75962-03-7

Upstream product

• 75962-02-6 2,4,6-Tri-O-(p-bromobenzyl)-D-mannopyranosyl Chloride 
• 84553-81-1 3-O-acetyl-2,4,6-tri-O-(p-bromobenzyl)-α-D-mannopyranosyl chloride 
• 84553-80-0 methyl 3-O-acetyl-2,4,6-tri-O-(p-bromobenzyl)-α-D-mannopyranoside 

Downstream Products

• 75962-00-4 3-O-allyl-2,4,6-tri-O-(p-bromobenzyl)-α-D-mannopyranoside 
• 75975-13-2 3-O-allyl-2,4,6-tri-O-(p-bromobenzyl)-D-mannopyranose 
• 75962-01-5 2,4,6-Tri-O-(p-bromobenzyl)-D-mannopyranose 

Relevant academic research and scientific papers

Synthesis of Substituted 2,6-Dioxabicycloheptanes. 1,3-Anhydro-2,4,6-tri-O-benzyl- and 1,3-Anhydro-2,4,6-tri-O-(p-bromobenzyl)-β-D-mannopyranose

The title compounds 1,3-anhydro-2,4,6-tri-O-benzyl- and 1,3-anhydro-2,4,6-tri-O-(p-brombenzyl)-β-D-mannopyranose were synthesized by a reaction sequence involving blocking the C-3 hydroxyl with an allyl group by first forming a dibutylstannylene complex b