79083-35-5

Upstream product

• 917-64-6 methyl magnesium iodide 
• 79083-36-6 methyl 5-O-benzyl-β-D-xylofuranoside 
• 56824-29-4 5-O-benzyl-1,2-O-cyclohexylidene-α-D-xylofuranose 
• 100-51-6 benzyl alcohol 
• 67-56-1 methanol 
• 23202-83-7 5-benzyl-1,2-O-isopropylidene-α-D-xylofuranose 
• 79083-41-3 2,3,5-tri-O-benzyl-1-O-methyl-β-D-xylofuranoside 
• 22170-03-2 1,2-O-cyclohexylidene-5-O-tosyl-α-D-xylofuranose 
• 56824-28-3 3,5-anhydro-1,2-O-cyclohexylidene-α-D-xylofuranose 
• 100-44-7 benzyl chloride 
• 22250-06-2 1,2-O-Cyclohexylidene-α-D-xylofuranose 
• 1824-96-0 methyl xylofuranoside 
• 634914-79-7 methyl 3,5-O-benzylidene-α-D-xylofuranoside 

Relevant academic research and scientific papers

Probing the catalytic mechanism of s-ribosylhomocysteinase (LuxS) with catalytic intermediates and substrate analogues

S-Ribosylhomocysteinase (LuxS) cleaves the thioether bond in S-ribosylhomocysteine (SRH) to produce homocysteine (Hcys) and 4,5-dihydroxy-2,3-pentanedione (DPD), the precursor of the type II bacterial quorum sensing molecule (AI-2). The catalytic mechanis

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

The Use of Grignard Reagents in the Synthesis of Carbohydrates. III. The One-way Anomerization of Methyl Glycofuranosides and the Opening of Their Furanose Rings

The anomerization of methyl glycofuranoside derivatives with methylmagnesium iodide or t-butylmagnesium bromide occurred in a one-way manner.For example, methyl 5-O-benzyl-β-D-ribofuranoside (3β) was converted into the corresponding α-anomer (3α) in a 95p