Clicking Sugars onto Sugars: Oligosaccharide Analogs and Glycoclusters on Carbohydrate Scaffolds
We review herein the recent applications of the copper(I)-catalyzed azide-alkyne cycloaddition to couple carbohydrates and produce compounds of various architectures, molecular weights, and biological properties. The different parts of the chapter correspond to the nature of the products, limited to...
Guardado en:
Autores principales: | Uhrig, M.L., Kovensky, J. |
---|---|
Formato: | CHAP |
Materias: | |
Acceso en línea: | http://hdl.handle.net/20.500.12110/paper_97811182_v_n_p107_Uhrig |
Aporte de: |
Ejemplares similares
-
Clicking Sugars onto Sugars: Oligosaccharide Analogs and Glycoclusters on Carbohydrate Scaffolds
por: Uhrig, María Laura, et al.
Publicado: (2013) -
Synthesis of divalent ligands of β-thio- And β-N-galactopyranosides and related lactosides and their evaluation as substrates and inhibitors of Trypanosoma cruzi trans-sialidase
por: Cano, M.E., et al. -
Synthesis of divalent ligands of β-thio- And β-N-galactopyranosides and related lactosides and their evaluation as substrates and inhibitors of Trypanosoma cruzi trans-sialidase
Publicado: (2014) -
Efficient synthesis of thiolactoside glycoclusters by ruthenium-catalyzed cycloaddition reaction of disubstituted alkynes on carbohydrate scaffolds
por: Cagnoni, A.J., et al. -
Genetics and breeding of sugar beet
Publicado: (2005)