80229-16-9

Upstream product

• 100-44-7 benzyl chloride 
• 100-39-0 benzyl bromide 
• 634914-79-7 methyl 3,5-O-benzylidene-α-D-xylofuranoside 
• 634914-80-0 methyl 2-O-benzyl-3,5-O-benzylidene-α-D-xylofuranoside 

Downstream Products

• 119690-13-0 methyl 2,5-di-O-benzyl-α-D-erythro-pentofuranosid-3-ulose 
• 119690-17-4 methyl 3-O-acetyl-2,5-di-O-benzyl-3-C-(p-nitrophenylazo)-α-D-xylofuranoside 
• 119690-17-4 methyl 3-O-acetyl-2,5-di-O-benzyl-3-C-(p-nitrophenylazo)-α-D-ribofuranoside 
• 119690-21-0 (2R,3R,4R,5S)-4-Benzyloxy-2-benzyloxymethyl-5-methoxy-3-(4-nitro-phenylazo)-tetrahydro-furan-3-ol 
• 119690-21-0 (2R,3S,4R,5S)-4-Benzyloxy-2-benzyloxymethyl-5-methoxy-3-(4-nitro-phenylazo)-tetrahydro-furan-3-ol 
• 119720-38-6 methyl 2,5-di-O-benzyl-α-D-erythro-pentofuranosid-3-ulose 4-nirtrophynylhydrazone 

Relevant academic research and scientific papers

Studies on the regioselective reductive ringcleavage reactions of 3,5-O-arylidene-D-xylofuranosides

Reductive ring cleavage of 3,5-O-arylidene-D-xylofuranosides using LiAlH4-AlCl3 and NaBH3CN-BF3 proceeded regioselectively to provide secondary alcohol as the major product. The effect of the substitutents on th

HYDROGENOLYSIS OF 3,5-O-BENZYLIDENE ACETALS WITH THE LiAlH4-AlCl3 REAGENT IN METHYL D-XYLOFURANOSIDES

The hydrogenolysis of methyl 3,5-O-benzylidene-α- and -β-D-xylofuranoside derivatives with the LiAlH4-AlCl3 reagent gave 5-benzyl ethers as main products.In some cases the attack of the reagent occured at the ring oxygen of the furanoside skeleton to yiel