| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5231330 | Tetrahedron | 2005 | 6 Pages |
Abstract
The synthesis of a mono-galactosylated amphiphilic β-cyclodextrin, in five steps from mono-6-azido-6-deoxy-β-cyclodextrin, via coupling to a N-β-d-galactopyranosylamino-antenna is described. Both characterization by electrospray mass spectrometry and NMR show the presence of only the mono-substituted product. The Langmuir isotherms of the final product and intermediates are described.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Alain Salameh, Adina N. Lazar, Anthony W. Coleman, Hélène Parrot-Lopez,