294660-36-9

Upstream product

• 14618-80-5 (R)-benzyl glycidol 
• 108-24-7 acetic anhydride 
• 199393-64-1 (2R)-1-(benzyloxy)-3-(3-{[(4-methoxybenzyl)oxy]methyl}-5,6-dihydro-1,4-dithiin-2-yl)propan-2-ol 

Downstream Products

• 294660-38-1 (5R,7R)-7-[(benzyloxy)methyl]-5-methoxy-2,3,7,8-tetrahydro-5H-[1,4]dithiino[2,3-c]pyran 
• 294660-39-2 (5S,7R)-7-[(benzyloxy)methyl]-5-methoxy-2,3,7,8-tetrahydro-5H-[1,4]dithiino[2,3-c]pyran 
• 790667-24-2 (2R,6R)-2-[(benzyloxy)methyl]-6-methoxy-3,6-dihydro-2H-pyran 
• 790667-28-6 (1S,2R,4R,6S)-4-Benzyloxymethyl-2-methoxy-3,7-dioxa-bicyclo[4.1.0]heptane 
• 790667-27-5 (1R,2R,4R,6R)-4-Benzyloxymethyl-2-methoxy-3,7-dioxa-bicyclo[4.1.0]heptane 
• 790667-25-3 methyl 6-O-benzyl-4-deoxy-α-L-lyxo-hexopyranoside 
• 790667-31-1 (2R,3R,4S,6R)-6-Benzyloxymethyl-3-bromo-2-methoxy-tetrahydro-pyran-4-ol 
• 294660-37-0 Acetic acid (R)-1-benzyloxymethyl-2-(3-formyl-5,6-dihydro-[1,4]dithiin-2-yl)-ethyl ester 

Relevant academic research and scientific papers

Synthesis of 4-deoxy-L-(and D-)hexoses from chiral noncarbohydrate building blocks

4-Deoxy-L-hexoses were synthesized starting from our previously reported reagent 1 and (R)-benzyl glycidyl ether, which led in few steps to a substituted dihydropyran 6. The stereocontrolled hydroxylation of the latter afforded the corresponding 4-deoxy-L