Y. Bahaddi et al., ENANTIOMERIC DISCRIMINATION IN SOLID-STATE CYCLODEXTRIN COMPLEXES, Bulletin de la Societe chimique de France, 132(3), 1995, pp. 330-332
Cyclodextrins were used to prepare inclusion complexes of a volatile c
hiral compound, 1,7-dioxaspiro[5.5]undecane 1, a pheromone of Dacus ol
eae. The included pheromone was recovered from the inclusion complexes
. Cyclodextrins that were unsymmetrically substituted with at least on
e unit different from the others could form inclusion complexes prefer
entially with the S enantiomer of the pheromone.