epoxy alc
ohol.