Glycosides of 8-hydroxy-3,6-dioxaoctanal. A synthesis of a new spacer for synthetic oligosaccharides.

@article{VerezBencomo1991GlycosidesO8,
  title={Glycosides of 8-hydroxy-3,6-dioxaoctanal. A synthesis of a new spacer for synthetic oligosaccharides.},
  author={vicente Verez-Bencomo and M T Campos-Valdes and J. R. Marino-albernas and Violeta Fern{\'a}ndez-Santana and M Hernandez-Rensoli and Carlos P{\'e}rez-Mart{\'i}nez},
  journal={Carbohydrate research},
  year={1991},
  volume={217},
  pages={
          263-7
        }
}
7 Citations
A method for glycoconjugate synthesis
TLDR
7-Formylheptyl glycosides of 2-acetamido-2-deoxy-β-d-glucopyranose andO-α-l-rhamnopyranosyl were synthesized and were coupled by reductive amination to bovine serum albumin and aminopropyl glass, respectively.
Synthesis of oligosaccharides with oligoethylene glycolspacers and their conversion into glycoconjugates usingN,N,N′,N′-tetramethyl(succinimido)u roniu mtetrafluoroborate as coupling reagent
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Glycosides of glucose and lactose with di- and tetraethylene glycols, transformed into bifunctional (alcohol, ester) spacer molecules, have been synthesized using tetramethyl(succinimido)uronium tetrafluoroborate for the formation of an active ester.
Synthesis of the Vibrio Cholerae O1 Ogawa and Inaba Terminal Disaccharides With Dioxolane-Type Spacers and their Coupling to Proteins1
Abstract The disaccharide, which corresponds to the terminal fragment of the Vibrio cholerae O1 LPS, was prepared starting from the corresponding trichloroacetimidate derivative of the monosaccharide
Synthesis of the Trisaccharide α-l-Rha-(1-2)-α-l-Rha-(1-2)-α-L-Rha with a Dioxolane-Type Spacer-Arm1
Abstract The trisaccharide α-L-Rha-(1-2)-α-L-Rha-(1-2)-α-L-Rha with a dioxolane-type spacer was obtained by using the trichloroacetimidate method in all of the glycosidation steps. After

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