153264-69-8

Upstream product

• 65434-49-3 3-O-benzyl-1,2-O-isopropylidene-α-D-galactofuranose 
• 10368-86-2 1,2:5,6-di-O-isopropylidene-α-D-galactofuranose 
• 100-39-0 benzyl bromide 
• 65451-98-1 3-O-benzyl-1,2:5,6-di-O-isopropylidene-α-D-galactofuranose 

Downstream Products

• 364372-68-9 3,6-di-O-benzyl-1,2-O-isopropylidene-α-D-galactofuranose 
• 153264-71-2 3-O-benzyl-5-O-benzoyl-1,2-O-isopropylidene-6-deoxy-α-D-galactofuranose 
• 364372-69-0 3,6-di-O-benzyl-1,2-O-isopropylidene-α-L-arabino-hexofuranos-5-ulose 
• 220204-92-2 (5R)-3,6-di-O-benzyl-5-deoxy-5-dimethoxyphosphinyl-1,2-O-isopropylidene-β-L-arabino-hexofuranose 
• 220204-93-3 (5S)-3,6-di-O-benzyl-5-deoxy-5-dimethoxyphosphinyl-1,2-O-isopropylidene-β-L-arabino-hexofuranose 
• 220204-95-5 3,6-di-O-benzyl-5-deoxy-5-dimethoxyphosphinyl-1,2-O-isopropylidene-α-D-galactofuranose 
• 153264-70-1 3-O-benzyl-6-deoxy-1,2-O-isopropylidene-α-D-galactofuranose 

Relevant academic research and scientific papers

Synthesis of 5-deoxy-5-phosphinyl-D-galactopyranose derivatives: New phospha-sugar analogs of D-galactose

The addition reaction of dimethyl phosphonate to 3,6-di-O-benzyl-1,2-O-isopropylidene-α-L-arabino-hexofuranos-5-ulose (11), followed by deoxygenation of 5-hydroxyl group, provided 5-deoxy-5-dimethoxyphosphinyl-D-galactofuranose derivative (13a). Reduction

Aureolic acid antibiotics: Synthesis of the cyclohexenone segment from D-glucose

The cyclohexenone segment which is common to all the aureolic acid group of antibiotics has been synthesised from D-glucose.Two routes have been designed to obtain methyl 3-O-benzyl-6-deoxy-2-O-methyl-D-galactopyranoside.Route-A involves the introduction