97576-74-4

Upstream product

• 97576-82-4 allyl (2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1->2)-3,4,6-tri-O-benzyl-α-D-mannopyranoside 
• 79317-18-3 1-O-allyl-2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranoside 
• 108869-64-3 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl trichloroacetimidate 
• 97576-68-6 (2S,3S,4R,5R,6R)-2-Allyloxy-4,5-bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-3-ol 
• 79218-68-1 ethyl 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranoside 
• 16697-49-7 3,4,6-tri-O-benzyl-1,2-O-(methoxyethylidene)-β-D-mannopyranose 
• 65827-59-0 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl chloride 

Downstream Products

• 97576-76-6 allyl 3,4,6-tri-O-benzyl-2-O-<3,4,6-tri-O-benzyl-2-O-(2,3,4,6-tetra-O-benzyl-β-D-mannopyranosyl)-α-D-mannopyranosyl>-α-D-mannopyranoside 
• 97576-75-5 allyl 3,4,6-tri-O-benzyl-2-O-<3,4,6-tri-O-benzyl-2-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-α-D-mannopyranosyl>-α-D-mannopyranoside 
• 865179-75-5 allyl (2-O-acetyl-3,4,6-tri-O-benzyl-β-D-glucopyranosyl)-(1->2)-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1->2)-3,4,6-tri-O-benzyl-α-D-mannopyranoside 
• 1607836-58-7 C₉₈H₁₀₂O₁₈S 
• 97576-84-6 3,4,6-tri-O-benzyl-2-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-α-D-mannopyranose 
• 97576-77-7 3,4,6-tri-O-benzyl-2-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-α-D-mannopyranosyl chloride 
• 97576-83-5 allyl 3,4,6-tri-O-benzyl-2-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-α-D-mannopyranoside 

Relevant academic research and scientific papers

Intramolecular aglycon delivery for (1 → 2)-β-mannosylation: Towards the synthesis of phospholipomannan of Candida albicans

A high yielding method for 1,2-cis-β-D-mannosylation by intra-molecular aglycon delivery (IAD) through p-methoxy benzyl ether/acetal exchange and phenylsulfoxide donor is reported, along with its application in iterative assembly of antigenic (1 → 2)-β-pe

Syntheses of oligomannosides in solution and on a soluble polymer support: A comparison

The α-(1→6)-linked and the α-(1→2)-linked linear mannotetraose glycosides 3 and 4, respectively, and the branched mannopentaoside 2 [R = CH2(CH2)2CH2Cl] were synthesised by conventional methods in solution, usin

SYNTHESIS OF A BRANCHED MANNOHEXAOSIDE, A PART STRUCTURE OF A HIGH-MANNOSE-TYPE GLYCAN OF A GLYCOPROTEIN

The synthesis is described of a branched mannohexaoside derivative, propyl 6-O--α-D-mannopyranoside, which corresponds to the non-reducing-end part-structure of a high-mannose-type g