Abstract
A series of asymmetric phenylacetylene tridendrons is prepared by coupling polar monodendrons having t-butyl esters on their periphery with a non-polar monodendron having t-butyl groups on its periphery. Subsequent conversion of the t-butyl esters to carboxylic acids by thermolysis gives amphiphilic dendrimers having polar domains of various size. The characterization and solution phase behavior of these structures is discussed.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 15331-15347 |
| Number of pages | 17 |
| Journal | Tetrahedron |
| Volume | 53 |
| Issue number | 45 |
| DOIs | |
| State | Published - Nov 10 1997 |
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry