69734-25-4

Upstream product

• 20585-18-6 methyl 4,6-dideoxy-α-D-glucopyranoside 
• 98-59-9 p-toluenesulfonyl chloride 
• 4990-82-3 methyl 4,6-dichloro-4,6-dideoxy-α-D-galactopyranoside 

Downstream Products

• 81734-19-2 methyl 2-O-p-tosyl-3-O-benzoyl-4,6-dideoxy-α-D-allopyranoside 
• 87419-07-6 methyl 3-bromo-3,4,6-trideoxy-2-O-p-tosyl-α-D-ribo-hexopyranoside 
• 101155-81-1 methyl 2-O-p-toluenesulfonyl-4,6-dideoxy-α-D-ribo-hexopyranoside 

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

PREPARATION OF O-1 - C-6 AND O-7 - C-14 FRAGMENTS OF COLLETODIOL

(5S,2E)-5-Tetrahydropyranyloxy-2-hexenoic acid and p-toluenesulfonylethyl (4R,5R,7R,2E)-7-hydroxy-4,5-dimethylmethylenedioxy-2-octenoate were prepared from ethyl acetoacetate and D-glucose, respectively.