I. Suzuki et al., Difference in orientation of a guest within a cavity of beta-cyclodextrinsbearing an N-acetylaminoacyl group, HETEROCYCLE, 52(2), 2000, pp. 567-570
H-1-NMR studies revealed that either the benzene or the naphthalene ring of
8-anilinonaphthalene-1-sulfonate (ANS) was accommodated by beta-cyclodextr
in (beta-CyD) bearing an N-Ac-L-Leu residue, while beta-CyDs bearing an N-A
c-L-Ile and N-Ac-L-Val residues accommodated the naphthalene ring of ANS.