474017-59-9

Upstream product

• 76739-66-7 3,4-di-O-acetyl-D-rhamnal 
• 100-51-6 benzyl alcohol 

Downstream Products

• 75810-07-0 Benzyl 2,6-Dideoxy-α-D-arabino-hexopyranoside 
• 474017-85-1 benzyl 3,4-anhydro-2,6-dideoxy-α-D-galactopyranoside 
• 474018-04-7 benzyl 3,4-anhydro-2,6-dideoxy-α-D-allopyranoside 
• 474017-81-7 benzyl 4-O-mesyl-2,6-dideoxy-α-D-glucopyranoside 
• 474017-73-7 benzyl 3-O-(tert-butyldimethylsilyl)-2,6-dideoxy-α-D-glucopyranoside 
• 474017-77-1 (+)-benzyl 3-(O-t-butyldimethylsilyl)-4-(O-mesyl)-2,6-dideoxy-α-D-glucopyranoside 

Relevant academic research and scientific papers

Regiochemical control of the ring opening of 1,2-epoxides by means of chelating processes. Part 17: Synthesis and opening reactions of cis- and trans-oxides derived from (2S,6R)-2-benzyloxy-6-methyl-3,6-dihydro-2H-pyran, (2R,6R)- and (2S,6R)-2-methoxy-6-m

The regiochemical behavior of the title deoxy anhydrosugars, prepared in an enantioselective way starting from methyl α-D-glucopyranoside, was examined in opening reactions, both under standard and chelating conditions. The results clearly indicate the in