80229-18-1

Upstream product

• 80229-11-4 methyl 2-O-benzyl-3,5-O-benzylidene-β-D-xylofuranoside 
• 51587-94-1 methyl 3,5-O-benzylidene-β-D-xylofuranoside 
• 100-44-7 benzyl chloride 

Downstream Products

• 119690-13-0 methyl 2,5-di-O-benzyl-β-D-erythro-pentofuranosid-3-ulose 
• 119690-17-4 methyl 3-O-acetyl-2,5-di-O-benzyl-3-C-(p-nitrophenylazo)-β-D-xylofuranoside 
• 119690-17-4 methyl 3-O-acetyl-2,5-di-O-benzyl-3-C-(p-nitrophenylazo)-β-D-ribofuranoside 
• 119690-21-0 (2R,3R,4R,5R)-4-Benzyloxy-2-benzyloxymethyl-5-methoxy-3-(4-nitro-phenylazo)-tetrahydro-furan-3-ol 
• 119690-21-0 (2R,3S,4R,5R)-4-Benzyloxy-2-benzyloxymethyl-5-methoxy-3-(4-nitro-phenylazo)-tetrahydro-furan-3-ol 
• 119690-15-2 methyl 2,5-di-O-benzyl-β-D-erythro-pentofuranosid-3-ulose 4-nirtrophynylhydrazone 

Relevant academic research and scientific papers

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