93381-66-9

Upstream product

• 76-83-5 trityl chloride 
• 41308-76-3 allyl α-D-mannopyranoside 
• 83-87-4 D-Mannose pentaacetate 
• 530-26-7 D-Mannose 
• 3458-28-4 D-Mannose 
• 119111-31-8 allyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside 

Downstream Products

• 97205-13-5 allyl 2-O-allyl-6-O-trityl-α-D-mannopyranoside 
• 93298-40-9 allyl 3-O-allyl-6-O-trityl-α-D-mannopyranoside 
• 84620-68-8 3-O-acetyl-2,4,6-tri-O-benzyl-α-D-mannopyranosyl acetate 
• 84553-84-4 2,4,6-tri-O-benzyl-α-D-mannopyranose 
• 93381-68-1 allyl 3-O-allyl-2,4,6-tri-O-benzyl-α-D-mannopyranoside 
• 239803-12-4 [(2R,3R,4R,5S,6S)-6-Allyloxy-5-benzyloxy-4-(4-methoxy-benzyloxy)-2-trityloxymethyl-tetrahydro-pyran-3-yloxy]-tert-butyl-diphenyl-silane 
• 239803-09-9 (2S,3S,4R,5R,6R)-2-Allyloxy-3-benzyloxy-4-(tert-butyl-dimethyl-silanyloxy)-5-(tert-butyl-diphenyl-silanyloxy)-6-trityloxymethyl-tetrahydro-pyran 
• 239803-07-7 (2S,3S,4R,5R,6R)-2-Allyloxy-5-(tert-butyl-diphenyl-silanyloxy)-4-(4-methoxy-benzyloxy)-6-trityloxymethyl-tetrahydro-pyran-3-ol 
• 239803-06-6 [(3aS,4S,6R,7R,7aR)-4-Allyloxy-2-(4-methoxy-phenyl)-6-trityloxymethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-7-yloxy]-tert-butyl-diphenyl-silane 
• 239803-08-8 (2S,3S,4R,5S,6R)-2-Allyloxy-3-benzyloxy-5-(tert-butyl-diphenyl-silanyloxy)-6-trityloxymethyl-tetrahydro-pyran-4-ol 
• 534574-87-3 2,3,4-tri-O-benzyl-1-O-(2-propenyl)-6-O-(4-tolylsulfonyl)-α-D-mannose 
• 603961-98-4 allyl 2,3,4-tri-O-benzyl-α-D-rhamnopyranoside 
• 93451-42-4 allyl 6-O-acetyl-2,3,4-tri-O-benzyl-α-D-mannopyranoside 

Relevant academic research and scientific papers

Automated Solution-Phase Synthesis of S-Glycosides for the Production of Oligomannopyranoside Derivatives

Thioglycosides are more resistant to enzymatic hydrolysis than their O-linked counterparts, thereby becoming attractive targets for carbohydrate-based therapeutic development. We report the first development of methods for the site-selective incorporation

Total synthesis of the fully lipidated glycosylphosphatidylinositol (GPI) anchor of malarial parasite Plasmodium falciparum

We report a new and convergent strategy for the total synthesis of fully lipidated glycosylphosphatidylinositol (GPI) anchor, the major pro-inflammatory factor of malarial parasite (Plasmodium falciparum). The key features of our approach include, the acc

A new approach to construct full-length glycosylphosphatidylinositols of parasitic protozoa and [4-deoxy-Man-III]-GPI analogues

A new [2 + 2 + 2] approach to construct GPI molecules through the efficient synthesis of glucosamine-inositol and tetramannose intermediates led to a total synthesis of a GPI-anchor of Trypanosoma cruzi, and also afforded a key intermediate for the synthe

Efficient and practical syntheses of three pentasaccharides core structures corresponding to N-glycans

Three branched pentasaccharide derivatives and one tetrasaccharide were synthesized efficiently. The advantages of this method include a one-pot facile synthesis of 3,6-differentially protected mannose building block and an efficient strategy for oligosac

A practical synthetic method for α- and β-glycosyloxyacetic acids

Dihydroxylation of allyl 2,3,4-tri-O-benzyl-6-O-tritylglycosides provides diols, the anomers of which can easily be separated by column chromatography in a practical scale. These anomers can be cleanly transformed into α- and β-glycosyloxyacetic acids, respectively, via oxidative cleavage of the diol followed by oxidation.

Highly efficient and practical synthesis of 3,6-branched oligosaccharides.

[reaction: see text] A one-pot formation of the 3- and 6-OH differentially protected sugar synthon was described. A mannopyranosyl pentasaccharide and a glucopyranosyl hexasaccharide were prepared employing this new finding.

SYNTHESIS OF A MODEL, LINEAR D-MANNOPENTAOSE FOR THE NONREDUCING-END SEQUENCE OF THE CELL-SURFACE D-MANNAN OF Escherichia coli, Candida albicans, AND Saccharomyces cerevisiae

Synthesis, in a regio- and stereocontrolled way, of a linear D-manno-oligosaccharide, namely, O-α-Man-(1--3)-O-α-Man-(1--2)-O-α-Man-(1--2)-α-Man-(1--2)-α-Man, which corresponds to a part of the structure of the cell-surface D-mannan of Escherichia coli, C