79083-35-5

Upstream product

• 634914-79-7 methyl 3,5-O-benzylidene-α-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 
• 79083-36-6 methyl 5-O-benzyl-β-D-xylofuranoside 
• 917-64-6 methyl magnesium iodide 

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

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

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