Diverse Motifs of Mannoside Clustering on a β-Cyclodextrin Core
✍ Scribed by Ortega-Caballero, Fernando; Giménez-Martínez, Juan J.; Vargas-Berenguel, Antonio
- Book ID
- 115520392
- Publisher
- American Chemical Society
- Year
- 2003
- Tongue
- English
- Weight
- 121 KB
- Volume
- 5
- Category
- Article
- ISSN
- 1523-7060
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📜 SIMILAR VOLUMES
A convenient method for the synthesis of b-d-gluco-, b-d-galacto-, 2-acetamido-2-deoxy-b-d-gluco-and ad-mannopyranosylamine clusters based on cyclomaltoheptaose (b-cyclodextrin) is presented. The synthesis involves: 1) the one-pot synthesis of the acetylated chloroacetyl N-glycoside derivatives of d
The synthesis of three first-order dendrimers based on a b-cyclodextrin core containing fourteen Val, Phe and Val-Phe residues is described. The guest binding ability of the tetradecavalent peptidyl b-cyclodextrin derivative has been tested by calorimetric titration and the thermodynamic parameters
A selective, versatile, robust methodology for bifunctionalization of b-cyclodextrin is achieved allowing the attachment of peptides in varying C-and/or N-terminal combinations on resin using Fmoc SPPS. Two linkers are attached to cyclodextrin enabling selective binding to the resin (or a peptide at