75962-01-5

Upstream product

• 89243-32-3 allyl 3-O-allyl-2,4,6-tri-O-(p-bromboenzyl)-D-glucopyranoside 
• 89300-73-2 allyl 3-O-allyl-αβ-D-glucopyranose 
• 20316-77-2 (3aR,5R,6S,6aR)-6-(allyloxy)-5-((R)-2,2-dimethyl[1,3]dioxolan-4-yl)-2,2-dimethyl-tetrahydrofuro[2,3-d][1,3]dioxole 
• 75962-00-4 3-O-allyl-2,4,6-tri-O-(p-bromobenzyl)-α-D-mannopyranoside 
• 75962-03-7 1,3-Anhydro-2,4,6-tri-O-(p-bromobenzyl)-β-D-mannopyranose 
• 75962-02-6 2,4,6-Tri-O-(p-bromobenzyl)-D-mannopyranosyl Chloride 
• 75975-13-2 3-O-allyl-2,4,6-tri-O-(p-bromobenzyl)-D-mannopyranose 

Downstream Products

• 75962-02-6 2,4,6-Tri-O-(p-bromobenzyl)-D-mannopyranosyl Chloride 
• 89243-38-9 3-O-acetyl-2,4,6-tri-O-(p-bromobenzyl)-α-D-glucopyranosyl chloride 
• 89243-40-3 1,3-anhydro-2,4,6-tri-O-(p-bromobenzyl)-β-D-glucopyranose 
• 89243-36-7 1,3-di-O-acetyl-2,4,6-tri-O-(p-bromobenzyl)-β-D-glucopyranose 

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