Literature DB >> 15524462

Sugars within a hydrophobic scaffold: glycodendrimers from polyphenylenes.

Junji Sakamoto1, Klaus Müllen.   

Abstract

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.

Entities:  

Year:  2004        PMID: 15524462     DOI: 10.1021/ol048282l

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

Review 1.  Design and creativity in synthesis of multivalent neoglycoconjugates.

Authors:  Yoann M Chabre; René Roy
Journal:  Adv Carbohydr Chem Biochem       Date:  2010       Impact factor: 12.200

2.  Hexaphenylbenzene as a rigid template for the straightforward syntheses of "star-shaped" glycodendrimers.

Authors:  Yoann M Chabre; Patrick P Brisebois; Leïla Abbassi; Sheena C Kerr; John V Fahy; Isabelle Marcotte; René Roy
Journal:  J Org Chem       Date:  2010-12-29       Impact factor: 4.354

Review 3.  Analysis of carbohydrates and glycoconjugates by matrix-assisted laser desorption/ionization mass spectrometry: An update for 2003-2004.

Authors:  David J Harvey
Journal:  Mass Spectrom Rev       Date:  2009 Mar-Apr       Impact factor: 10.946

  3 in total

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