169873-66-9

Upstream product

• 651736-08-2 methyl 4,6-O-benzylidene-α-D-arabino-hexopyranoside-2-ulose Z-oxime 
• 128657-58-9 methyl 2-amino-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 857489-45-3 methyl 2-dibenzylamino-3-O-tert-butyldimethylsilyl-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 651735-96-5 methyl 2-N,N-dibenzylamino-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 857489-46-4 methyl 2-benzylamino-3-O-tert-butyldimethylsilyl-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 651735-94-3 methyl 2-N-benzylamino-3-O-trimethylsilyl-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 

Downstream Products

• 651736-02-6 methyl 2-N-benzylamino-4,6-O-benzylidene-2-deoxy-α-D-ribohexopyranoside-3-ulose 

Relevant academic research and scientific papers

A tuneable method for N-debenzylation of benzylamino alcohols

(Chemical Equation Presented) N-lodosuccinmide provides a mild, convenient, and tuneable reagent for the selective mono- or didebenzylation in representative, multifunctionalized carbohydrate and amino acid derived N-dibenzylamines with neighboring O-func

Precise structure activity relationships in asymmetric catalysis using carbohydrate scaffolds to allow ready fine tuning: dialkylzinc-aldehyde additions.

The ready construction of 24 stereochemically and functionally diverse carbohydrate ligand structures from a core D-glucosamine scaffold has allowed the evaluation of broad ranging structure activity relationships in ligand accelerated zincate additions t