79218-89-6

Upstream product

• 79218-90-9 6-O-acetyl-3,4-di-O-benzyl-1,2-O-(1-methoxyethylidene)-β-D-mannopyranose 
• 79218-92-1 1,2-O-(1-methoxyethylidene)-6-O-trityl-β-D-mannopyranose 
• 79218-91-0 3,4-di-O-benzyl-1,2-O-(1-methoxyethylidene)-6-O-trityl-β-D-mannopyramose 
• 73045-75-7 2,6-di-O-acetyl-3,4-di-O-benzyl-α-D-mannopyranosyl chloride 
• 65827-63-6 (2S,3S,4R,5R,6R)-4,5-Bis-benzyloxy-6-hydroxymethyl-tetrahydro-pyran-2,3-diol 
• 29073-91-4 (3aS,5R,6S,7aS)-5-Hydroxymethyl-2-methoxy-2-methyl-tetrahydro-[1,3]dioxolo[4,5-b]pyran-6,7-diol 
• 100-39-0 benzyl bromide 
• 65827-57-8 1,2,6-tri-O-acetyl-3,4-di-O-benzyl-α-D-mannopyranose 
• 16697-49-7 3,4,6-tri-O-benzyl-1,2-O-(methoxyethylidene)-β-D-mannopyranose 
• 86172-78-3 (2R,3S,4S,5S,6S)-6-Methoxy-5-trityloxy-2-trityloxymethyl-tetrahydro-pyran-3,4-diol 
• 86172-79-4 (2S,3S,4S,5R,6R)-2-Methoxy-4-trityloxy-6-trityloxymethyl-tetrahydro-pyran-3,5-diol 
• 81561-88-8 (2R,3R,4S,5S,6S)-3,4-Bis-benzyloxy-6-methoxy-5-trityloxy-2-trityloxymethyl-tetrahydro-pyran 
• 100-44-7 benzyl chloride 
• 73395-14-9 methyl (R,R)-2,3:4,6-di-O-benzylidene-α-D-mannopyranoside 

Downstream Products

• 147985-39-5 methyl 3,4-di-O-benzyl-2,6-di-O-benzyl-2,6-di-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimino-β-D-glucopyranosyl)-α-D-mannopyranoside 
• 57783-73-0 methyl 3,4-di-O-benzyl-α-D-mannopyranoside 

Relevant academic research and scientific papers

Borane/Bu2BOTf: A mild reagent for the regioselective reductive ring opening of benzylidene acetals in carbohydrates

BH3/Bu2OTf is an effective reagent to reductively cleave 4,6-O-benzylidene acetals of various hexopyranosides to the corresponding 4-O-benzyl ethers. 4,6-O-Isopropylidene acetals can be similarly cleaved. Common protecting groups are

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 MODEL OF AN IMMER CHAIN OF CELL-WALL PROTEOHETEROGLYCAN ISOLATED FROM Piricularia oryzae: BRANCHED D-MANNOPENTAOSIDES

Efficient syntheses are described of the branched D-mannopentaosides methyl 2,6-di-O-(2-O-α-D-mannopyranosyl-α-D-mannopyranosyl)-α-D-mannopyranoside and methyl 2,4-di-O-(2-O-α-D-mannopyranosyl-α-D-mannopyranosyl)-α-D-mannopyranoside, starting from the gly