Supramolecular Chemistry for Nanosciences
Supramolecular Chemistry for Nanosciences
Supramolecular Chemistry for Nanosciences
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Cyclodextrins<br />
HO<br />
O<br />
O<br />
HO<br />
O<br />
HO<br />
OH<br />
HO<br />
O HO<br />
OH<br />
OH<br />
O<br />
HO<br />
O<br />
O<br />
OH<br />
O<br />
Lipophilic<br />
cavity<br />
HO<br />
HO<br />
OH<br />
O<br />
OH<br />
n<br />
Hydrophilic<br />
periphery<br />
Medical applications<br />
HO<br />
OH<br />
O<br />
OH<br />
O<br />
O<br />
OH<br />
=<br />
N<br />
H 3 C<br />
H<br />
N<br />
O<br />
O<br />
H 2 N<br />
O<br />
S<br />
OH<br />
H<br />
N<br />
O<br />
O<br />
N<br />
O<br />
N<br />
N<br />
NH<br />
O<br />
NH 2<br />
N<br />
N<br />
N<br />
H 2 N<br />
O<br />
HN<br />
O<br />
Solubilization of<br />
organic compounds<br />
R. Breslow, Acc. Chem. Res. 1995, 28, 146<br />
Y. Fukazawa et al., Tetrahedron. Lett., 2001, 42, 3203<br />
(drugs…) in water J. T. Rademacher, C. Czarnick, JACS, 1993, 3018<br />
04/03/2008 M1-<strong>Nanosciences</strong><br />
10
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