Xm. Zhu et al., Determination of the absolute configuration of methyl group in the acyl moiety of quillajasaponins, ACT CHIM S, 59(10), 2001, pp. 1653-1659
Two diastereoisomers of the Cg lactone, (3S, 5S, 6S) - 3, 5 - dihydroxy - 6
- methyl - delta - octanolide and (3S, 5S, 6R) - 3, 5 - dihydroxy - 6 - me
thyl - delta - octanolide, have been enantioselectively synthesized and com
pared with the natural sample, thereby determining the absolute configurati
on of the methyl group in the acyl moiety of quillajasaponins to be S.