79317-18-3

Upstream product

• 55628-56-3 1,2-di-O-acetyl-3,4,6-tri-O-benzyl-α/β-D-mannopyranoside 
• 1693-71-6 tris(allyl)borate 
• 108869-64-3 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl trichloroacetimidate 
• 107-18-6 allyl alcohol 
• 16697-49-7 3,4,6-tri-O-benzyl-1,2-O-(methoxyethylidene)-β-D-mannopyranose 
• 13242-53-0 acetobromomannose 
• 55864-95-4 3,4,6-tri-O-acetyl-1,2-O-(allyloxyethylidene)-β-D-mannopyranose 
• 136944-92-8 1,2-O-(Allyloxyethyliden)-β-D-mannopyranose 
• 189324-22-9 (3aS,5R,6R,7S,7aS)-2-Allyloxy-6,7-bis-benzyloxy-5-benzyloxymethyl-2-methyl-tetrahydro-[1,3]dioxolo[4,5-b]pyran 
• 65827-59-0 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl chloride 
• 97576-67-5 (2S,3aS,5R,6R,7S,7aR)-2-Allyloxy-6,7-bis-benzyloxy-5-benzyloxymethyl-2-methyl-hexahydro-furo[3,2-b]pyran 
• 79317-17-2 (2S,3aS,5R,6R,7S,7aS)-2-Allyloxy-6,7-bis-benzyloxy-5-benzyloxymethyl-2-methyl-tetrahydro-[1,3]dioxolo[4,5-b]pyran 

Downstream Products

• 97576-68-6 (2S,3S,4R,5R,6R)-2-Allyloxy-4,5-bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-3-ol 
• 97576-71-1 3,4,6-tri-O-benzyl-2-O-chloroacetyl-α-D-mannopyranosyl chloride 
• 97576-70-0 3,4,6-tri-O-benzyl-2-O-chloroacetyl-α-D-mannopyranose 
• 97576-69-7 allyl 3,4,6-tri-O-benzyl-2-O-chloroacetyl-α-D-mannopyranoside 
• 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 
• 97576-84-6 3,4,6-tri-O-benzyl-2-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-α-D-mannopyranose 
• 136945-11-4 8-Methoxycarbonyloctyl-O-(2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1->3)-2,4,6-tri-O-benzyl-β-D-mannopyranosid 
• 136945-12-5 8-Methoxycarbonyloctyl-O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1->3)-2,4,6-tri-O-benzyl-β-D-mannopyranosid 
• 108869-64-3 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl trichloroacetimidate 
• 156719-24-3 1-O-acetyl-3,4,6-tri-O-benzyl-2-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-α-D-mannopyranose 
• 156719-23-2 allyl 3,4,6-tri-O-benzyl-2-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-α-D-mannopyranoside 
• 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 
• 97576-74-4 allyl (3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1->2)-3,4,6-tri-O-benzyl-α-D-mannopyranoside 

Relevant academic research and scientific papers

Synthesis of alkyl glycosides using trialkyl borates

Some trialkyl borates worked as highly reactive glycosyl acceptors of glycosyl acetates. Several allyl glycosides were obtained in good yields by the reaction of glycosyl acetates with triallyl borate using ytterbium(III) trifluoromethanesulfonate as the

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

Synthesis of truncated analogues for studying the process of glycosyl phosphatidylinositol modification

Figure presented Many eukaryotic proteins are modified with a glycosylphosphatidylinositol (GPI) anchor at their C-termini. This post-translational modification causes these proteins to be noncovalently tethered to the plasma membrane. The synthesis of tr

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 di- and tri-saccharides with intramolecular NH-glycosidic linkages: Molecules with flexible and rigid glycosidic bonds for conformational studies

Attempted dephthalimidation of the trisaccharide 1-O-acetyl-3,4-di-O- benzyl-2,6-di-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D- glucopyranosyl)-α-D-mannopyranose (1) and its derivatives 2 and 3, as well as the disaccharide 1-O-acetyl-3,4,6-tri-O-benz

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