Synthesis of New Carnosine Derivatives of β-Cyclodextrin and Their Hydroxyl Radical Scavenger Ability
✍ Scribed by Diego La Mendola; Salvatore Sortino; Graziella Vecchio; Enrico Rizzarelli
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- German
- Weight
- 186 KB
- Volume
- 85
- Category
- Article
- ISSN
- 0018-019X
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In order to examine the molecular recognition effect of a three-dimensional hydrophobic cavity, seven β-cyclodextrin derivatives (1-7) bearing hydrophobic substituents on the primary side, and three structurally related calixarene derivatives (8-10) were synthesized and used as coating materials for
The synthesis of a new water-soluble semi-rotaxane monomer consisting of threaded 2,6-dimethyl-P-cyclodextrin on a 3-O-( 11 -acryloylaminoundecanoyl)cholic acid guest component is described. This new monomer complex was polymerized in water as a solvent in the presence of a free radical redox initia