211232-97-2

Upstream product

• 20031-21-4 1,2-O-isopropylidene-α-D-xylose 
• 42854-94-4 5-bromo-5-deoxy-1,2-O-isopropylidene-α-D-xylofuranose 
• 4152-79-8 1,2-O-isopropylidene-5-methyl-5-deoxy-α-D-xylofuranose 

Downstream Products

• 79698-11-6 2,5-anhydro-1-benzyloxycarbonylamino-1,6-dideoxy-3,4-di-O-(methylsulfonyl)-D-iditol 
• 79698-11-6 2,5-anhydro-1-benzyloxycarbonylamino-1,6-dideoxy-3,4-di-O-(methylsulfonyl)-D-gulitol 
• 79698-10-5 2,5-anhydro-1-benzyloxycarbonylamino-1,6-dideoxy-D-iditol 
• 79698-10-5 2,5-anhydro-1-benzyloxycarbonylamino-1,6-dideoxy-D-gulitol 
• 79698-09-2 (2S,3R,4R,5R)-2-Aminomethyl-5-methyl-tetrahydro-furan-3,4-diol 

Relevant academic research and scientific papers

Binding and catalysis by yeast aldose reductase: A substrate-analog approach with new aldose derivatives

5-Deoxy-D-xylofuranose derivatives and a range of new 5,6-dideoxy analogs of D-glucofuranose bearing azido or fluoro substituents were synthesised and employed as substrates of the NADH-dependent aldehyde reduction catalysed by yeast aldose reductase. In

DIRECT FORMATION OF C-GLYCOFURANOSYL DERIVATIVES BY THE REACTION OF D-ALDOSES WITH NITROMETHANE AND METHYL NITROACETATE

Under appropriate conditions, condensation of D-ribose (1) with nitromethane afforded D-ribofuranosylnitromethanes (3 and 4) directly, in high yields.On the other hand, similar reactions of 5-deoxy-D-xylose (9) gave acyclic products (11), which were readi