Abstract
Novel cage-type cyclophanes, which are constructed with two rigid macrocyclic skeletons, tetraaza[3.3.3.3]paracyclophanes, and four bridging segments composed of β-L-aspartyl-L-aspartyl residues and β-D-aspartyl-D-aspartyl residues individually, were prepared. Chiral host-guest interactions between the hosts and a hydrophobic guest, pamoic acid, were examined by circular dichroism spectroscopy in aqueous media.
Original language | English |
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Pages (from-to) | 1219-1222 |
Number of pages | 4 |
Journal | Tetrahedron Letters |
Volume | 38 |
Issue number | 7 |
DOIs | |
Publication status | Published - Feb 17 1997 |
All Science Journal Classification (ASJC) codes
- Biochemistry
- Drug Discovery
- Organic Chemistry