77388-92-2

Upstream product

• 100-44-7 benzyl chloride 
• 89300-73-2 allyl 3-O-allyl-αβ-D-glucopyranose 

Downstream Products

• 77388-93-3 1-propenyl 2,4,6-tri-O-benzyl-3-O-(1-propenyl)-α-D-glucopyranose 
• 37111-85-6 2,4,6-tri-O-benzyl-D-glucopyranose 
• 77388-96-6 2,4,6-tri-O-benzyl-α-D-glucopyranosyl chloride 
• 76543-11-8 1,3-anhydro-2,4,6-tri-O-benzyl-β-D-glucopyranose 
• 77388-97-7 1,5-anhydro-2,4,6-tri-O-benzyl-D-arabino-hex-1-enitol 
• 33208-48-9 1,6 anhydro-2,4-di-O-benzyl-β-D-glucopyranose 

Relevant academic research and scientific papers

SYNTHESIS OF A SUBSTITUTED 2,6-DIOXABICYCLOHEPTANE, 1,3-ANHYDRO-2,4,6-TRI-O-BENZYL-β-D-GLUCOPYRANOSE

1,3-Anhydro-2,4,6-tri-O-benzyl-β-D-glucopyranose has been synthesized by ring closure of 2,4,6-tri-O-benzyl-α-D-glucopyranosyl chloride via two reaction sequences.The preferable method has allyl 3-O-allyl D-glucopyranoside as key intermediate.This appears to be the first example of an anhydro sugar derivative with the 2,6-dioxabicycloheptane skeleton.