215727-95-0Relevant academic research and scientific papers
Synthesis of chiral carbohydrate-centered dendrimers
Dubber, Michael,Lindhorst, Thisbe K.
, p. 1265 - 1266 (1998)
D-Glucose was converted into its per-O-(2-aminoethyl)-functionalized derivative 4, which served as initiator core for the construction of the chiral, monodisperse PAMAM-type carbohydrate-centered hybrid dendrimer 7.
Synthesis of octopus glycosides: Core molecules for the construction of glycoclusters and carbohydrate-centered dendrimers
Dubber, Michael,Lindhorst, Thisbe K.
, p. 35 - 41 (1998)
Allyl α-D-glucopyranoside was perallylated to allyl 2,3,4,6-tetra-O-allyl-α-D-glucopyranoside and this was converted into an array of uniformly functionalized spacer glycosides of an 'octopus' type, taking advantage of the rich chemistry of the allyl ethe
Octopus glycosides: Multivalent molecular platforms for testing carbohydrate recognition and bacterial adhesion
Lindhorst, Thisbe K.,Dubber, Michael
, p. 90 - 97 (2015)
Multivalency of carbohydrate-protein interactions is critical for cell adhesion, including attachment of bacteria to their host cells. To investigate specific parameters of multivalency effects, a variety of multivalent glycoconjugates has been designed a
