1393360-75-2

Upstream product

• 582-52-5 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 18685-18-2 3-O-benzyl-1,2-5,6-O-diisopropylidene-α-D-glucofuranose 
• 100-39-0 benzyl bromide 
• 65877-63-6 3-O-benzyl-D-glucopyranose 
• 617-86-7 triethylsilane 
• 201230-82-2 carbon monoxide 
• 1404561-47-2 3-O-benzyl-1,2-O-diacetyl-4,6-O-p-methoxybenzylidene-D-glucopyranose 

Downstream Products

• 1393360-76-3 3-O-acetyl-2,6-anhydro-4-O-benzyl-5,7-O-p-methoxybenzylidene-D-glycero-D-gulo-heptitol 
• 1393360-77-4 1-O-acetyl-2,6-anhydro-4-O-benzyl-5,7-O-p-methoxybenzylidene-D-glycero-D-gulo-heptitol 
• 1393360-78-5 3-O-acetyl-2,6-anhydro-4-O-benzyl-5,7-O-p-methoxybenzylidene-1-O-tert-butyldiphenylsilyl-D-glycero-D-gulo-heptitol 
• 1393360-79-6 1-O-acetyl-2,6-anhydro-4-O-benzyl-5,7-O-p-methoxybenzylidene-3-O-tert-butyldiphenylsilyl-D-glycero-D-gulo-heptitol 
• 1393360-80-9 1-O-acetyl-2,6-anhydro-4-O-benzyl-5-O-p-methoxybenzyl-3-O-tert-butyldiphenylsilyl-D-glycero-D-gulo-heptitol 
• 1393360-81-0 3-O-acetyl-2,6-anhydro-4-O-benzyl-5-O-p-methoxybenzyl-1-O-tert-butyldiphenylsilyl-D-glycero-D-gulo-heptitol 
• 1393360-85-4 3-O-benzyl-1,6-O-diacetyl-2-O-(p-methoxybenzyl)-4-O-tert-butyldiphenylsilyl-α-L-glucopyranose 
• 1393360-84-3 3-O-benzyl-1,6-O-diacetyl-2-O-(p-methoxybenzyl)-4-O-tert-butyldiphenylsilyl-β-L-glucopyranose 
• 1393360-86-5 3-O-benzyl-1,6-O-diacetyl-4-O-tert-butyldiphenylsilyl-β-L-glucopyranose 
• 1393360-87-6 3-O-benzyl-2,6-O-diacetyl-4-O-tert-butyldiphenylsilyl-α-L-mannopyranose 
• 1393360-88-7 3-O-benzyl-1,6-O-diacetyl-2-O-(p-methoxybenzyl)-β-L-glucopyranose 
• 1393360-89-8 3-O-benzyl-1,6-O-diacetyl-2-O-(p-methoxybenzyl)-β-L-galactopyranose 
• 1393360-90-1 3-O-benzyl-1,4-O-diacetyl-2-O-(p-methoxybenzyl)-β-L-galactopyranose 

Relevant academic research and scientific papers

Synthesis of orthogonally protected l-glucose, l-mannose, and l-galactose from d-glucose

An efficient route to orthogonally protected l-glucose, l-mannose, and l-galactose is described. Using the strategy to switch the functional groups at C1 and C5 of d-glucose, l-glucose is obtained via a key intermediate C-glycoside. Preparations of l-mannose and l-galactose derivatives from the orthogonally protected l-glucose were accomplished in good yields using the Lattrell-Dax method.