338744-54-0

Downstream Products

• 188806-73-7 pent-4-enyl 3-O-benzyl-2-deoxy-2-phthalimido-4,6-di-O-trityl-β-D-glucopyranoside 
• 188806-82-8 Acetic acid (2S,3R,4S,5S,6R)-4,5-diacetoxy-6-acetoxymethyl-2-[(2R,3S,4R,5R,6R)-4-benzyloxy-5-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-6-pent-4-enyloxy-2-trityloxymethyl-tetrahydro-pyran-3-yloxy]-tetrahydro-pyran-3-yl ester 
• 188806-94-2 C₆₆H₈₁NO₃₃ 

Relevant academic research and scientific papers

A highly convergent synthesis of a hexasaccharide derived from the oligosaccharide of group B type III Streptococcus

We have developed a novel glycosylation strategy which enabled a highly convergent assembly of a hexasaccharide derived from group B type III Streptococcus.

A highly convergent synthesis of a complex oligosaccharide derived from group B type III Streptococcus

An efficient synthesis of a heptasaccharide derived from group B type III Streptococcus carrying an artificial spacer (1) is described. Rapid assembly of a protected heptasaccharide (16a) is accomplished from readily available building blocks 2-5 without a single protecting group manipulation between glycosylation steps. The synthetic strategy may be applied to the assembly of other branched complex oligosaccharides. The deprotected heptasaccharide 1 was coupled to a poly[N-(acryloyloxy)succinimide, and the resulting material will be used for the development of an ELISA assay to detect antibodies against GBS, type III in pregnant women.