28541-77-7

Upstream product

• 106-41-2 4-bromo-phenol 
• 66888-27-5 penta-O-acetyl-D-mannose 
• 530-26-7 D-Mannose 
• 83-87-4 D-Mannose pentaacetate 
• 28619-28-5 4-bromophenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside 
• 3046-26-2 p-bromophenol, potassium salt 
• 53958-21-7 4,6-di-O-acetyl-2,3-O-carbonyl-α-D-mannopyranosyl bromide 
• 187269-63-2 2,3,4,6-tetra-O-pivaloyl-α-D-mannopyranosyl fluoride 
• 2713-54-4 α-D-mannopyranosyl fluoride 
• 243120-93-6 4-bromophenyl tetra-O-pivaloyl-α-D-mannopyranoside 
• 120489-17-0 Acetic acid (3aS,4R,6R,7R,7aS)-6-acetoxymethyl-4-(4-bromo-phenoxy)-2-oxo-tetrahydro-[1,3]dioxolo[4,5-c]pyran-7-yl ester 
• 2823-44-1 2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl fluoride 

Relevant academic research and scientific papers

Preparation and characterization of glycopolymers with biphenyl spacers: Via Suzuki coupling reaction

Poly(vinylbiphenyl)s bearing glycoside ligands at the side chains were prepared using the Suzuku coupling reaction. Effects of glycoside reactant concentration, halide species, glycoside species, and catalyst species on the incorporation of glycoside ligand into the polymer were investigated. The obtained glycopolymers exhibited specific binding to proteins corresponding to the glycoside ligands. In addition, the biphenyl spacers formed by the Suzuki coupling reaction in the glycopolymer were fluorescent, whereas the polymer precursor was not.

COMPOUNDS AND METHODS FOR TREATING BACTERIAL INFECTIONS

The present invention encompasses compounds and methods for treating urinary tract infections.

Stereospecific α-D-mannosylation

The stereospecific formation of α-D-mannosyl glycosidic linkages has been achieved in high yield using tetra-O-pivaloyl-α-D-mannopyranosyl fluoride and boron trifluoride diethyl etherate in dichloromethane. Examples of the α-D-mannosylation of primary, secondary, benzylic and phenolic hydroxyl groups are described. Copyright (C) 1999 Elsevier Science Ltd.