852568-11-7

Upstream product

• 141342-83-8 phenyl 6-O-benzyl-2-deoxy-2-phthalimido-1-thio-1-deoxy-β-D-glucopyranoside 

Downstream Products

• 852568-12-8 C₆₃H₅₇ClFNO₁₉ 
• 852568-18-4 C₆₈H₆₇ClN₄O₂₀ 
• 852568-17-3 Benzoic acid (2S,4aR,6S,7R,8S,8aS)-6-[(2R,3S,4R,5R,6R)-6-(5-azido-pentyloxy)-2-benzyloxymethyl-5-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-4-hydroxy-tetrahydro-pyran-3-yloxy]-8-(2-chloro-acetoxy)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl ester 

Relevant academic research and scientific papers

Efficient polymer-assisted strategy for the deprotection of protected oligosaccharides

(Chemical Equation Presented) New strategies in sugar synthesis: A prelinker containing a dihydropyranyl moiety and an activated ester can be attached to a sugar, which is then loaded onto an amino-modified support by amidation. Standard protecting-group manipulations are possible. Final cleavage of the linker under mildly acidic conditions provides the fully deprotected oligosaccharides. TFA=trifluoroacetic acid.

Automated parallel synthesis of a protected oligosaccharride library based upon the structure of dimeric Lewis X by one-pot sequential glycosylation

An efficient synthesis of a protected dimeric Lewis X epitope by two sequential one-pot glycosylations is described. Combinatorial synthesis of the dimeric Lewis X epitope derivatives by the one-pot glycosylation was accomplished utilizing an automated synthesizer to provide 12-protected oligosaccharides.