178319-10-3

Upstream product

• 178319-02-3 allyl 2,6-di-O-benzyl-3-O-p-methoxybenzyl-α-D-galactopyranoside 
• 824-94-2 p-methoxybenzyl chloride 
• 37111-91-4 allyl 2,6-di-O-benzyl-α-D-galactopyranoside 

Downstream Products

• 178319-07-8 allyl 3,4-di-O-acetyl-2,6-di-O-benzyl-α-D-glucopyranoside 
• 178319-08-9 (Z)-prop-1'-enyl 2,6-di-O-benzyl-α-D-glucopyranoside 
• 169822-03-1 allyl 2,6-di-O-benzyl-α-D-glucopyranoside 
• 139684-64-3 (Z)-prop-1'-enyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranoside 
• 6564-72-3 2,3,4,6-tetra-O-benzyl-D-glucopyranose 
• 178319-05-6 allyl 2,6-di-O-benzyl-3-O-p-methoxybenzyl-α-D-glucopyranoside 

Relevant academic research and scientific papers

The allyl group for protection in carbohydrate chemistry. XXXI conversion of allyl 2,6-di-o-benzyl-α-d-galactopyranoside into allyl 2,6-di-o-benzyl-α-d-glucopyranoside and 2,6-di-o-benzyl-d-glucopyranose

Allyl 2,6-di-O-benzyl-α-D-galactopyranoside was converted by tin-mediated alkylation into the 3-O-p-methoxybenzyl ether which gave the 4-0-mesyl derivative. Sodium benzoate in refluxing N,N-dimethylformamide converted the last compound into allyl 4-O-benz