144367-30-6Relevant academic research and scientific papers
Sugars within a hydrophobic scaffold: Glycodendrimers from polyphenylenes
Sakamoto, Junji,Muellen, Klaus
, p. 4277 - 4280 (2007/10/03)
(Chemical Equation Presented) A new glycodendrimer type has been introduced that is designed on the basis of shape-persistent polyphenylene dendrimers. The sugar installation occurs not only on the dendrimer surface but also within the hydrophobic internal scaffold. The synthesis has been accomplished via both convergent and divergent routes by employing the Schmidt glycosylation and the Diels-Alder reaction. This new glycodendrimer has been found to exhibit water-solubility, while conserving hydrophobicity of the interior environment despite the incorporation of sugars.
Synthesis of hyaluronic acid-related di-, tri-, and tetra-saccharides having an N-acetylglucosamine residue at the reducing end
Slaghek,Nakahara,Ogawa,Kamerling,Vliegenthart
, p. 61 - 85 (2007/10/02)
The synthesis is reported of 4-methoxyphenyl O-(β-D-glucopyranosyluronic acid)-(1 → 3)-2-acetamido-2-deoxy β-D-glucopyranoside (1), 4-methoxyphenyl O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1 → 4)-O-(β-D-glucopyranosyluronic acid)-(1 → 3)-2-acetamido-2-
