92122-96-8

Upstream product

• 67-56-1 methanol 
• 132884-64-1 1,2-anhydro-3,4-di-O-benzyl-β-L-arabinopyranose 
• 14260-02-7 3,4-Di-O-acetyl-1,2-O-(1-methoxyethylidene)-β-L-arabinopyranose 
• 75247-31-3 α-1-bromo-1-deoxy-2,3,4-tri-O-acetyl-L-arabinopyranose 
• 92122-94-6 3,4-Di-O-benzyl-1,2-O-(1-methoxyethilidene)-β-L-arabinopyranose 
• 158468-64-5 2-O-acetyl-3,4-di-O-benzyl-β-L-arabinopyranosyl chloride 
• 158468-65-6 2-O-acetyl-3,4-di-O-benzyl-α-L-arabinopyranosyl fluoride 
• 92122-95-7 Methyl 2-O-acetyl-3,4-di-O-benzyl-α-L-arabinopyranoside 

Downstream Products

• 92122-97-9 Methyl 2-O-(2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-3,4-di-O-benzyl-α-L-arabinopyranoside 

Relevant academic research and scientific papers

SYNTHESIS, CONFORMATIONAL ANALYSIS, AND THE GLYCOSIDIC COUPLING REACTION OF SUBSTITUTED 2,7-DIOXABICYCLOHEPTANES: 1,2-ANHYDRO-3,4-DI-O-BENZYL-β-L-ARABINOPYRANOSE

The title 1,2-anhydro sugar (8) was synthesized from L-arabinose.The key intermediate for the syntesis was 2-O-acetyl-3,4-di-O-benzyl-α-L-arabinopyranosyl fluoride (7) which was transformed into the target compound by ring closure with potassium tert-buto