344779-62-0

Upstream product

• 98-88-4 benzoyl chloride 
• 77987-49-6 benzyl 2-hydroxyethylcarbamate 
• 344779-61-9 C₄₀H₃₃NO₁₁ 
• 165877-99-6 2,3,4,6-tetra-O-Bz-β-D-glucopyranosyl bromide 

Downstream Products

• 195863-89-9 2-aminoethyl 2,3,4,6-tetra-O-benzoyl-β-D-glucopyranoside 
• 123126-70-5 2-(benzyloxycarbonyl)aminoethyl β-D-glucopyranoside 

Relevant academic research and scientific papers

Design, modeling and synthesis of functionalized paromamine analogs

Based on the published NMR structure of the antibiotic paromomycin complexed with the A-site of Escherichia coli 16S ribosomal RNA, a set of C-5 functionalized analogs of paromamine was designed and synthesized, incorporating cyclic and acyclic appendages and terminating with one or more ammonium groups.

Self-assembly of a water-soluble [2]rotaxane with carbohydrate stoppers

A [2]rotaxane self-assembles spontaneously by 'slippage' in D2O during one week at room temperature when a dumbbell-shaped compound, containing a hydroquinone ring recognition site and terminated by P-D-glucopyranose units, is mixed with cyclobis(paraquat-p-phenylene) tetrachloride. A [2]rotaxane with benzoylated D-glucopyranose residues is obtained when the dumbbell-shaped octabenzoate serves as a template for the formation of the cyclobis(paraquat-p-phenylene) tetracation in DMF.

Synthesis of carbohydrate-containing dendrimers. 5. Preparation of dendrimers using unprotected carbohydrates

Carbohydrate-containing dendrimers have been prepared using completely unprotected carbohydrates employing a convergent growth approach. The facile syntheses of lower generation dendrimers, using the amide bond forming methodology, opens up the possibilit