81625-96-9

Upstream product

• 35905-39-6 benzyl 2,3-anhydro-4,6-O-benzylidene-α-D-allopyranoside 
• 104875-44-7 3-azido-3-deoxy-D-glucopyranose 
• 13964-23-3 3-azido-3-deoxy-1,2:5,6-di-O-propan-2-ylidene-α-D-allofuranose 
• 1125-88-8 benzaldehyde dimethyl acetal 

Downstream Products

• 104875-47-0 benzyl 3-azido-4,6-O-benzylidene-3-deoxy-2-O-<(trifluoromethyl)sulfonyl>-α-D-glucopyranoside 
• 72869-08-0 benzyl 3-amino-4,6-O-benzylidene-3-deoxy-α-D-glucopyranoside 
• 104875-48-1 benzyl 3-azido-4,6-O-benzylidene-2,3-dideoxy-2-fluoro-α-D-mannopyranoside 
• 81625-98-1 benzyl 3-azido-4,6-O-benzylidene-3-deoxy-2-O-(methylsulfonyl)-α-D-glucopyranoside 
• 81626-02-0 N-((4aR,6S,7R,8R,8aS)-6-Benzyloxy-7-hydroxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yl)-acetamide 

Relevant academic research and scientific papers

Chiral Synthons for the Total Synthesis of Fluoro Amino Acids and Fluoro Analogues of Antibiotic Sugars

Configurationally different 3-azido-2,3-dideoxy-2-fluoro and 2-azido-2,3-dideoxy-3-fluoro sugars, synthetic precursors of biologically important fluoro amino acids, were synthesized.Axial alcohols involved in vicinal diaxial systems undergo fluorodehydrox

Synthesis of Amino Sugars from Tri-O-acetyl-D-glucal via Epoxides

Simultaneous stereospecific trans addition of the benzyloxy and bromo residues with N-bromosuccinimide in benzyl alcohol to tri-O-acetyl-D-glucal (3,4,6-tri-O-acetyl-1,2-dideoxy-D-arabino-1-hexenopyranose; 1) gave a mixture of benzyl 3,4,6-tri-O-acetyl-2-