26295-51-2Relevant academic research and scientific papers
Synthesis of α- and β-d-glucopyranosyl triazoles by CuAAC 'click chemistry': reactant tolerance, reaction rate, product structure and glucosidase inhibitory properties
Dedola, Simone,Hughes, David L.,Nepogodiev, Sergey A.,Rejzek, Martin,Field, Robert A.
experimental part, p. 1123 - 1134 (2010/09/12)
CuI-catalysed azide alkyne 1,3-dipolar cycloaddition (CuAAC) 'click chemistry' was used to assemble a library of 21 α-d- and β-d-glucopyranosyl triazoles, which were assessed as potential glycosidase inhibitors. In the course of this work, diff
Synthesis of 1-(d-glucopyranosyl)-1,2,3-triazoles and their evaluation as glycogen phosphorylase inhibitors
Bokor, éva,Docsa, Tibor,Gergely, Pál,Somsák, László
experimental part, p. 1171 - 1180 (2010/05/02)
1-(d-Glucopyranosyl)-1,2,3-triazoles were prepared from per-O-acetylated α- and β-d-glucopyranosyl azides as well as per-O-benzoylated (β-d-gluco-hept-2-ulopyranosylazide)onamide and onic acid methylester by using azide-alkyne cycloaddition catalysed by i
