110889-41-3

Upstream product

• 110889-23-1 methyl 2-O-benzoyl-4,6-O-benzylidene-3-C-(ethoxycarbonylmethylene)-α-D-ribo-hexopyranoside 
• 110889-25-3 methyl 2,2¹-di-O-acetyl-4,6-O-benzylidene-3-C-<(z)-2-hydroxyethylidene>-α-D-ribo-hexopyranoside 
• 110889-24-2 (4aR,6S,7R,8aS)-8-[2-Hydroxy-eth-(E)-ylidene]-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-ol 
• 110889-38-8 methyl 2,2¹-di-O-acetyl-4,6-O-benzylidene-3-C-<(R)-1,2-dihydroxyethyl>-α-D-glucopyranoside 
• 110889-39-9 (4aR,6S,7R,8R,8aR)-8-((R)-1,2-Dihydroxy-ethyl)-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine-7,8-diol 
• 28642-65-1 methyl 2-O-benzoyl-4,6-O-benzylidene-α-D-ribo-hexopyranosid-3-ulose 
• 108-24-7 acetic anhydride 
• 110889-40-2 methyl 2,2¹-anhydro-4,6-O-benzylidene-3-C-<(R)-1,2-dihydroxyethyl>-α-D-glucopyranoside 

Relevant academic research and scientific papers

SYTHESIS OF METHYL 4-DEOXY-3-C--α-D-xylo-HEXOPYRANOSIDE AND METHYL 2,21-ANHYDRO-3-C--α-D-GLUCOPYRANOSIDE DERIVATIVES

The title branched-chain sugars possessing a new type of two-carbon branch were synthesised from D-glucose.These compounds are important intermediates for a total synthesis of the nucleoside antibiotics, amipurimycin and miharamycin.