83236-83-3

Upstream product

• 76-83-5 trityl chloride 
• 25320-99-4 benzyl α-D-glucopyranoside 

Downstream Products

• 83236-84-4 benzyl 4-O-allyl-3-O-benzyl-α-D-glucopyranoside 
• 83236-85-5 benzyl 3-O-allyl-4-O-benzyl-α-D-glucopyranoside 
• 83236-90-2 benzyl O-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-(1->2)-4-O-allyl-3-O-benzyl-α-D-glucopyranoside 
• 83236-88-8 benzyl O-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-(1->2)-4-O-allyl-6-O-benzoyl-3-O-benzyl-α-D-glucopyranoside 
• 83236-89-9 benzyl O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1->2)-4-O-allyl-6-O-benzoyl-3-O-benzyl-α-D-glucopyranoside 
• 86172-89-6 (2S,3R,4R,5R,6R)-2,4,5-Tris-benzyloxy-6-hydroxymethyl-tetrahydro-pyran-3-ol 
• 86173-10-6 Acetic acid (2S,3R,4S,5R,6R)-6-acetoxymethyl-2,4,5-tris-benzyloxy-tetrahydro-pyran-3-yl ester 

Relevant academic research and scientific papers

Ditritylation of Methyl and Benzyl α-D-Gluco-, -Manno-, and -Galactopyranosides and Preparation of Their Partially Benzylated Derivatives

The ditritylation of methyl and benzyl α-D-gluco-, -manno-, and -galactopyranosides with trityl chloride in pyridine at 70 deg C proceeds in a regioselective manner to give the 2,6-ditrityl ethers of the glucosides, the 3,6-ones of the mannosides, and bot

SYNTHESIS OF A TRIFURCATED TETRASACCHARIDE USING DEHYDRATIVE GLYCOSYLATION

2,6-Di-O-(β-D-glucopyranosyl)-4-O-(α-L-rhamnopyranosyl)-D-glucopyranose was synthesized through three successive glycosylation with the benzyl-protected glycoses starting from the glycosyl acceptor, benzyl 4-O-allyl-6-O-benzoyl-3-O-benzyl-α-D-glucopyranos