127875-10-9

Upstream product

• 135041-31-5 methyl 3-O-allyl-2,4-di-O-benzyl-α-L-rhamnopyranoside 
• 114219-31-7 (2S,3R,4S,5S,6R)-3,5-Bis-benzyloxy-2-methoxy-6-methyl-tetrahydro-pyran-4-ol 
• 106-95-6 allyl bromide 
• 134311-55-0 Methyl 3-O-allyl-2,4-di-O-benzyl-6-deoxy-α-D-glucopyranoside 
• 100-39-0 benzyl bromide 
• 69558-09-4 methyl 3-O-allyl-4-O-benzyl-α-L-rhamnopyranoside 
• 142967-66-6 Methyl 3-O-allyl-2,4-di-O-benzyl-6-O-p-tolylsulfonyl-α-D-glucopyranoside 
• 142967-65-5 Methyl 3-O-allyl-2-O-benzyl-6-O-p-tolylsulfonyl-α-D-glucopyranoside 
• 58341-56-3 Methyl 3-O-allyl-2-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside 
• 142967-67-7 Methyl 3-O-allyl-2,4-di-O-benzyl-6-deoxy-6-iodo-α-D-glucopyranoside 
• 58341-60-9 Methyl 3-O-allyl-2,4-di-O-benzyl-α-D-glucopyranoside 
• 58341-57-4 Methyl 3-O-allyl-2-O-benzyl-α-D-glucopyranoside 
• 15038-71-8 methyl 2-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside 
• 6619-09-6 methyl 6-O-tosyl-α-D-glucopyranoside 

Downstream Products

• 138552-38-2 Acetic acid (2S,3R,4R,5S,6S)-4-allyloxy-3,5-bis-benzyloxy-6-methyl-tetrahydro-pyran-2-yl ester 
• 114283-90-8 1,3-Di-O-acetyl-2,4-di-O-benzyl-6-deoxy-α,β-D-glucopyranose 
• 141942-25-8 1,3-Anhydro-2,4-di-O-benzyl-β-D-glucopyranose 
• 134311-58-3 3-O-Acetyl-2,4-di-O-benzyl-6-deoxy-α-D-glucopyranosyl chloride 
• 42822-31-1 2,4-Di-O-benzyl-6-deoxy-α,β-D-glucopyranose 
• 138579-53-0 C₇₆H₉₀O₁₇ 
• 138552-39-3 C₄₄H₅₂O₉ 
• 138552-40-6 (2S,3R,4R,5R,6S)-3,5-Bis-benzyloxy-2-((2R,3R,4R,5R,6S)-4,5-bis-benzyloxy-2-methoxy-6-methyl-tetrahydro-pyran-3-yloxy)-6-methyl-tetrahydro-pyran-4-ol 

Relevant academic research and scientific papers

Synthesis and conformational analysis of substituted 2,6-dioxabicycloheptanes: 1,3-anhydro-2,4-di-O-benzyl-6-deoxy-β-D-glucopyranose by 1H-NMR spectroscopy and molecular mechanics calculation

A highly selective ring opening reduction of methyl 3-O-allyl-2-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside provided the 2,4-di-O-benzyl derivative.This was toluenesulfonylated or iodinated and subsequently reduced to give crystalline methyl 3-O-allyl-

A stereoconvergent synthesis of the oligosaccharide segment of glycopeptidolipid antigen of mycobacterium avium serotype 4 : A dominant serovariant observed in patients with acquired immune deficiency syndrome

A stereoconvergent approach for the oligosaccharide segment of glycopeptidolipid antigen of Mycobacterium avium serotype 4, commonly occurs in AIDS patients, is described. A stereoconvergent approach to the tetrasaccharide segment of Mycobacterium avium serotype 4 is described. 4-O-Me-α-L-Rhap-(1→4)-2-O-Me-α-L-Fucp-(1→3)-a-L-Rhap- (1→2)-6-deoxy-L-Talose.

Partially Benzylated Derivatives of 6-Deoxy-D-glucose

Several partially benzylated derivatives of 6-deoxy-D-glucose (D-quinovose) were synthesized from appropriate di-O-benzyl-D-glucosides whose primary hydroxyl group is unprotected, via unimolar tosylation and subsequent reduction with LiAlH4.